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32 - Late reproductive sequelae of treatment for childhood cancer

from Part III - Management of specific disorders

Published online by Cambridge University Press:  04 May 2010

Angela B. Thomson
Affiliation:
Department of Haematology/Oncology, Royal Hospital for Sick Children, Edinburgh, UK
Hilary O.D. Critchley
Affiliation:
Department of Developmental and Reproductive Sciences, University of Edinburgh, Edinburgh, UK
Christopher J. H. Kelnar
Affiliation:
Department of Developmental and Reproductive Sciences, University of Edinburgh, Edinburgh, UK
W. Hamish B. Wallace
Affiliation:
Department of Haematology/Oncology, Royal Hospital for Sick Children, Edinburgh, UK
Adam H. Balen
Affiliation:
Leeds Teaching Hospitals, University Trust
Sarah M. Creighton
Affiliation:
University College London Hospitals
Melanie C. Davies
Affiliation:
University College London
Jane MacDougall
Affiliation:
Addenbrooke's Hospital, Cambridge
Richard Stanhope
Affiliation:
Great Ormond Street Hospital
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Summary

Introduction

Tremendous therapeutic advances in the management of childhood malignancies mean that the majority of children can realistically hope for long-term survival. Cancer in childhood is rare, with about 1400 new cases per year in the UK and a cumulative risk of 1 in 650 by the age of 15 years (Stiller, 1997; Wallace, 1997). With survival rates in excess of 70%, it is estimated that by the year 2010, 1 in 250 of the young adult population will be a long-term survivor of childhood cancer (Fig. 32.1) (Bleyer, 1990). However, the successful treatment of cancer in childhood with chemotherapy and or radiotherapy is associated with a number of unwanted side effects in later life (Wallace et al., 2001). Therefore, the major challenge faced by paediatric oncologists today is to sustain the excellent survival rates while striving to improve the quality of life of the survivors.

One of the most important issues for the survivors of childhood cancer is the impact of their disease and its treatment on reproductive function and the implications for the health of their offspring. In the female, chemotherapy and radiotherapy may damage the ovary and hasten oocyte depletion, resulting in loss of hormone production, truncated fecundity and a premature menopause (Meirow, 2000; Thomson et al., 2002). Infertility is one of the most commonly encountered and psychologically traumatic late complications of treatment for childhood cancer, and consequently, strategies to preserve fertile potential are being pursued.

Type
Chapter
Information
Paediatric and Adolescent Gynaecology
A Multidisciplinary Approach
, pp. 397 - 415
Publisher: Cambridge University Press
Print publication year: 2004

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References

Abir, R, Franks, S, Mobberley, M A, Moore, P A, Margara, R A, Winston, R M (1997). Mechanical isolation and in vitro growth of preantral and small antral human follicles. Fertil Steril 68, 682–688CrossRefGoogle ScholarPubMed
Abir, R, Fisch, B, Raz, A, Nitke, S, Ben-Rafael, Z (1998). Preservation of fertility in women undergoing chemotherapy: current approach and future prospects. J Assist Reprod Genet 15, 469–478CrossRefGoogle ScholarPubMed
Ahmed Eddiary, N A, Lenton, E A, Cooke, I D (1994). Hypothalamic—pituitary ageing: progressive increase in FSH and LH concentrations throughout the reproductive life in regularly menstruating women. Clin Endocrinol 41, 199–206Google Scholar
Ataya, K, Ramahi-Ataya, A (1993). Reproductive performance of female rats treated with cyclophosphamide and/or LHRH agonist. Reprod Toxicol 7, 229–235CrossRefGoogle ScholarPubMed
Ataya, K, Rao, L V, Lawrence, E, Kimmel, R (1995a). Luteinizing hormone-releasing hormone agonist inhibits cyclophosphamide-induced ovarian follicle depletion in rhesus monkeys. Biol Reprod 52, 365–372CrossRefGoogle Scholar
Ataya, K, Pydyn, E, Ramahi-Ataya, A, Orton, C G (1995b). Is radiation-induced ovarian failure in rhesus monkeys preventable by leuteinizing hormone-releasing hormone agonist? Preliminary observations. J Clin Oncol Endocrinol Metab 80, 790–795Google Scholar
Atkinson, H G, Apperley, J F, Dawson, K, Goldman, J M, Winston, R M (1994). Successful pregnancy after embryo cryopreservation after BMT for CML. Lancet 344, 199CrossRefGoogle Scholar
Baird, D T, Webb, R, Campbell, B K, Harkness, L M, Gosden, R G (1999). Long-term ovarian function in sheep after ovariectomy and transplantation of autografts stored at —196℃C. Endocrinology 140, 462–471CrossRefGoogle Scholar
Balow, J E (1993). Risk for sustained amenorrhoea in patients with systemic lupus erythematosus receiving intermittent pulse cyclophosphamide therapy. Ann Intern Med 1, 366–369Google Scholar
Bath, L E, Critchley, H O, Chambers, S E, Anderson, R A, Kelnar, C J, Wallace, W H (1999). Ovarian and uterine characteristics after total body irradiation in childhood and adolescence: response to sex steroid replacement. Br J Obstet Gynaecol 106, 1265–1272CrossRefGoogle ScholarPubMed
Bath, L E, Anderson, R A, Critchley, H O D, Kelnar, C J H, Wallace, W H B (2001). Hypothalamic—pituitary—ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia. Hum Reprod 16, 1838–1844CrossRefGoogle ScholarPubMed
Bines, J, Oleske, D M, Cobleigh, M A (1996). Ovarian function in premenopausal women treated with adjuvant chemotherapy for breast cancer. J Clin Oncol 14, 1718–1729CrossRefGoogle ScholarPubMed
Birkebaek, N H, Fisker, S, Clausen, N, Tuovinen, V, Sindet-Pedersen, S, Christiansen, J S (1998). Growth and endocrinological disorders up to 21 years after treatment for acute lymphoblastic leukaemia in childhood. Med Pediatr Oncol 30, 351–3563.0.CO;2-D>CrossRefGoogle ScholarPubMed
Bleyer, W A (1990). The impact of childhood cancer on the United States and the world. Cancer 40, 355–367Google Scholar
Block, E (1952). Quantitative morphological investigations of the follicular system in women. Variations at different ages. Acta Anat 14, 108–123CrossRefGoogle ScholarPubMed
Block, E (1953). A quantitative morphological investigation of the follicular system in newborn female infants. Acta Anat 17, 201–206CrossRefGoogle ScholarPubMed
Blumenfeld, Z (2000). Ovarian rescue/protection from chemotherapeutic agents (1). J Soc Gynecol Invest 8, S60–S64Google Scholar
Blumenfeld, Z, Avivi, I, Linn, S, Epelbaum, R, Ben-Shahar, M, Haim, N (1996). Prevention of irreversible chemotherapy-induced ovarian damage in young women with lymphoma by a gonadotrophin-releasing hormone agonist in parallel to chemotherapy. Hum Reprod 11, 1620–1626CrossRefGoogle Scholar
Blumenfeld, Z, Shapiro, D, Shteinberg, M, Avivi, I, Nahir, M (2000). Preservation of fertility and ovarian function and minimizing gonadotoxicity in young women with systemic lupus erythematosus treated by chemotherapy. Lupus 9, 401–405CrossRefGoogle ScholarPubMed
Bosma, G C, Custer, R P, Bosma, M J (1983). A severe combined deficiency mutation in the mouse. Nature 301, 527–530CrossRefGoogle ScholarPubMed
Boumpas, D T, Austin, H A III, Vaughan, E M, Yarboro, C H, Klippel, J H, Balow J E (1993). Risk for sustained amenorrhoea in patients with systemic lupus erythematosus receiving intermittent pulse cyclophosphamide therapy. Ann Intern Med 1, 366–369CrossRefGoogle Scholar
Brennan, B M, Rahim, A, Mackie, E M, Eden, O B, Shalet, S M (1998). Growth hormone status in adults treated for acute lymphoblastic leukaemia in childhood. Clin Endocrinol 48, 777–783CrossRefGoogle ScholarPubMed
Brook, P F, Radford, J A, Shalet, S M, Joyce, A D, Gosden, R G (2001). Isolation of germ cells from human testicular tissue for low temperature storage and autotransplantation. Fertil Steril 75, 269–274CrossRefGoogle ScholarPubMed
Brusamolino, E, Lunghi, F, Orlandi, E et al. (2000). Treatment of early-stage Hodgkin's disease with four cycles of ABVD followed by adjuvant radiotherapy:analysis and efficacy and long-term toxicity. Haematologica 85, 103–105Google ScholarPubMed
Byrne, J, Fears, T R, Gail, M H et al. (1992). Early menopause in long-term survivors of cancer during adolescence. Am J Obstet Gynecol 166, 788–793CrossRefGoogle ScholarPubMed
Cain, L, Chatterjee, S, Collins, T J (1995). In vitro folliculogenesis of rat preantral follicles. Endocrinology 136, 3369–3377CrossRefGoogle ScholarPubMed
Candy, C J, Wood, M J, Whittingham, D G (1995). Follicular development in cryopreserved marmoset ovarian tissue after transplantation. Hum Reprod 10, 2334–2338CrossRefGoogle ScholarPubMed
Candy, C J, Wood, M J, Whittingham, D G (2000). Restoration of normal reproductive life span after grafting of cryopreserved ovaries. Hum Reprod 15, 1300–1304CrossRefGoogle Scholar
Carroll, J, Gosden, R G (1993). Transplantation of frozen-thawed mouse primordial follicles. Hum Reprod 8, 1163–1167CrossRefGoogle ScholarPubMed
Chatterjee, R, Goldstone, A H (1996). Gonadal damage and effects on fertility in adult patients with haematological malignancy undergoing stem cell transplantation. Bone Marrow Transplant 17, 159–167Google ScholarPubMed
Chapman, A M, Marrett, L D, Darlington, G (1979). Cytotoxic-induced ovarian failure in Hodgkin's disease. I. Hormone function. J Am Med Assoc 242, 1877–1881CrossRefGoogle ScholarPubMed
Chapman, R M, Sutcliffe, S B, Malpas, J S (1981). Cytotoxic-induced ovarian failure in women treated with MOPP chemotherapy for Hodgkin's disease. Am J Med 71, 552–556Google Scholar
Chiarelli, A M, Marrett, L D, Darlington, G (1999). Early menopause and infertility in females after treatment for childhood cancer diagnosed in 1964–1988 in Ontario, Canada. Am J Epidemiol 150, 245–254CrossRefGoogle ScholarPubMed
Clark, S T, Radford, J A, Crowther, D, Swindell, R, Shalet, S M (1995). Cytotoxic induced ovarian failure in women treated for Hodgkin's disease: a comparative study of MVPP and a seven-drug hybrid regimen. J Clin Oncol 13, 134–139CrossRefGoogle Scholar
Cox, S L, Shaw, J M, Jenkin, G (1996). Transplantation of cryopreserved fetal ovarian tissue to adult recipients in mice. J Reprod Fertil 107, 315–322CrossRefGoogle ScholarPubMed
Critchley, H O, Buckley, C H, Anderson, D C (1990). Experience with a ‘physiological’ steroid replacement regimen for the establishment of a receptive endometrium in women with premature ovarian failure. Br J Obstet Gynaecol 97, 804–810CrossRefGoogle ScholarPubMed
Critchley, H O, Wallace, W H, Shalet, S M, Mamtora, H, Higginson, J, Anderson, D C (1992). Abdominal irradiation in childhood; the potential for pregnancy. Br J Obstet Gynaecol 99, 392–394CrossRefGoogle ScholarPubMed
Critchley, H O, Wang, H, Kelly, R W, Gebbie, A E, Glasier, A F (1998). Progestin receptor isoforms and prostaglandin dehydrogenase in the endometrium of women using a levonorgestrel-releasing intrauterine system. Hum Reprod 13, 1210–1217CrossRefGoogle ScholarPubMed
Crowne, E C, Moore, C, Wallace, W H B et al. (1992). A novel variant of growth hormone insufficiency following low dose cranial irradiation. Clin Endocrinol 36, 59–68CrossRefGoogle ScholarPubMed
Eppig, J J, O'Brien, M (1996). Development in vitro of mouse oocytes from primordial follicles. Biol Reprod 54, 197–207CrossRefGoogle ScholarPubMed
Eppig, D G, Schroeder, A C (1989). Capacity of mouse oocytes from preantral follicles to undergo embryogenesis and development to live young after growth, maturation, and fertilization in vitro. Biol Reprod 41, 268–276CrossRefGoogle ScholarPubMed
Faddy, M J, Gosden, R G (1996). A model conforming the decline in follicle numbers to the age of menopause in women. Hum Reprod 11, 1484–1486CrossRefGoogle ScholarPubMed
Faddy, M J, Gosden, R G, Edwards, R (1983). Ovarian follicle dynamics in mice: a comparative study of three inbred strains and an F1 hybrid. J Endocrinol 96, 23–33CrossRefGoogle ScholarPubMed
Faddy, M J, Gosden, R G, Gougeon, A, Richardson, S J, Nelson, J F (1992). Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Hum Reprod 7, 1342–1346CrossRefGoogle ScholarPubMed
Familiari, G, Caggiati, A, Nottola, S A, Ermini, M, Di Benedetto, M R, Motta, P M (1993). Ultrastructure of human ovarian primordial follicles after combination chemotherapy for Hodgkin's disease. Hum Reprod 8, 2080–2087CrossRefGoogle ScholarPubMed
Fisher, B, Cheung, A Y (1984). Delayed effect of radiation therapy with or without chemotherapy on ovarian function in women with Hodgkin's disease. Acta Radiol Oncol 23, 43–48CrossRefGoogle ScholarPubMed
Gosden, R G (1990). Restitution of fertility in sterilised mice by transferring primordial ovarian follicles. Hum Reprod 5, 117–122CrossRefGoogle Scholar
Gosden, R G, Baird, D T, Wade, J C, Webb, R (1994a). Restoration of fertility to oopherectomized sheep by ovarian autografts stored at -196℃C. Hum Reprod 9, 597–603CrossRefGoogle Scholar
Gosden, R G, Boulton, M I, Grant, K, Webb, R (1994b). Follicular development from ovarian xenografts in SCID mice. J Reprod Fertil 101, 619–623CrossRefGoogle Scholar
Gosden, R G, Wade, J C, Fraser, H M, Sandow, J, Faddy, M J (1997a). Impact of congenital and experimental hypogonadism on the radiation sensitivity of the mouse ovary. Hum Reprod 12, 2483–2488CrossRefGoogle Scholar
Gosden, R G, Rutherford, A J, Norfolk, D R (1997b). Ovarian banking for cancer patients: transmission of malignant cells in ovarian grafts. Hum Reprod 12, 403Google Scholar
Green, D M, Hall, B, Zevon, A (1989). Pregnancy outcome after treatment for acute lymphoblastic leukaemia during childhood or adolescence. Cancer 64, 235–2443.0.CO;2-7>CrossRefGoogle ScholarPubMed
Green, S H, Smith, A U, Zuckerman, S (1956). The number of oocytes in ovarian autografts after freezing and thawing. J Endocrinol 13, 333–334CrossRefGoogle ScholarPubMed
Greenwald, G S, Moor, R M (1989). Isolation and preliminary characterization of pig primordial follicles. J Reprod Fertil 87, 561–571CrossRefGoogle ScholarPubMed
Grundy, R, Gosden, R G, Hewitt, M et al. (2001a). Fertility preservation for children treated for cancer (1): scientific advances and research dilemmas. Arch Dis Child 84, 355–359CrossRefGoogle Scholar
Grundy, R, Larcher, V, Gosden, R G et al. (2001b). Personal practice: fertility preservation for children treated for cancer (2); ethics of consent for gamete storage and experimentation. Arch Dis Child 84, 360–362CrossRefGoogle Scholar
Guanasena, K T, Villines, P M, Crister, E S, Crister, J K (1997). Live births with autologous transplant of cryopreserved mouse ovaries. Hum Reprod 12, 101–116CrossRefGoogle Scholar
Hawkins, M M (1994). Pregnancy outcome and offspring after childhood cancer. Br Med J 309, 1034–1040CrossRefGoogle ScholarPubMed
Hawkins, M M, Smith, R A (1989). Pregnancy outcomes in childhood cancer survivors; probable effect of abdominal irradiation. Int J Cancer 43, 399–402CrossRefGoogle Scholar
Hawkins, M M, Draper, G J, Smith, R A (1989). Cancer among 1348 survivors of childhood cancer. Int J Cancer 43, 975–978CrossRefGoogle ScholarPubMed
Holm, K, Laursen, E M, Brocks, V, Muller, J (1995). Pubertal maturation of the internal genitalia: an ultrasound evaluation of 166 healthy girls. Ultrasound Obstet Gynecol 6, 155–181CrossRefGoogle ScholarPubMed
Hovatta, O, Silye, R, Kraustz, T et al. (1996). Cryopreservation of human ovarian tissue by using dimethylsulphoxide and propandiol-sucrose as cryoprotectants. Hum Reprod 11, 1268–1272CrossRefGoogle ScholarPubMed
Hudson, M M, Greenwald, C, Thompson, E et al. (1993). Efficacy and toxicity of multi agent chemotherapy and low-dose involved-field radiotherapy in children and adolescents with Hodgkin's disease. J Clin Oncol 11, 100–108CrossRefGoogle Scholar
Kim, S S, Gosden, R G, Radford, J A et al. (1999). A model to test the safety of human ovarian tissue transplantation after cryopreservation: xenografts of ovarian tissue from cancer patients into NOD/LtSz-scid mice. [Annual Meeting of the American Society of Reproductive Medicine, Toronto, Canada.] Fertil Steril Suppl p. 3Google Scholar
Larsen, E C, Loft, A, Holm, K, Muller, J, Brocks, V, Anderson, A N (2000). Oocyte donation in women cured of cancer with bone marrow transplantation including total body irradiation in adolescence. Hum Reprod 15, 1505–1508CrossRefGoogle ScholarPubMed
Leporrier, M, Theobald, P, Roffe, J L, Muller, G (1987). A new technique to protect ovarian function in young women undergoing pelvic irradiation. Heterotopic ovarian autotransplantation. Cancer 60, 2201–22043.0.CO;2-Z>CrossRefGoogle Scholar
Li, F P, Fine, W, Jaffe, N, Holmes, G E, Holmes, F F (1979). Offspring of patients treated for cancer in childhood. J Natl Cancer Inst 62, 1193–1197Google ScholarPubMed
Li, F P, Gimbrere, K, Gelber, R D et al. (1987). Outcome of pregnancy in survival of Wilm's tumour. J Am Med Assoc 257, 216–219CrossRefGoogle Scholar
Littley, M D, Shalet, S M, Beardwell, C G, Ahmed, S R, Applegate, G, Sutton, M L (1989). Hypopituitarism following external radiotherapy for pituitary tumours in adults. Q J Med 70, 145–160Google ScholarPubMed
Livesey, E A, Brook, C G D (1988). Gonadal dysfunction after treatment of intracranial tumours. Arch Dis Child 63, 495–500CrossRefGoogle ScholarPubMed
Louis, L, Lemaryi, L R, Best, W R (1956). Treatment of chronic granulocytic leukaemia with myleran. Arch Int Med 97, 299–308CrossRefGoogle ScholarPubMed
Ludwig, M, Al-Hasani, S, Felderbaum, R, Diedrich, K (1999). New aspects of cryopreservation of oocytes and embryos in assisted reproduction and future perspectives. Hum Reprod 14, 162–185CrossRefGoogle ScholarPubMed
Lushbaugh, C C, Casarett, G W (1976). The effects of gonadal irradiation in clinical radiation therapy: a review. Cancer 37, 1111–11253.0.CO;2-E>CrossRefGoogle ScholarPubMed
Mackie, E J, Radford, M, Shalet, S M (1996). Gonadal function following chemotherapy for childhood Hodgkin's disease. Med Pediatr Oncol 27, 74–783.0.CO;2-Q>CrossRefGoogle ScholarPubMed
Matsumoto, M, Shinohara, O, Ishiguro, H et al. (1999). Ovarian function after bone marrow transplantation performed before menarche. Arch Dis Child 80, 452–454CrossRefGoogle ScholarPubMed
Marcello, M F, Nuciforo, G, Romeo, R et al. (1990). Structural and ultrastructural study of the ovary in childhood leukaemia after successful treatment. Cancer 66, 2099–21043.0.CO;2-3>CrossRefGoogle ScholarPubMed
Meirow, D (1999).Ovarian injury and modern options to preserve fertility in female cancer patients treated with high-dose radio-chemotherapy for haemato-oncological neoplasias and other cancers. Leuk Lymphoma 33, 65–76CrossRefGoogle Scholar
Meirow, D (2000). Reproduction post chemotherapy in young cancer patients. Mol Cell Endocrinol 169, 123–131CrossRefGoogle ScholarPubMed
Meirow, D, Nugent, D, Epstein, M et al. (1998). An in vitro study of the effects of chemotherapy on human primordial follicles. Hum ReprodA13Google Scholar
Mok, C C, Lau, C S, Wong, R W (1998). Risk factors for ovarian failure in patients with systemic lupus erythematosus receiving cyclophosphamide therapy. Arthritis Rheum 41, 831–837Google ScholarPubMed
Montz, F J, Wolff, A J, Gambone, J C (1991). Gonadal protection and fecundity rates in cyclophosphamide-treated rats. Cancer Res 51, 2124–2126Google ScholarPubMed
Moore, H C (2000). Following treatment for breast cancer. The incidence of treatment related amenorrhoea is related to patient age and to the treatment regimen. Curr Oncol Rep 2, 587–593CrossRefGoogle Scholar
Morita, Y, Perez, G I, Paris, F et al. (2000). Oocyte apoptosis is suppressed by disruption of the acid sphingomyelinase gene or by sphingosine-1-phosphate therapy. Nat Med 6, 1109–1114CrossRefGoogle ScholarPubMed
Nicholson, H S, Byrne, J (1993). Fertility and pregnancy after treatment for cancer during childhood or adolescence. Cancer 71, 3392–33993.0.CO;2-F>CrossRefGoogle ScholarPubMed
Nugent, D, Meirow, D, Brook, P F, Aubard Y, Gosden R G (1997). Transplantation in reproductive medicine: previous experience, present knowledge and future prospects. Hum Reprod Update 3, 267–280CrossRefGoogle ScholarPubMed
Nygaard, R, Clausen, N, Simes, M A et al. (1991). Reproduction following treatment for childhood leukaemia: a population based prospective cohort study of fertility and offspring. Med Pediatr Oncol 19, 459–466CrossRefGoogle ScholarPubMed
Oktay, K (2001). Ovarian tissue cryopreservation and transplantation: preliminary findings and implications for cancer patients. Hum Reprod Update 7, 526–534CrossRefGoogle ScholarPubMed
Oktay, K, Karlikaya, G (2000). Ovarian function after transplantation of frozen, banked, autologous ovarian tissue. N Engl J Med 342, 1919CrossRefGoogle ScholarPubMed
Oktay, K, Nugent, D, Newton, H, Salha, O, Chatterjee, P, Gosden, R G (1997). Isolation and characterization of primordial follicles from fresh and cryopreserved human ovarian tissue. Fertil Steril 67, 481–486CrossRefGoogle ScholarPubMed
Oktay, K, Newton, H, Mullan, J, Gosden, R G (1998). Development of human primordial follicles to antral stages in SCID/hpg mice stimulated with follicle stimulating hormone. Hum Reprod 13, 1133–1138CrossRefGoogle ScholarPubMed
Oktay, K, Karlikaya, G G, Aydin, B A (2000a). Ovarian cryopreservation and transplantation: basic aspects. Mol Cell Endocrinol 169, 105–108CrossRefGoogle Scholar
Oktay, K, Newton, H, Gosden, R G (2000b). Transplantation of cryopreserved human ovarian tissue results in follicle growth initiation in SCID mice. Fertil Steril 73, 599–603CrossRefGoogle Scholar
Oktay, K, Economos, K, Kan, M, Rucinski, J, Veeck, L, Rosenwaks, Z (2001). Endocrine function and oocyte retrieval after autologous transplantation of ovarian cortical strips to the forearm. J Am Med Assoc 286, 1490–1493CrossRefGoogle ScholarPubMed
Parkes, A S, Smith, A U (1952). Regeneration of rat ovarian tissue grafted after exposure to low temperatures. Proc Roy Soc Lond 140, 455–467CrossRefGoogle Scholar
Parrot, D M (1960). The fertility of mice with orthotopic grafts derived from frozen tissue. J Reprod Fertil 1, 230–241CrossRefGoogle Scholar
Pasqualini, T, Escobar, M E, Domene, H, Muriel, F S, Pavlovsky, S, Rivarola, M A (1987). Evaluation of gonadal function following long-term treatment for acute lymphoblastic leukaemia in girls. Am J Pediatr Hematol Oncol 9, 15–22CrossRefGoogle ScholarPubMed
Perez, G I, Knudson, C M, Leykin, L, Korsmeyer, S J, Tilly, J L (1997). Apoptosis-associated signalling pathways are required for chemotherapy-mediated female germ cell destruction. Nat Med 3, 1228–1232CrossRefGoogle Scholar
Perez, G I, Maravei, D V, Trbovich, A M, Cidlowski, J A, Tilly, J L, Hughes, F M Jr (2000). Identification of the potassium-dependent and -independent components of the apoptotic machinery in mouse ovarian germ cells and granulosa cells. Biol Reprod 63, 1358–1369CrossRefGoogle ScholarPubMed
Porcu, E, Fabbri, R, Seracchioli, R, Ciotti, P M, Magrini, O, Flamigni, C (1997). Birth of a healthy female after intracytoplasmic sperm injection of cryopreserved human oocytes. Fertil Steril 68, 724–726CrossRefGoogle ScholarPubMed
Radford, J A, Leibermann, B A, Brison, D R et al. (2001). Orthotopic reimplantation of cryopreserved ovarian cortical strips after high-dose chemotherapy for Hodgkin's lymphoma. Lancet 357, 1172–1175CrossRefGoogle ScholarPubMed
Richardson, S J, Senikas, V, Nelson, J F (1987). Follicular depletion during the menopausal transition: evidence for accelerated loss and ultimate exhaustion. J Clin Endocrinol Metab 65, 1231–1237CrossRefGoogle ScholarPubMed
Robertson, C M, Hawkins, M M, Kingston, J E (1994). Late deaths and survival after children with cancer: implications for cure. Br Med J 309, 162–166CrossRefGoogle ScholarPubMed
Roy, S K, Greenwald, G S (1989). Hormonal requirements for the growth and differentiation of hamster preantral follicles in long-term culture. J Reprod Fertil 87, 103–114CrossRefGoogle ScholarPubMed
Roy, S K, Treacy, B J (1993). Isolation and long-term culture of human preantral follicles. Fertil Steril 59, 783–790CrossRefGoogle ScholarPubMed
Royal College of Obstetricians and Gynaecologists (2000). Storage of Ovarian and Prepubertal Testicular Tissue: Report of a Working Party. Royal College of Obstetricians and Gynaecologists, London
Salooja, N, Szydlo, R M, Socie, G et al. (2001). Pregnancy outcomes after peripheral blood or bone marrow transplantation: a retrospective survey. Lancet 358, 271–276CrossRefGoogle ScholarPubMed
Sanders, J E (1991). The impact of marrow transplant preparation regimens on subsequent growth and development. Semin Hematol 28, 244–249Google ScholarPubMed
Sanders, J E, Hawley, J, Levy, W et al. (1996). Pregnancies following high-dose cyclophosphamide with or without high-dose busulfan or total-body irradiation and bone marrow transplantation. Blood 87, 3045–3052Google ScholarPubMed
Sanger, W G, Olson, J H, Sherman, J K (1992). Semen cryobanking for men with cancer: criteria change. Fertil Steril 58, 1024–1027CrossRefGoogle ScholarPubMed
Schimmer, A D, Quatermain, M, Imrie, K et al. (1998). Ovarian function after bone marrow transplantation. J Clin Oncol 16, 2359–2363CrossRefGoogle ScholarPubMed
Shaw, J M, Bowles, J, Koopman, P, Wood, E C, Trounson A O (1996). Fresh and cryopreserved ovarian tissue samples from donors with lymphoma transmit the cancer to graft recipients. Hum Reprod 11, 1668–1673CrossRefGoogle ScholarPubMed
Shaw, J M, Cox, S L, Trounson, A O, Jenkin, G (2000). Evaluation of the long-term function of cryopreserved ovarian grafts in the mouse, implications for human applications. Mol Cell Endocrinol 161, 103–110CrossRefGoogle ScholarPubMed
Sherman, B M, West, J H, Korenman, S G (1976). The menopausal transition: analysis of LH, FSH, estradiol, and progesterone concentrations during menstrual cycles of older women. J Clin Endocrinol Metab 42, 629–636CrossRefGoogle ScholarPubMed
Siris, E S, Leventhal, B G, Vaitukaitis, J L (1976). Effects of childhood leukaemia and chemotherapy on puberty and reproductive function in girls. N Engl J Med 294, 1143–1146CrossRefGoogle ScholarPubMed
Snijders, M P, Goeij, A F, Debets-Te, Baerts M J, Rousch, M J, Koudstaal, J, Bosman, F T (1992). Immunocytochemical analysis of oestrogen receptors and progesterone receptors in the human uterus throughout the menstrual cycle and after the menopause. J Reprod Fertil 94, 363–371CrossRefGoogle ScholarPubMed
Spears, N, Boland, N I, Murray, A A, Gosden, R G (1994). Mouse oocytes derived from in vitro grown primary ovarian follicles are fertile. Hum Reprod 9, 527–532CrossRefGoogle ScholarPubMed
Stiller C A (1997). Aetiology and epidemiology. In Paediatric Oncology: Clinical Practice and Controversies, 2nd edn, Pinkerton C R, Plowman P N, eds., pp. 3–21. Chapman & Hall, London
SyOrtin, T T, Shostak, C A, Donaldson, S S (1990). Gonadal status and reproductive function following treatment for Hodgkin's disease in childhood: the Stanford experience. Int J Radiat Oncol, Biol, Phys 304, 1377–1382Google Scholar
Sztein, J M, O'Brie, M J, Farley, J S, Mobraaten, L (1998). Cryopreservation and orthotopic transplantation of mouse ovaries: new approach in gamete banking. Biol Reprod 58, 1071–1074CrossRefGoogle ScholarPubMed
Teinturier, C, Hartmann, O, Valteau-Couanet, D, Benhamou, E, Bougneres, P F (1998). Ovarian function after autologous bone marrow transplantation in childhood: high dose busulfan is a major cause of ovarian failure. Bone Marrow Transplant 22, 989–994CrossRefGoogle ScholarPubMed
Thibaud, E, Rodriguez-Macias, K, Trivin, C, Esperou, H, Michon, J, Brauner, R (1998). Ovarian function after bone marrow transplantation. Bone Marrow Transplant 21, 287–290CrossRefGoogle ScholarPubMed
Thomas, P R, Winstanly, D, Peckham, M J, Austin, D E, Murray, M A, Jacobs, H S (1976). Reproductive and endocrine function in patients with Hodgkin's disease: effects of oopheropexy and irradiation. Br J Cancer 33, 226–231CrossRefGoogle Scholar
Thomson, A B, Critchley, H O D, Kelnar, C J H, Wallace, W H B (2002). Late reproductive sequelae following treatment of childhood cancer and options for fertility preservation. Adult sequelae of childhood endocrine disorders. Baillière's Best Pract Res Clin Endocrinol Metab 16, 311–334CrossRefGoogle Scholar
Torrance, C, Telfer, E, Gosden, R G (1989). Quantitative study of the development of isolated mouse pre-antral follicles in collagen gel culture. J Reprod Fertil 87, 367–374CrossRefGoogle ScholarPubMed
Wallace W H B (1997). Growth and endocrine function following the treatment of childhood malignant disease. In Paediatric Oncology: Clinical Practice and Controversies, 2nd edn, Pinkerton C R, Plowman P N, eds., pp. 706–731. Chapman & Hall, London
Wallace, W H B, Walker, D A (2001). Conference consensus statement: ethical and research dilemmas for fertility preservation in children treated for cancer. Hum Fertil 4, 69–76CrossRefGoogle ScholarPubMed
Wallace, W H, Shalet, S M, Crowne, E C, Morris-Jones, P H, Gattamaneni, H R (1989a). Ovarian failure following abdominal irradiation in childhood: natural history and prognosis. Clin Oncol 1, 75–79CrossRefGoogle Scholar
Wallace, W H, Shalet, S M, Hendry, J H, Morris-Jones, P H, Gattamaneni, H R (1989b). Ovarian failure following abdominal irradiation in childhood: The radiosensitivity of the human oocyte. Br J Radiol 62, 995–998CrossRefGoogle Scholar
Wallace, W H B, Shalet, S M, Crowne, E C, Morris-Jones, P H, Gattamaneni, H R, Price, D A (1989c). Gonadal dysfunction due to cis-platinum. Med Pediatr Oncol 17, 409–413CrossRefGoogle Scholar
Wallace, W H, Shalet, S M, Tetlow, L J, Morris-Jones, P H (1993). Ovarian function following the treatment of childhood acute lymphoblastic leukaemia. Med Pediatr Oncol 21, 333–339CrossRefGoogle ScholarPubMed
Wallace, W H B, Blacklay, A, Eiser, C et al. (2001). Developing strategies for long term follow up of survivors of childhood cancer. Br Med J 323, 271–274CrossRefGoogle ScholarPubMed
Wallace, W H B, Thomson, A B, Kelsey, T W (2003). The radiosensitivity of the human oocyte. Hum Reprod 18, 117–121CrossRefGoogle ScholarPubMed
Waxman, J H X, Terry, Y A, Wrigley, P F M et al. (1982). Gonadal function in Hodgkin's disease: long-term follow-up of chemotherapy. Br Med J 285, 1612–1613CrossRefGoogle ScholarPubMed
Weissman, A, Gotlieb, L, Colgan, T, Jurisicova, A, Greenblatt, E M, Casper, R F (1999). Preliminary experience with subcutaneous human ovarian cortex transplantation in the NOD-SCID mouse. Biol Reprod 60, 1462–1467CrossRefGoogle ScholarPubMed
Wells, S A Jr, Ellis, G J, Gunnells, J C, Schneider, A B, Sherwood, L M (1976). Parathyroid autotransplantation in parathyroid hyperplasia. N Engl J Med 295, 57–62CrossRefGoogle ScholarPubMed
Whitehead, E, Shalet, S M, Blackledge, G, Todd, I, Crowther, D, Beardwell, C G (1983). The effect of combination chemotherapy on ovarian function in women treated for Hodgkin's disease. Cancer 52, 988–9933.0.CO;2-6>CrossRefGoogle ScholarPubMed

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