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24 - HIV-related lymphomas

Published online by Cambridge University Press:  10 January 2011

Caroline M. Behler
Affiliation:
San Francisco Veterans Affairs Medical Center, 4150 Clement Street, 111H1, San Francisco, CA, USA
Lawrence D. Kaplan
Affiliation:
Division of Hematology/Oncology, University of California San Francisco, CA, USA
Susan O'Brien
Affiliation:
University of Texas/MD Anderson Cancer Center, Houston
Julie M. Vose
Affiliation:
University of Nebraska Medical Center, Omaha
Hagop M. Kantarjian
Affiliation:
University of Texas/MD Anderson Cancer Center, Houston
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Summary

Epidemiology/etiology

Ever since the beginning of the HIV/AIDS pandemic, it has been recognized that in addition to the increased risk of opportunistic and other infections, the incidence of malignancy is much greater in people with HIV/AIDS (PWHA) than that of the general population. This risk is likely a direct result of the immune dysfunction from chronic HIV infection, though concomitant viral infections including Epstein–Barr virus (EBV), human herpesvirus 8 (HHV-8), and human papilloma virus (HPV) also play a role. While the incidence of cancers is increased both for PWHA and immunosuppressed organ transplant patients, the risk of non-Hodgkin (NHL) and Hodgkin (HL) lymphomas appears to be significantly greater in the setting of HIV/AIDS compared to the transplant population.

This risk of NHL is 25- to 200-fold increased in PWHA compared to those without HIV, and risk appears to increase with duration of HIV infection as well as with lower CD4 counts. The risk of HL, while not considered an AIDS-defining illness (ADI) by the Centers for Disease Control, is increased by about 5- to 15-fold in PWHA; however, its incidence is decreased with lower CD4 counts. Since the widespread introduction of highly active antiretroviral therapy (HAART) in the mid-1990s, the incidence of ADIs and mortality among PWHA has decreased dramatically and many studies have reported an increase in the proportion of ADIs attributable to HIV-related lymphomas (HRL).

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Publisher: Cambridge University Press
Print publication year: 2010

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References

Grulich, AE, Leeuwen, MT, Falster, MO, et al. Incidence of cancers in people with HIV/AIDS compared with immunosuppressed transplant recipients: a meta-analysis. Lancet 2007;370(9581):59–67.CrossRefGoogle ScholarPubMed
Serraino, D, Piselli, P, Busnach, G, et al. Risk of cancer following immunosuppression in organ transplant recipients and in HIV-positive individuals in southern Europe. Eur J Cancer 2007;43(14):2117–23.CrossRefGoogle ScholarPubMed
Rabkin, CS, Hilgartner, MW, Hedberg, KW, et al. Incidence of lymphomas and other cancers in HIV-infected and HIV-uninfected patients with hemophilia. JAMA 1992;267(8):1090–4.CrossRefGoogle ScholarPubMed
Goedert, JJ, Cote, TR, Virgo, P, et al. Spectrum of AIDS-associated malignant disorders. Lancet 1998;351(9119):1833–9.CrossRefGoogle ScholarPubMed
Biggar, RJ, Kirby, KA, Atkinson, J, et al. Cancer risk in elderly persons with HIV/AIDS. J Acquir Immune Defic Syndr 2004;36(3):861–8.CrossRefGoogle ScholarPubMed
Serraino, D, Boschini, A, Carrieri, P, et al. Cancer risk among men with, or at risk of, HIV infection in southern Europe. AIDS 2000;14(5):553–9.CrossRefGoogle ScholarPubMed
Munoz, A, Schrager, LK, Bacellar, H, et al. Trends in the incidence of outcomes defining acquired immunodeficiency syndrome (AIDS) in the Multicenter AIDS Cohort Study: 1985–1991. Am J Epidemiol 1993;137(4):423–38.CrossRefGoogle ScholarPubMed
Pluda, JM, Venzon, DJ, Tosato, G, et al. Parameters affecting the development of non-Hodgkin's lymphoma in patients with severe human immunodeficiency virus infection receiving antiretroviral therapy. J Clin Oncol 1993;11(6):1099–107.CrossRefGoogle ScholarPubMed
Kirk, O, Pedersen, C, Cozzi-Lepri, A, et al. Non-Hodgkin lymphoma in HIV-infected patients in the era of highly active antiretroviral therapy. Blood 2001;98(12):3406–12.CrossRefGoogle ScholarPubMed
Hessol, NA, Katz, MH, Liu, JY, et al. Increased incidence of Hodgkin disease in homosexual men with HIV infection. Ann Intern Med 1992;117(4):309–11.CrossRefGoogle ScholarPubMed
Frisch, M, Biggar, RJ, Engels, EA, et al. Association of cancer with AIDS-related immunosuppression in adults. JAMA 2001;285(13):1736–45.CrossRefGoogle ScholarPubMed
Grulich, AE, Li, Y, McDonald, A, et al. Rates of non-AIDS-defining cancers in people with HIV infection before and after AIDS diagnosis. AIDS 2002;16(8):1155–61.CrossRefGoogle ScholarPubMed
Biggar, RJ, Jaffe, ES, Goedert, JJ, et al. Hodgkin lymphoma and immunodeficiency in persons with HIV/AIDS. Blood 2006;108(12):3786–91.CrossRefGoogle ScholarPubMed
Palella, FJ, Delaney, KM, Moorman, AC, et al. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. HIV Outpatient Study Investigators. N Engl J Med 1998;338(13):853–60.CrossRefGoogle ScholarPubMed
Mocroft, A, Katlama, C, Johnson, AM, et al. AIDS across Europe, 1994–98: the EuroSIDA study. Lancet 2000;356(9226):291–6.CrossRefGoogle ScholarPubMed
Matthews, GV, Bower, M, Mandalia, S, et al. Changes in acquired immunodeficiency syndrome-related lymphoma since the introduction of highly active antiretroviral therapy. Blood 2000;96(8):2730–4.Google ScholarPubMed
Dore, GJ, Li, Y, McDonald, A, et al. Impact of highly active antiretroviral therapy on individual AIDS-defining illness incidence and survival in Australia. J Acquir Immune Defic Syndr 2002;29(4):388–95.CrossRefGoogle ScholarPubMed
Gates, AE, Kaplan, LD. Biology and management of AIDS-associated non-Hodgkin's lymphoma. Hematol Oncol Clin North Am 2003;17(3):821–41.CrossRefGoogle ScholarPubMed
Besson, C, Goubar, A, Gabarre, J, et al. Changes in AIDS-related lymphoma since the era of highly active antiretroviral therapy. Blood 2001;98(8):2339–44.CrossRefGoogle ScholarPubMed
Bonnet, F, Balestre, E, Thiebaut, R, et al. Factors associated with the occurrence of AIDS-related non-Hodgkin lymphoma in the era of highly active antiretroviral therapy: Aquitaine Cohort, France. Clin Infect Dis 2006;42(3):411–17.CrossRefGoogle ScholarPubMed
Diamond, C, Taylor, TH, Aboumrad, T, et al. Changes in acquired immunodeficiency syndrome-related non-Hodgkin lymphoma in the era of highly active antiretroviral therapy: incidence, presentation, treatment, and survival. Cancer 2006;106(1):128–35.CrossRefGoogle Scholar
Polesel, J, Clifford, GM, Rickenbach, M, et al. Non-Hodgkin lymphoma incidence in the Swiss HIV Cohort Study before and after highly active antiretroviral therapy. AIDS 2008;22(2):301–6.CrossRefGoogle ScholarPubMed
Engels, EA, Pfeiffer, RM, Goedert, JJ, et al. Trends in cancer risk among people with AIDS in the United States 1980–2002. AIDS 2006;20(12):1645–54.CrossRefGoogle Scholar
Clifford, GM, Polesel, J, Rickenbach, M, et al. Cancer risk in the Swiss HIV Cohort Study: associations with immunodeficiency, smoking, and highly active antiretroviral therapy. J Natl Cancer Inst 2005;97(6):425–32.CrossRefGoogle ScholarPubMed
Silverberg, MJ, Neuhaus, J, Bower, M, et al. Risk of cancers during interrupted antiretroviral therapy in the SMART study. AIDS 2007;21(14):1957–63.CrossRefGoogle ScholarPubMed
Levine, AM, Seneviratne, L, Espina, BM, et al. Evolving characteristics of AIDS-related lymphoma. Blood 2000;96(13): 4084–90.Google ScholarPubMed
Raphael, M, Borisch, B, Jaffe, ES.Immunodeficiency associated lymphoproliferative disorders. In: Jaffe, ES, Harris, NL, Stein, H, et al., eds. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. Lyon, France, IRC Press. 2001; 255–71.Google Scholar
Kaplan, LD, Abrams, DI, Feigal, E, et al. AIDS-associated non-Hodgkin's lymphoma in San Francisco. JAMA 1989;261(5):719–24.CrossRefGoogle ScholarPubMed
Kaplan, LD, Straus, DJ, Testa, MA, et al. Low-dose compared with standard-dose m-BACOD chemotherapy for non-Hodgkin's lymphoma associated with human immunodeficiency virus infection. National Institute of Allergy and Infectious Diseases AIDS Clinical Trials Group. N Engl J Med 1997;336(23):1641–8.CrossRefGoogle ScholarPubMed
Levine, AM, Sullivan-Halley, J, Pike, MC, et al. Human immunodeficiency virus-related lymphoma. Prognostic factors predictive of survival. Cancer 1991;68(11):2466–72.3.0.CO;2-G>CrossRefGoogle Scholar
Gisselbrecht, C, Oksenhendler, E, Tirelli, U, et al. Human immunodeficiency virus-related lymphoma treatment with intensive combination chemotherapy. French-Italian Cooperative Group. Am J Med 1993;95(2):188–96.CrossRefGoogle ScholarPubMed
Vaccher, E, Tirelli, U, Spina, M, et al. Age and serum lactate dehydrogenase level are independent prognostic factors in human immunodeficiency virus-related non-Hodgkin's lymphomas: a single-institute study of 96 patients. J Clin Oncol 1996;14(8):2217–23.CrossRefGoogle ScholarPubMed
Straus, DJ, Huang, J, Testa, MA, et al. Prognostic factors in the treatment of human immunodeficiency virus-associated non-Hodgkin's lymphoma: analysis of AIDS Clinical Trials Group protocol 142–low-dose versus standard-dose m-BACOD plus granulocyte-macrophage colony-stimulating factor. National Institute of Allergy and Infectious Diseases. J Clin Oncol 1998;16(11):3601–6.CrossRefGoogle Scholar
Rossi, G, Donisi, A, Casari, S, et al. The International Prognostic Index can be used as a guide to treatment decisions regarding patients with human immunodeficiency virus-related systemic non-Hodgkin lymphoma. Cancer 1999;86(11):2391–7.3.0.CO;2-0>CrossRefGoogle ScholarPubMed
,The International Non-Hodgkin's Lymphoma Prognostic Factors Project. A predictive model for aggressive non-Hodgkin's lymphoma. N Engl J Med 1993;329(14):987–94.CrossRefGoogle Scholar
Navarro, JT, Ribera, JM, Oriol, A, et al. International prognostic index is the best prognostic factor for survival in patients with AIDS-related non-Hodgkin's lymphoma treated with CHOP. A multivariate study of 46 patients. Haematologica 1998;83(6): 508–13.Google Scholar
Bower, M, Gazzard, B, Mandalia, S, et al. A prognostic index for systemic AIDS-related non-Hodgkin lymphoma treated in the era of highly active antiretroviral therapy. Ann Intern Med 2005;143(4):265–73.CrossRefGoogle ScholarPubMed
Vaccher, E, Spina, M, Talamini, R, et al. Improvement of systemic human immunodeficiency virus-related non-Hodgkin lymphoma outcome in the era of highly active antiretroviral therapy. Clin Infect Dis 2003;37(11):1556–64.CrossRefGoogle ScholarPubMed
Lim, ST, Karim, R, Tulpule, A, et al. Prognostic factors in HIV-related diffuse large-cell lymphoma: before versus after highly active antiretroviral therapy. J Clin Oncol 2005;23(33):8477–82.CrossRefGoogle ScholarPubMed
Navarro, JT, Lloveras, N, Ribera, JM, et al. The prognosis of HIV-infected patients with diffuse large B-cell lymphoma treated with chemotherapy and highly active antiretroviral therapy is similar to that of HIV-negative patients receiving chemotherapy. Haematologica 2005;90(5):704–6.Google ScholarPubMed
Tam, HK, Zhang, ZF, Jacobson, LP, et al. Effect of highly active antiretroviral therapy on survival among HIV-infected men with Kaposi sarcoma or non-Hodgkin lymphoma. Int J Cancer 2002;98(6):916–22.CrossRefGoogle ScholarPubMed
Ribera, JM, Navarro, JT, Oriol, A, et al. Prognostic impact of highly active antiretroviral therapy in HIV-related Hodgkin's disease. AIDS 2002;16(14):1973–6.CrossRefGoogle ScholarPubMed
Gerard, L, Galicier, L, Boulanger, E, et al. Improved survival in HIV-related Hodgkin's lymphoma since the introduction of highly active antiretroviral therapy. AIDS 2003;17(1):81–7.CrossRefGoogle ScholarPubMed
Hentrich, M, Maretta, L, Chow, KU, et al. Highly active antiretroviral therapy (HAART) improves survival in HIV-associated Hodgkin's disease: results of a multicenter study. Ann Oncol 2006;17(6):914–19.CrossRefGoogle ScholarPubMed
Kaplan, LD, Lee, JY, Ambinder, RF, et al. Rituximab does not improve clinical outcome in a randomized phase 3 trial of CHOP with or without rituximab in patients with HIV-associated non-Hodgkin lymphoma: AIDS-Malignancies Consortium Trial 010. Blood 2005;106(5):1538–43.CrossRefGoogle ScholarPubMed
Little, RF, Pittaluga, S, Grant, N, et al. Highly effective treatment of acquired immunodeficiency syndrome-related lymphoma with dose-adjusted EPOCH: impact of antiretroviral therapy suspension and tumor biology. Blood 2003;101(12):4653–9.CrossRefGoogle ScholarPubMed
Lascaux, AS, Hemery, F, Goujard, C, et al. Beneficial effect of highly active antiretroviral therapy on the prognosis of AIDS-related systemic non-Hodgkin lymphomas. AIDS Res Hum Retroviruses 2005;21(3):214–20.CrossRefGoogle ScholarPubMed
Miralles, P, Berenguer, J, Ribera, JM, et al. Prognosis of AIDS-related systemic non-Hodgkin lymphoma treated with chemotherapy and highly active antiretroviral therapy depends exclusively on tumor-related factors. J Acquir Immune Defic Syndr 2007;44(2):167–73.CrossRefGoogle ScholarPubMed
Lim, ST, Karim, R, Nathwani, BN, et al. AIDS-related Burkitt's lymphoma versus diffuse large-cell lymphoma in the pre-highly active antiretroviral therapy (HAART) and HAART eras: significant differences in survival with standard chemotherapy. J Clin Oncol 2005;23(19):4430–8.CrossRefGoogle ScholarPubMed
Spina, M, Simonelli, C, Talamini, R, et al. Patients with HIV with Burkitt's lymphoma have a worse outcome than those with diffuse large-cell lymphoma also in the highly active antiretroviral therapy era. J Clin Oncol 2005;23(31):8132–3; author reply 8133–4.CrossRefGoogle ScholarPubMed
Mackall, CL, Fleisher, TA, Brown, MR, et al. Lymphocyte depletion during treatment with intensive chemotherapy for cancer. Blood 1994;84(7):2221–8.Google ScholarPubMed
Cheson, BD. Infectious and immunosuppressive complications of purine analog therapy. J Clin Oncol 1995;13(9):2431–48.CrossRefGoogle ScholarPubMed
Hakim, FT, Cepeda, R, Kaimei, S, et al. Constraints on CD4 recovery postchemotherapy in adults: thymic insufficiency and apoptotic decline of expanded peripheral CD4 cells. Blood 1997;90(9):3789–98.Google ScholarPubMed
Powles, T, Imami, N, Nelson, M, et al. Effects of combination chemotherapy and highly active antiretroviral therapy on immune parameters in HIV-1 associated lymphoma. AIDS 2002;16(4):531–6.CrossRefGoogle ScholarPubMed
Ratner, L, Lee, J, Tang, S, et al. Chemotherapy for human immunodeficiency virus-associated non-Hodgkin's lymphoma in combination with highly active antiretroviral therapy. J Clin Oncol 2001;19(8):2171–8.CrossRefGoogle ScholarPubMed
Tosi, P, Gherlinzoni, F, Visani, G, et al. AZT plus methotrexate in HIV-related non-Hodgkin's lymphomas. Leuk Lymphoma 1998;30(1–2):175–9.CrossRefGoogle ScholarPubMed
Smith, PF, DiCenzo, R, Morse, GD. Clinical pharmacokinetics of non-nucleoside reverse transcriptase inhibitors. Clin Pharmacokinet 2001;40(12):893–905.CrossRefGoogle ScholarPubMed
Chiba, M, Nishime, JA, Lin, JH. Potent and selective inactivation of human liver microsomal cytochrome P-450 isoforms by L-754,394, an investigational human immune deficiency virus protease inhibitor. J Pharmacol Exp Ther 1995;275(3):1527–34.Google ScholarPubMed
Bower, M, McCall-Peat, N, Ryan, N, et al. Protease inhibitors potentiate chemotherapy-induced neutropenia. Blood 2004;104(9):2943–6.CrossRefGoogle ScholarPubMed
Spina, M, Gabarre, J, Rossi, G, et al. Stanford V regimen and concomitant HAART in 59 patients with Hodgkin disease and HIV infection. Blood 2002;100(6):1984–8.CrossRefGoogle Scholar
Makinson, A, Martelli, N, Peyriere, H, et al. Profound neutropenia resulting from interaction between antiretroviral therapy and vinblastine in a patient with HIV-associated Hodgkin's disease. Eur J Haematol 2007;78(4):358–60.CrossRefGoogle Scholar
Moore, DA, Benepal, T, Portsmouth, S, et al. Etiology and natural history of neutropenia in human immunodeficiency virus disease: a prospective study. Clin Infect Dis 2001;32(3):469–75.CrossRefGoogle ScholarPubMed
Seneviratne, L, Espina, BM, Nathwani, BN, et al. Clinical, immunologic, and pathologic correlates of bone marrow involvement in 291 patients with acquired immunodeficiency syndrome-related lymphoma. Blood 2001;98(8):2358–63.CrossRefGoogle ScholarPubMed
Mounier, N, Spina, M, Gabarre, J, et al. AIDS-related non-Hodgkin lymphoma: final analysis of 485 patients treated with risk-adapted intensive chemotherapy. Blood 2006;107(10):3832–40.CrossRefGoogle ScholarPubMed
Boue, F, Gabarre, J, Gisselbrecht, C, et al. Phase II trial of CHOP plus rituximab in patients with HIV-associated non-Hodgkin's lymphoma. J Clin Oncol 2006;24(25):4123–8.CrossRefGoogle ScholarPubMed
Grogg, KL, Miller, RF, Dogan, A. HIV infection and lymphoma. J Clin Pathol 2007;60(12):1365–72.CrossRefGoogle ScholarPubMed
Carbone, A, Gaidano, G, Gloghini, A, et al. Differential expression of BCL-6, CD138/syndecan-1, and Epstein-Barr virus-encoded latent membrane protein-1 identifies distinct histogenetic subsets of acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas. Blood 1998;91(3):747–55.Google ScholarPubMed
MacMahon, EM, Glass, JD, Hayward, SD, et al. Epstein-Barr virus in AIDS-related primary central nervous system lymphoma. Lancet 1991;338(8773):969–73.CrossRefGoogle ScholarPubMed
Jaffe, ES, Harris, NL, Stein, H, et al. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. Lyon; Oxford: IARC Press; Oxford University Press (distributor); 2001.Google Scholar
Raphael, MM, Audouin, J, Lamine, M, et al. Immunophenotypic and genotypic analysis of acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas. Correlation with histologic features in 36 cases. French Study Group of Pathology for HIV-Associated Tumors. Am J Clin Pathol 1994;101(6):773–82.CrossRefGoogle Scholar
Hamilton-Dutoit, SJ, Rea, D, Raphael, M, et al. Epstein-Barr virus-latent gene expression and tumor cell phenotype in acquired immunodeficiency syndrome-related non-Hodgkin's lymphoma. Correlation of lymphoma phenotype with three distinct patterns of viral latency. Am J Pathol 1993;143(4):1072–85.Google ScholarPubMed
Engels, EA, Rosenberg, PS, Frisch, M, et al. Cancers associated with Kaposi's sarcoma (KS) in AIDS: a link between KS herpesvirus and immunoblastic lymphoma. Br J Cancer 2001;85(9):1298–303.CrossRefGoogle ScholarPubMed
Cioc, AM, Allen, C, Kalmar, JR, et al. Oral plasmablastic lymphomas in AIDS patients are associated with human herpesvirus 8. Am J Surg Pathol 2004;28(1):41–6.CrossRefGoogle ScholarPubMed
Deloose, ST, Smit, , Pals, FT, et al. High incidence of Kaposi sarcoma-associated herpesvirus infection in HIV-related solid immunoblastic/plasmablastic diffuse large B-cell lymphoma. Leukemia 2005;19(5):851–5.CrossRefGoogle ScholarPubMed
Castillo, J, Pantanowitz, L, Dezube, BJ. HIV-associated plasmablastic lymphoma: lessons learned from 112 published cases. Am J Hematol 2008;83(10):804–9.CrossRefGoogle ScholarPubMed
Riedel, DJ, Gonzalez-Cuyar, LF, Zhao, XF, et al. Plasmablastic lymphoma of the oral cavity: a rapidly progressive lymphoma associated with HIV infection. Lancet Infect Dis 2008;8(4):261–7.CrossRefGoogle ScholarPubMed
Simonitsch-Klupp, I, Hauser, I, Ott, G, et al. Diffuse large B-cell lymphomas with plasmablastic/plasmacytoid features are associated with TP53 deletions and poor clinical outcome. Leukemia 2004;18(1):146–55.CrossRefGoogle ScholarPubMed
Gaidano, G, Cerri, M, Capello, D, et al. Molecular histogenesis of plasmablastic lymphoma of the oral cavity. Br J Haematol 2002;119(3):622–8.CrossRefGoogle ScholarPubMed
Levine, AM, Tulpule, A, Espina, B, et al. Liposome-encapsulated doxorubicin in combination with standard agents (cyclophosphamide, vincristine, prednisone) in patients with newly diagnosed AIDS-related non-Hodgkin's lymphoma: results of therapy and correlates of response. J Clin Oncol 2004;22(13):2662–70.CrossRefGoogle Scholar
Wilson, WH, Grossbard, ML, Pittaluga, S, et al. Dose-adjusted EPOCH chemotherapy for untreated large B-cell lymphomas: a pharmacodynamic approach with high efficacy. Blood 2002;99(8):2685–93.CrossRefGoogle ScholarPubMed
Sparano, JA, Lee, S, Chen, MG, et al. Phase II trial of infusional cyclophosphamide, doxorubicin, and etoposide in patients with HIV-associated non-Hodgkin's lymphoma: an Eastern Cooperative Oncology Group Trial (E1494). J Clin Oncol 2004;22(8):1491–500.CrossRefGoogle Scholar
Sparano, JA, Wiernik, PH, Strack, M, et al. Infusional cyclophosphamide, doxorubicin, and etoposide in human immunodeficiency virus- and human T-cell leukemia virus type I-related non-Hodgkin's lymphoma: a highly active regimen. Blood 1993;81(10): 2810–15.Google ScholarPubMed
Coiffier, B, Lepage, E, Briere, J, et al. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. N Engl J Med 2002;346(4):235–42.CrossRefGoogle ScholarPubMed
Spina, M, Jaeger, U, Sparano, JA, et al. Rituximab plus infusional cyclophosphamide, doxorubicin, and etoposide in HIV-associated non-Hodgkin lymphoma: pooled results from 3 phase 2 trials. Blood 2005;105(5):1891–7.CrossRefGoogle ScholarPubMed
Ribera, JM, Oriol, A, Morgades, M, et al. Safety and efficacy of cyclophosphamide, adriamycin, vincristine, prednisone and rituximab in patients with human immunodeficiency virus-associated diffuse large B-cell lymphoma: results of a phase II trial. Br J Haematol 2008; 140(4):411–19.CrossRefGoogle ScholarPubMed
Levine, AM, Lee, J, Kaplan, L, et al. Efficacy and toxicity of concurrent rituximab plus infusional EPOCH in HIV-associated lymphoma: AIDS Malignancy Consortium Trial 034. J Clin Oncol 2008;26:Abstract 8527.CrossRefGoogle Scholar
Cabanillas, F, Liboy, I, Pavia, O, et al. High incidence of non-neutropenic infections induced by rituximab plus fludarabine and associated with hypogammaglobulinemia: a frequently unrecognized and easily treatable complication. Ann Oncol 2006;17(9):1424–7.CrossRefGoogle ScholarPubMed
Nishio, M, Fujimoto, K, Yamamoto, S, et al. Hypogammaglobulinemia with a selective delayed recovery in memory B cells and an impaired isotype expression after rituximab administration as an adjuvant to autologous stem cell transplantation for non-Hodgkin lymphoma. Eur J Haematol 2006;77(3):226–32.CrossRefGoogle Scholar
Shortt, J, Spencer, A. Adjuvant rituximab causes prolonged hypogammaglobulinaemia following autologous stem cell transplant for non-Hodgkin's lymphoma. Bone Marrow Transplant 2006;38(6):433–6.CrossRefGoogle ScholarPubMed
Miles, SA, McGratten, M. Persistent panhypogammaglobulinemia after CHOP-rituximab for HIV-related lymphoma. J Clin Oncol 2005;23(1):247–8.CrossRefGoogle ScholarPubMed
Chaiwatanatorn, K, Lee, N, Grigg, A, et al. Delayed-onset neutropenia associated with rituximab therapy. Br J Haematol 2003;121(6):913–18.CrossRefGoogle ScholarPubMed
Cairoli, R, Grillo, G, Tedeschi, A, et al. High incidence of neutropenia in patients treated with rituximab after autologous stem cell transplantation. Haematologica 2004;89(3):361–3.Google ScholarPubMed
Cattaneo, C, Spedini, P, Casari, S, et al. Delayed-onset peripheral blood cytopenia after rituximab: frequency and risk factor assessment in a consecutive series of 77 treatments. Leuk Lymphoma 2006;47(6):1013–17.CrossRefGoogle Scholar
Borg, C, Ray-Coquard, I, Philip, I, et al. CD4 lymphopenia as a risk factor for febrile neutropenia and early death after cytotoxic chemotherapy in adult patients with cancer. Cancer 2004;101(11):2675–80.CrossRefGoogle ScholarPubMed
Spina, M, Tirelli, U, Zagonel, V, et al. Burkitt's lymphoma in adults with and without human immunodeficiency virus infection: a single-institution clinicopathologic study of 75 patients. Cancer 1998;82(4):766–74.3.0.CO;2-V>CrossRefGoogle ScholarPubMed
Cortes, J, Thomas, D, Rios, A, et al. Hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone and highly active antiretroviral therapy for patients with acquired immunodeficiency syndrome-related Burkitt lymphoma/leukemia. Cancer 2002;94(5):1492–9.CrossRefGoogle ScholarPubMed
Oriol, A, Ribera, JM, Esteve, J, et al. Lack of influence of human immunodeficiency virus infection status in the response to therapy and survival of adult patients with mature B-cell lymphoma or leukemia. Results of the PETHEMA-LAL3/97 study. Haematologica 2003;88(4):445–53.Google ScholarPubMed
Wang, ES, Straus, DJ, Teruya-Feldstein, J, et al. Intensive chemotherapy with cyclophosphamide, doxorubicin, high-dose methotrexate/ifosfamide, etoposide, and high-dose cytarabine (CODOX-M/IVAC) for human immunodeficiency virus-associated Burkitt lymphoma. Cancer 2003;98(6):1196–205.CrossRefGoogle ScholarPubMed
Hoffmann, C, Wolf, E, Wyen, C, et al. AIDS-associated Burkitt or Burkitt-like lymphoma: short intensive polychemotherapy is feasible and effective. Leuk Lymphoma 2006;47(9):1872–80.CrossRefGoogle ScholarPubMed
Carbone, A. AIDS-related non-Hodgkin's lymphomas: from pathology and molecular pathogenesis to treatment. Hum Pathol 2002;33(4):392–404.CrossRefGoogle Scholar
Astrow, AB, Tarabay, G, Salerno, VE, et al. Long-term survival in patients with human immunodeficiency virus-associated small non-cleaved cell lymphoma: the role for short course intensive chemotherapy. Hematol Oncol 2003;21(3):131–40.CrossRefGoogle ScholarPubMed
Galicier, L, Fieschi, C, Borie, R, et al. Intensive chemotherapy regimen (LMB86) for St Jude stage IV AIDS-related Burkitt lymphoma/leukemia: a prospective study. Blood 2007;110(8):2846–54.CrossRefGoogle ScholarPubMed
Nicol, I, Boye, T, Carsuzaa, F, et al. Post-transplant plasmablastic lymphoma of the skin. Br J Dermatol 2003;149(4):889–91.CrossRefGoogle Scholar
Borenstein, J, Pezzella, F, Gatter, KC. Plasmablastic lymphomas may occur as post-transplant lymphoproliferative disorders. Histopathology 2007;51(6):774–7.CrossRefGoogle ScholarPubMed
Robak, T, Urbanska-Rys, H, Strzelecka, B, et al. Plasmablastic lymphoma in a patient with chronic lymphocytic leukemia heavily pretreated with cladribine (2-CdA): an unusual variant of Richter's syndrome. Eur J Haematol 2001;67(5–6):322–7.CrossRefGoogle Scholar
Redmond, M, Quinn, J, Murphy, P, et al. Plasmablastic lymphoma presenting as a paravertebral mass in a patient with Crohn's disease after immunosuppressive therapy. J Clin Pathol 2007;60(1):80–1.CrossRefGoogle Scholar
Sharma, R, Abdou, S, Plymyer, MR, et al. Disseminated plasmablastic lymphoma. J Am Coll Surg 2004;199(4):654–5.CrossRefGoogle ScholarPubMed
Hausermann, P, Khanna, N, Buess, M, et al. Cutaneous plasmablastic lymphoma in an HIV-positive male: an unrecognized cutaneous manifestation. Dermatology 2004;208(3):287–90.CrossRefGoogle Scholar
Jambusaria, A, Shafer, D, Wu, H, et al. Cutaneous plasmablastic lymphoma. J Am Acad Dermatol 2008;58(4):676–8.CrossRefGoogle ScholarPubMed
Delecluse, HJ, Anagnostopoulos, I, Dallenbach, F, et al. Plasmablastic lymphomas of the oral cavity: a new entity associated with the human immunodeficiency virus infection. Blood 1997;89(4):1413–20.Google ScholarPubMed
Carbone, A, Gaidano, G, Gloghini, A, et al. BCL-6 protein expression in AIDS-related non-Hodgkin's lymphomas: inverse relationship with Epstein-Barr virus-encoded latent membrane protein-1 expression. Am J Pathol 1997;150(1):155–65.Google ScholarPubMed
Flaitz, CM, Nichols, CM, Walling, DM, et al. Plasmablastic lymphoma: an HIV-associated entity with primary oral manifestations. Oral Oncol 2002;38(1):96–102.CrossRefGoogle ScholarPubMed
Teruya-Feldstein, J, Chiao, E, Filippa, DA, et al. CD20-negative large-cell lymphoma with plasmablastic features: a clinically heterogenous spectrum in both HIV-positive and -negative patients. Ann Oncol 2004;15(11):1673–9.CrossRefGoogle ScholarPubMed
Folk, GS, Abbondanzo, SL, Childers, EL, et al. Plasmablastic lymphoma: a clinicopathologic correlation. Ann Diagn Pathol 2006;10(1):8–12.CrossRefGoogle ScholarPubMed
Zanetto, U, Martin, CA, Sapia, S, et al. Re: Cioc, AM, Allen, C, Kalmar, J, et al. Oral plasmablastic lymphomas in AIDS patients are associated with human herpesvirus 8. Am J Surg Pathol 2004;25:41–46. Am J Surg Pathol 2004;28(11):1537–8; author reply 1538.Google Scholar
Nasta, SD, Carrum, GM, Shahab, I, et al. Regression of a plasmablastic lymphoma in a patient with HIV on highly active antiretroviral therapy. Leuk Lymphoma 2002;43(2):423–6.CrossRefGoogle Scholar
Lester, R, Li, C, Phillips, P, et al. Improved outcome of human immunodeficiency virus-associated plasmablastic lymphoma of the oral cavity in the era of highly active antiretroviral therapy: a report of two cases. Leuk Lymphoma 2004;45(9):1881–5.CrossRefGoogle ScholarPubMed
Nuovo, GJ.: Cioc, AM, Allen, C, Kalmar, J, et al. Oral plasmablastic lymphomas in AIDS patients are associated with human herpesvirus 8. Am J Surg Pathol 2004;25:41–46. Am J Surg Pathol 2004;28(9):1252–3.Google Scholar
Knowles, DM, Inghirami, G, Ubriaco, A, et al. Molecular genetic analysis of three AIDS-associated neoplasms of uncertain lineage demonstrates their B-cell derivation and the possible pathogenetic role of the Epstein-Barr virus. Blood 1989;73(3):792–9.Google ScholarPubMed
Green, I, Espiritu, E, Ladanyi, M, et al. Primary lymphomatous effusions in AIDS: a morphological, immunophenotypic, and molecular study. Mod Pathol 1995;8(1):39–45.Google ScholarPubMed
Walts, AE, Shintaku, IP, Said, JW. Diagnosis of malignant lymphoma in effusions from patients with AIDS by gene rearrangement. Am J Clin Pathol 1990;94(2):170–5.CrossRefGoogle ScholarPubMed
Carbone, A, Tirelli, U, Gloghini, A, et al. Herpesvirus-like DNA sequences selectively cluster with body cavity-based lymphomas throughout the spectrum of AIDS-related lymphomatous effusions. Eur J Cancer 1996;32A(3):555–6.CrossRefGoogle ScholarPubMed
Chadburn, A, Hyjek, E, Mathew, S, et al. KSHV-positive solid lymphomas represent an extra-cavitary variant of primary effusion lymphoma. Am J Surg Pathol 2004;28(11):1401–16.CrossRefGoogle ScholarPubMed
Komanduri, KV, Luce, JA, McGrath, MS, et al. The natural history and molecular heterogeneity of HIV-associated primary malignant lymphomatous effusions. J Acquir Immune Defic Syndr Hum Retrovirol 1996;13(3):215–26.CrossRefGoogle ScholarPubMed
Simonelli, C, Spina, M, Cinelli, R, et al. Clinical features and outcome of primary effusion lymphoma in HIV-infected patients: a single-institution study. J Clin Oncol 2003;21(21):3948–54.CrossRefGoogle ScholarPubMed
Boulanger, E, Gerard, L, Gabarre, J, et al. Prognostic factors and outcome of human herpesvirus 8-associated primary effusion lymphoma in patients with AIDS. J Clin Oncol 2005;23(19):4372–80.CrossRefGoogle ScholarPubMed
Ansari, MQ, Dawson, DB, Nador, R, et al. Primary body cavity-based AIDS-related lymphomas. Am J Clin Pathol 1996;105(2):221–9.CrossRefGoogle ScholarPubMed
Nador, RG, Cesarman, E, Chadburn, A, et al. Primary effusion lymphoma: a distinct clinicopathologic entity associated with the Kaposi's sarcoma-associated herpes virus. Blood 1996;88(2):645–56.Google ScholarPubMed
Brimo, F, Michel, RP, Khetani, K, et al. Primary effusion lymphoma: a series of 4 cases and review of the literature with emphasis on cytomorphologic and immunocytochemical differential diagnosis. Cancer 2007;111(4):224–33.CrossRefGoogle ScholarPubMed
Klein, U, Gloghini, A, Gaidano, G, et al. Gene expression profile analysis of AIDS-related primary effusion lymphoma (PEL) suggests a plasmablastic derivation and identifies PEL-specific transcripts. Blood 2003;101(10):4115–21.CrossRefGoogle ScholarPubMed
Fan, W, Bubman, D, Chadburn, A, et al. Distinct subsets of primary effusion lymphoma can be identified based on their cellular gene expression profile and viral association. J Virol 2005;79(2):1244–51.CrossRefGoogle ScholarPubMed
Chang, Y, Cesarman, E, Pessin, MS, et al. Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma. Science 1994;266(5192):1865–9.CrossRefGoogle ScholarPubMed
Cesarman, E, Chang, Y, Moore, PS, et al. Kaposi's sarcoma-associated herpesvirus-like DNA sequences in AIDS-related body-cavity-based lymphomas. N Engl J Med 1995;332(18):1186–91.CrossRefGoogle ScholarPubMed
Casper, C, Krantz, EM, Corey, L, et al. Valganciclovir for suppression of human herpesvirus-8 replication: a randomized, double-blind, placebo-controlled, crossover trial. J Infect Dis 2008;198(1):23–30.CrossRefGoogle ScholarPubMed
Simonelli, C, Tedeschi, R, Gloghini, A, et al. Characterization of immunologic and virological parameters in HIV-infected patients with primary effusion lymphoma during antiblastic therapy and highly active antiretroviral therapy. Clin Infect Dis 2005;40(7):1022–7.CrossRefGoogle ScholarPubMed
Keller, SA, Hernandez-Hopkins, D, Vider, J, et al. NF-κB is essential for the progression of KSHV- and EBV-infected lymphomas in vivo. Blood 2006;107(8):3295–302.CrossRefGoogle ScholarPubMed
Cote, TR, Manns, A, Hardy, CR, et al. Epidemiology of brain lymphoma among people with or without acquired immunodeficiency syndrome. AIDS/Cancer Study Group. J Natl Cancer Inst 1996;88(10):675–9.CrossRefGoogle ScholarPubMed
,International Collaboration on HIV and Cancer. Highly active antiretroviral therapy and incidence of cancer in human immunodeficiency virus-infected adults. J Natl Cancer Inst 2000;92(22):1823–30.CrossRefGoogle Scholar
Kadan-Lottick, NS, Skluzacek, MC, Gurney, JG. Decreasing incidence rates of primary central nervous system lymphoma. Cancer 2002;95(1):193–202.CrossRefGoogle ScholarPubMed
Bower, M, Powles, T, Nelson, M, et al. Highly active antiretroviral therapy and human immunodeficiency virus-associated primary cerebral lymphoma. J Natl Cancer Inst 2006;98(15):1088–91.CrossRefGoogle ScholarPubMed
Gray, F, Gherardi, R, Scaravilli, F.The neuropathology of the acquired immune deficiency syndrome (AIDS). A review. Brain 1988;111(Pt 2):245–66.CrossRefGoogle ScholarPubMed
Newell, ME, Hoy, JF, Cooper, SG, et al. Human immunodeficiency virus-related primary central nervous system lymphoma: factors influencing survival in 111 patients. Cancer 2004;100(12):2627–36.CrossRefGoogle ScholarPubMed
Raez, , Patel, P, Feun, L, et al. Natural history and prognostic factors for survival in patients with acquired immune deficiency syndrome (AIDS)-related primary central nervous system lymphoma (PCNSL). Crit Rev Oncog 1998;9(3–4):199–208.Google Scholar
Kasamon, YL, Ambinder, RF. AIDS-related primary central nervous system lymphoma. Hematol Oncol Clin North Am 2005;19(4):665–87, vi–vii.CrossRefGoogle ScholarPubMed
Cinque, P, Brytting, M, Vago, L, et al. Epstein-Barr virus DNA in cerebrospinal fluid from patients with AIDS-related primary lymphoma of the central nervous system. Lancet 1993;342(8868):398–401.CrossRefGoogle ScholarPubMed
Thurnher, MM, Thurnher, SA, Schindler, E. CNS involvement in AIDS: spectrum of CT and MR findings. Eur Radiol 1997;7(7):1091–7.CrossRefGoogle ScholarPubMed
Antinori, A, Rossi, G, Ammassari, A, et al. Value of combined approach with thallium-201 single-photon emission computed tomography and Epstein-Barr virus DNA polymerase chain reaction in CSF for the diagnosis of AIDS-related primary CNS lymphoma. J Clin Oncol 1999;17(2):554–60.CrossRefGoogle Scholar
Hoffman, JM, Waskin, HA, Schifter, T, et al. FDG-PET in differentiating lymphoma from nonmalignant central nervous system lesions in patients with AIDS. J Nucl Med 1993;34(4):567–75.Google ScholarPubMed
Pierce, MA, Johnson, MD, Maciunas, RJ, et al. Evaluating contrast-enhancing brain lesions in patients with AIDS by using positron emission tomography. Ann Intern Med 1995;123(8):594–8.CrossRefGoogle ScholarPubMed
Heald, AE, Hoffman, JM, Bartlett, JA, et al. Differentiation of central nervous system lesions in AIDS patients using positron emission tomography (PET). Int J STD AIDS 1996;7(5):337–46.CrossRefGoogle Scholar
Roelcke, U, Leenders, KL. Positron emission tomography in patients with primary CNS lymphomas. J Neurooncol 1999;43(3):231–6.CrossRefGoogle ScholarPubMed
Cingolani, A, Luca, A, Larocca, LM, et al. Minimally invasive diagnosis of acquired immunodeficiency syndrome-related primary central nervous system lymphoma. J Natl Cancer Inst 1998;90(5):364–9.CrossRefGoogle ScholarPubMed
Corcoran, C, Rebe, K, Plas, H, et al. The predictive value of cerebrospinal fluid Epstein-Barr viral load as a marker of primary central nervous system lymphoma in HIV-infected persons. J Clin Virol 2008;42(4):433–6.CrossRefGoogle ScholarPubMed
Bossolasco, S, Falk, KI, Ponzoni, M, et al. Ganciclovir is associated with low or undetectable Epstein-Barr virus DNA load in cerebrospinal fluid of patients with HIV-related primary central nervous system lymphoma. Clin Infect Dis 2006;42(4):e21–5.CrossRefGoogle ScholarPubMed
Skiest, DJ, Crosby, C. Survival is prolonged by highly active antiretroviral therapy in AIDS patients with primary central nervous system lymphoma. AIDS 2003;17(12):1787–93.CrossRefGoogle ScholarPubMed
Chamberlain, MC, Kormanik, PA. AIDS-related central nervous system lymphomas. J Neurooncol 1999;43(3):269–76.CrossRefGoogle ScholarPubMed
Ferreri, AJ, Reni, M, Pasini, F, et al. A multicenter study of treatment of primary CNS lymphoma. Neurology 2002;58(10):1513–20.CrossRefGoogle ScholarPubMed
Ferreri, AJ, Reni, M, Villa, E. Therapeutic management of primary central nervous system lymphoma: lessons from prospective trials. Ann Oncol 2000;11(8):927–37.CrossRefGoogle ScholarPubMed
Batchelor, T, Carson, K, O'Neill, A, et al. Treatment of primary CNS lymphoma with methotrexate and deferred radiotherapy: a report of NABTT 96-07. J Clin Oncol 2003;21(6):1044–9.CrossRefGoogle ScholarPubMed
Jacomet, C, Girard, PM, Lebrette, MG, et al. Intravenous methotrexate for primary central nervous system non-Hodgkin's lymphoma in AIDS. AIDS 1997;11(14):1725–30.CrossRefGoogle Scholar
Sarker, D, Thirlwell, C, Nelson, M, et al. Leptomeningeal disease in AIDS-related non-Hodgkin's lymphoma. AIDS 2003;17(6):861–5.CrossRefGoogle ScholarPubMed
Hill, QA, Owen, RG. CNS prophylaxis in lymphoma: who to target and what therapy to use. Blood Rev 2006;20(6):319–32.CrossRefGoogle ScholarPubMed
Navarro, JT, Vall-Llovera, F, Mate, JL, et al. Decrease in the frequency of meningeal involvement in AIDS-related systemic lymphoma in patients receiving HAART. Haematologica 2008;93(1):149–50.CrossRefGoogle ScholarPubMed
Cingolani, A, Gastaldi, R, Fassone, L, et al. Epstein-Barr virus infection is predictive of CNS involvement in systemic AIDS-related non-Hodgkin's lymphomas. J Clin Oncol 2000;18(19):3325–30.CrossRefGoogle ScholarPubMed
Desai, J, Mitnick, RJ, Henry, DH, et al. Patterns of central nervous system recurrence in patients with systemic human immunodeficiency virus-associated non-hodgkin lymphoma. Cancer 1999;86(9):1840–7.3.0.CO;2-C>CrossRefGoogle ScholarPubMed
Hegde, U, Filie, A, Little, RF, et al. High incidence of occult leptomeningeal disease detected by flow cytometry in newly diagnosed aggressive B-cell lymphomas at risk for central nervous system involvement: the role of flow cytometry versus cytology. Blood 2005;105(2):496–502.CrossRefGoogle ScholarPubMed
Di Noto, R, Scalia, G, Abate, G, et al. Critical role of multidimensional flow cytometry in detecting occult leptomeningeal disease in newly diagnosed aggressive B-cell lymphomas. Leuk Res 2008;32(8):1196–9.CrossRefGoogle ScholarPubMed
Gold, JE, Altarac, D, Ree, HJ, et al. HIV-associated Hodgkin disease: a clinical study of 18 cases and review of the literature. Am J Hematol 1991;36(2):93–9.CrossRefGoogle ScholarPubMed
Errante, D, Zagonel, V, Vaccher, E, et al. Hodgkin's disease in patients with HIV infection and in the general population: comparison of clinicopathological features and survival. Ann Oncol 1994;5 (Suppl 2):37–40.CrossRefGoogle Scholar
Andrieu, JM, Roithmann, S, Tourani, JM, et al. Hodgkin's disease during HIV1 infection: the French registry experience. French Registry of HIV-associated Tumors. Ann Oncol 1993;4(8):635–41.CrossRefGoogle ScholarPubMed
Tirelli, U, Errante, D, Dolcetti, R, et al. Hodgkin's disease and human immunodeficiency virus infection: clinicopathologic and virologic features of 114 patients from the Italian Cooperative Group on AIDS and Tumors. J Clin Oncol 1995;13(7):1758–67.CrossRefGoogle ScholarPubMed
Thompson, LD, Fisher, SI, Chu, WS, et al. HIV-associated Hodgkin lymphoma: a clinicopathologic and immunophenotypic study of 45 cases. Am J Clin Pathol 2004;121(5):727–38.CrossRefGoogle ScholarPubMed
Dawson, MA, Schwarer, AP, McLean, C, et al. AIDS-related plasmablastic lymphoma of the oral cavity associated with an IGH/MYC translocation–treatment with autologous stem-cell transplantation in a patient with severe haemophilia-A. Haematologica 2007;92(1):e11–12.CrossRefGoogle Scholar
Bosch Princep, R, Lejeune, M, Salvado Usach, MT, et al. Decreased number of granzyme B+ activated CD8+ cytotoxic T lymphocytes in the inflammatory background of HIV-associated Hodgkin's lymphoma. Ann Hematol 2005;84(10):661–6.CrossRefGoogle ScholarPubMed
Errante, D, Tirelli, U, Gastaldi, R, et al. Combined antineoplastic and antiretroviral therapy for patients with Hodgkin's disease and human immunodeficiency virus infection. A prospective study of 17 patients. The Italian Cooperative Group on AIDS and Tumors (GICAT). Cancer 1994;73(2):437–44.3.0.CO;2-2>CrossRefGoogle Scholar
Errante, D, Gabarre, J, Ridolfo, AL, et al. Hodgkin's disease in 35 patients with HIV infection: an experience with epirubicin, bleomycin, vinblastine and prednisone chemotherapy in combination with antiretroviral therapy and primary use of G-CSF. Ann Oncol 1999;10(2):189–95.CrossRefGoogle ScholarPubMed
Levine, AM, Li, P, Cheung, T, et al. Chemotherapy consisting of doxorubicin, bleomycin, vinblastine, and dacarbazine with granulocyte-colony-stimulating factor in HIV-infected patients with newly diagnosed Hodgkin's disease: a prospective, multi-institutional AIDS clinical trials group study (ACTG 149). J Acquir Immune Defic Syndr 2000;24(5):444–50.CrossRefGoogle Scholar
Gastaldi, R, Martino, P, Gentile, G, et al. Hodgkin's disease in HIV-infected patients: report of eight cases usefully treated with doxorubicin, bleomycin, vinblastine and dacarbazine (ABVD) plus granulocyte colony-stimulating factor. Ann Oncol 2002;13(7):1158–60.CrossRefGoogle ScholarPubMed
Xicoy, B, Ribera, JM, Miralles, P, et al. Results of treatment with doxorubicin, bleomycin, vinblastine and dacarbazine and highly active antiretroviral therapy in advanced stage, human immunodeficiency virus-related Hodgkin's lymphoma. Haematologica 2007;92(2):191–8.CrossRefGoogle ScholarPubMed
Hartmann, P, Rehwald, U, Salzberger, B, et al. BEACOPP therapeutic regimen for patients with Hodgkin's disease and HIV infection. Ann Oncol 2003;14(10):1562–9.CrossRefGoogle ScholarPubMed
Marti-Carvajal, AJ, Cardona, AF, Rodriguez, ML. Interventions for treating AIDS-associated Hodgkin's lymphoma in treatment-naive adults. Cochrane Database Syst Rev 2007;Issue 2: CD006149. DOI: 10.1002/14651858.CD006149.pub2.CrossRef
Collins, JA, Hernandez, AV, Hidalgo, JA, et al. High proportion of T-cell systemic non-Hodgkin lymphoma in HIV-infected patients in Lima, Peru. J Acquired Immune Defic Syndr 2005;40(5):558–64.CrossRefGoogle ScholarPubMed
Chadburn, A, Cesarman, E, Jagirdar, J, et al. CD30 (Ki-1) positive anaplastic large cell lymphomas in individuals infected with the human immunodeficiency virus. Cancer 1993;72(10):3078–90.3.0.CO;2-F>CrossRefGoogle ScholarPubMed
Nosari, A, Cantoni, S, Oreste, P, et al. Anaplastic large cell (CD30/Ki-1+) lymphoma in HIV+ patients: clinical and pathological findings in a group of ten patients. Br J Haematol 1996;95(3):508–12.CrossRefGoogle Scholar
Arzoo, KK, Bu, X, Espina, BM, et al. T-cell lymphoma in HIV-infected patients. J Acquir Immune Defic Syndr 2004;36(5):1020–7.CrossRefGoogle ScholarPubMed
Ruco, LP, Di Napoli, A, Pilozzi, E, et al. Peripheral T cell lymphoma with cytotoxic phenotype: an emerging disease in HIV-infected patients?AIDS Res Hum Retroviruses 2004;20(2):129–33.CrossRefGoogle ScholarPubMed
Carbone, A, Gloghini, A, Volpe, R, et al. High frequency of Epstein-Barr virus latent membrane protein-1 expression in acquired immunodeficiency syndrome-related Ki-1 (CD30)-positive anaplastic large-cell lymphomas. Italian Cooperative Group on AIDS and Tumors. Am J Clin Pathol 1994;101(6):768–72.CrossRefGoogle ScholarPubMed
Oksenhendler, E, Duarte, M, Soulier, J, et al. Multicentric Castleman's disease in HIV infection: a clinical and pathological study of 20 patients. AIDS 1996;10(1):61–7.CrossRefGoogle ScholarPubMed
Oksenhendler, E, Boulanger, E, Galicier, L, et al. High incidence of Kaposi sarcoma-associated herpesvirus-related non-Hodgkin lymphoma in patients with HIV infection and multicentric Castleman disease. Blood 2002;99(7):2331–6.CrossRefGoogle ScholarPubMed
Oksenhendler, E, Carcelain, G, Aoki, Y, et al. High levels of human herpesvirus 8 viral load, human interleukin-6, interleukin-10, and C reactive protein correlate with exacerbation of multicentric Castleman disease in HIV-infected patients. Blood 2000;96(6):2069–73.Google Scholar
Aoki, Y, Yarchoan, R, Wyvill, K, et al. Detection of viral interleukin-6 in Kaposi sarcoma-associated herpesvirus-linked disorders. Blood 2001;97(7): 2173–6.CrossRefGoogle ScholarPubMed
Aoki, Y, Tosato, G, Fonville, TW, et al. Serum viral interleukin-6 in AIDS-related multicentric Castleman disease. Blood 2001;97(8):2526–7.CrossRefGoogle ScholarPubMed
Baloon, G, Cesarman, E.Castleman's Disease. Hamilton, ON, BC Decker, 2006.Google Scholar
Navarro, WH, Kaplan, LD. AIDS-related lymphoproliferative disease. Blood 2006;107(1):13–20.CrossRefGoogle ScholarPubMed
Casper, C. The aetiology and management of Castleman disease at 50 years: translating pathophysiology to patient care. Br J Haematol 2005;129(1):3–17.CrossRefGoogle ScholarPubMed
Carbone, A, Cesarman, E, Spina, M, et al. HIV-associated lymphomas and gamma-herpesviruses. Blood 2009;113(6):1213–24.CrossRefGoogle ScholarPubMed
Dupin, N, Diss, TL, Kellam, P, et al. HHV-8 is associated with a plasmablastic variant of Castleman disease that is linked to HHV-8-positive plasmablastic lymphoma. Blood 2000;95(4):1406–12.Google ScholarPubMed
Amin, HM, Medeiros, LJ, Manning, JT, et al. Dissolution of the lymphoid follicle is a feature of the HHV8+ variant of plasma cell Castleman's disease. Am J Surg Pathol 2003;27(1):91–100.CrossRefGoogle ScholarPubMed
Du, MQ, Liu, H, Diss, TC, et al. Kaposi sarcoma-associated herpesvirus infects monotypic (IgM lambda) but polyclonal naive B cells in Castleman disease and associated lymphoproliferative disorders. Blood 2001;97(7):2130–6.CrossRefGoogle ScholarPubMed
Lanzafame, M, Carretta, G, Trevenzoli, M, et al. Successful treatment of Castleman's disease with HAART in two HIV-infected patients. J Infect 2000;40(1):90–1.CrossRefGoogle ScholarPubMed
Marcelin, AG, Aaron, L, Mateus, C, et al. Rituximab therapy for HIV-associated Castleman disease. Blood 2003;102(8):2786–8.CrossRefGoogle ScholarPubMed
Bower, M, Powles, T, Williams, S, et al. Brief communication: rituximab in HIV-associated multicentric Castleman disease. Ann Intern Med 2007;147(12):836–9.CrossRefGoogle ScholarPubMed
Gerard, L, Berezne, A, Galicier, L, et al. Prospective study of rituximab in chemotherapy-dependent human immunodeficiency virus associated multicentric Castleman's disease: ANRS 117 CastlemaB Trial. J Clin Oncol 2007;25(22):3350–6.CrossRefGoogle ScholarPubMed
Fragasso, A, Mannarella, C, Ciancio, A, et al. Complete remission and virologic response to combined chemoimmunotherapy (R-CVP) followed by rituximab maintenance in HIV-negative, HHV-8 positive patient with multicentric Castleman disease. Leuk Lymphoma 2008;49(11):2224–6.CrossRefGoogle ScholarPubMed
Bestawros, A, Michel, R, Seguin, C, et al. Multicentric Castleman's disease treated with combination chemotherapy and rituximab in four HIV-positive men: a case series. Am J Hematol 2008;83(6):508–11.CrossRefGoogle ScholarPubMed
Stary, G, Kohrgruber, N, Herneth, AM, et al. Complete regression of HIV-associated multicentric Castleman disease treated with rituximab and thalidomide. AIDS 2008;22(10):1232–4.CrossRefGoogle ScholarPubMed
Casper, C, Nichols, WG, Huang, ML, et al. Remission of HHV-8 and HIV-associated multicentric Castleman disease with ganciclovir treatment. Blood 2004;103(5):1632–4.CrossRefGoogle ScholarPubMed
Berezne, A, Agbalika, F, Oksenhendler, E. Failure of cidofovir in HIV-associated multicentric Castleman disease. Blood 2004;103(11):4368–9; author reply 4369.CrossRefGoogle ScholarPubMed
Coty, PC, Astrow, AB, Gallinson, D. Splenectomy is an effective treatment for HIV-associated multicentric Castleman's disease. Blood 2003;102:Abstract 3899.Google Scholar
Philip, T, Guglielmi, C, Hagenbeek, A, et al. Autologous bone marrow transplantation as compared with salvage chemotherapy in relapses of chemotherapy-sensitive non-Hodgkin's lymphoma. N Engl J Med 1995;333(23):1540–5.CrossRefGoogle ScholarPubMed
Nademanee, A, Molina, A, Dagis, A, et al. Autologous stem-cell transplantation for poor-risk and relapsed intermediate- and high-grade non-Hodgkin's lymphoma. Clin Lymphoma 2000;1(1):46–54.CrossRefGoogle ScholarPubMed
Re, A, Cattaneo, C, Michieli, M, et al. High-dose therapy and autologous peripheral-blood stem-cell transplantation as salvage treatment for HIV-associated lymphoma in patients receiving highly active antiretroviral therapy. J Clin Oncol 2003;21(23):4423–7.CrossRefGoogle ScholarPubMed
Gabarre, J, Marcelin, AG, Azar, N, et al. High-dose therapy plus autologous hematopoietic stem cell transplantation for human immunodeficiency virus (HIV)-related lymphoma: results and impact on HIV disease. Haematologica 2004;89(9):1100–8.Google ScholarPubMed
Krishnan, A, Molina, A, Zaia, J, et al. Durable remissions with autologous stem cell transplantation for high-risk HIV-associated lymphomas. Blood 2005;105(2):874–8.CrossRefGoogle ScholarPubMed
Serrano, D, Carrion, R, Balsalobre, P, et al. HIV-associated lymphoma successfully treated with peripheral blood stem cell transplantation. Exp Hematol 2005;33(4):487–94.CrossRefGoogle ScholarPubMed
Balsalobre, BN, Serrano, D, Re, A, et al. Autologous stem cell transplantation (ASCT) in HIV associated lymphoma (HIV-Ly) patients: The EBMT Lymphoma Working Party (EBMT-LWP) experience. Blood 2006;108:Abstract 3042.Google Scholar
Spitzer, TR, Ambinder, RF, Lee, JY, et al. Dose-reduced busulfan, cyclophosphamide, and autologous stem cell transplantation for human immunodeficiency virus-associated lymphoma: AIDS Malignancy Consortium study 020. Biol Blood Marrow Transplant 2008;14(1):59–66.CrossRefGoogle ScholarPubMed
Wagner-Johnston, ND, Ambinder, RF. Blood and marrow transplant for lymphoma patients with HIV/AIDS. Curr Opin Oncol 2008;20(2):201–5.CrossRefGoogle ScholarPubMed
Bi, J, Espina, BM, Tulpule, A, et al. High-dose cytosine-arabinoside and cisplatin regimens as salvage therapy for refractory or relapsed AIDS-related non-Hodgkin's lymphoma. J Acquir Immune Defic Syndr 2001;28(5):416–21.CrossRefGoogle ScholarPubMed

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