Ovarian function in female survivors of high-risk neuroblastoma Journal Article


Authors: Jimenez-Kurlander, L.; DeRosa, A.; Kostrzewa, C. E.; Moskowitz, C. S.; Bogardus, K.; Antal, Z.; Wolden, S.; La Quaglia, M. P.; Basu, E. M.; Cardenas, F. I.; Kramer, K.; Kushner, B. H.; Cheung, N. K. V.; Modak, S.; Friedman, D. N.
Article Title: Ovarian function in female survivors of high-risk neuroblastoma
Abstract: Introduction: Data on ovarian function in neuroblastoma survivors are limited. We sought to determine the prevalence of ovarian dysfunction in a cohort of high-risk neuroblastoma survivors and compare outcomes among survivors treated with and without autologous stem cell rescue (ASCR) preceded by myeloablative chemotherapy. Methods: Retrospective review of female survivors of high-risk neuroblastoma ≥5 years from diagnosis, diagnosed between 1982 and 2014, and followed in a tertiary cancer center. Participants were divided into two groups: individuals treated with conventional chemotherapy ± radiation (“non-ASCR”) (n = 32) or with chemotherapy ± radiation followed by myeloablative chemotherapy with ASCR (“ASCR”) (n = 51). Ovarian dysfunction was defined as follicle-stimulating hormone ≥15 mU/mL, while premature ovarian insufficiency (POI) was defined as persistent ovarian dysfunction requiring hormone replacement therapy. Poisson models were used to determine prevalence ratios of ovarian dysfunction and POI. Results: Among 83 females (median attained age: 19 years [range, 10-36]; median follow-up: 15 years [range, 7-36]), 49 (59%) had ovarian dysfunction, and 34 (41%) developed POI. Survivors treated with ASCR were 3.2-fold more likely to develop ovarian dysfunction (95% CI: 1.8-6.0; p < 0.001) and 4.5-fold more likely to develop POI (95% CI: 1.7-11.7; p = 0.002) when compared with those treated with conventional chemotherapy, after adjusting for attained age. Two participants in the non-ASCR group and six in the ASCR group achieved at least one spontaneous pregnancy. Discussion: Ovarian dysfunction is prevalent in female high-risk neuroblastoma survivors, especially after ASCR. Longitudinal follow-up of larger cohorts is needed to inform counseling about the risk of impaired ovarian function after neuroblastoma therapy. © 2024 Wiley Periodicals LLC.
Keywords: neuroblastoma; childhood cancer survivors; fertility preservation; ovarian function; autologous hematopoietic stem cell rescue
Journal Title: Pediatric Blood and Cancer
Volume: 71
Issue: 9
ISSN: 1545-5009
Publisher: Wiley Periodicals, Inc  
Date Published: 2024-09-01
Start Page: e31181
Language: English
DOI: 10.1002/pbc.31181
PUBMED: 38967225
PROVIDER: scopus
PMCID: PMC11269001
DOI/URL:
Notes: The MSK Cancer Center Support Grant (P30 CA008748) is acknowledge in the PDF -- Source: Scopus
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MSK Authors
  1. Brian Kushner
    311 Kushner
  2. Nai-Kong Cheung
    648 Cheung
  3. Kim Kramer
    236 Kramer
  4. Shakeel Modak
    249 Modak
  5. Suzanne L Wolden
    560 Wolden
  6. Chaya S. Moskowitz
    278 Moskowitz
  7. Danielle Novetsky Friedman
    110 Friedman
  8. Ellen Marlese Basu
    101 Basu
  9. Amelia DeRosa
    4 DeRosa
  10. Zoltan Antal
    19 Antal