Impact of ovarian transposition before pelvic irradiation on ovarian function among long‐term survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort Study
Background We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy. Procedure Female participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically eval...
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Published in: | Pediatric blood & cancer Vol. 65; no. 9; pp. e27232 - n/a |
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Abstract | Background
We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy.
Procedure
Female participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically evaluated for premature ovarian insufficiency (POI) 10 or more years after pelvic radiotherapy. Reproductive history including age at menopause and pregnancy/live births was available on all patients.
Results
Of 127 eligible females with HL, 90 (80%) participated in SJLIFE, including 49 who underwent OT before pelvic radiotherapy. Median age at STLIFE evaluation was 38 years (range 25–60). In a multiple regression adjusted for age at diagnosis, pelvic radiotherapy doses > 1,500 cGy (hazard ratio [HR] = 25.2, 95% confidence interval [CI] = 3.1–207.3; P = 0.0027) and cumulative cyclophosphamide equivalent doses of alkylating agents > 12,000 mg/m2 (HR = 11.2, 95% CI = 3.4–36.8; P < 0.0001) were significantly associated with POI. There was no significant association between OT and occurrence of POI (HR = 0.6, 95% CI = 0.2–1.9; P = 0.41).
Conclusions
OT did not appear to modify risk of POI in this historic cohort of long‐term survivors of HL treated with gonadotoxic therapy. Modern fertility preservation modalities, such as mature oocyte cryopreservation, should be offered to at‐risk patients whenever feasible. |
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AbstractList | Abstract
Background
We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy.
Procedure
Female participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically evaluated for premature ovarian insufficiency (POI) 10 or more years after pelvic radiotherapy. Reproductive history including age at menopause and pregnancy/live births was available on all patients.
Results
Of 127 eligible females with HL, 90 (80%) participated in SJLIFE, including 49 who underwent OT before pelvic radiotherapy. Median age at STLIFE evaluation was 38 years (range 25–60). In a multiple regression adjusted for age at diagnosis, pelvic radiotherapy doses > 1,500 cGy (hazard ratio [HR] = 25.2, 95% confidence interval [CI] = 3.1–207.3;
P
= 0.0027) and cumulative cyclophosphamide equivalent doses of alkylating agents > 12,000 mg/m
2
(HR = 11.2, 95% CI = 3.4–36.8;
P
< 0.0001) were significantly associated with POI. There was no significant association between OT and occurrence of POI (HR = 0.6, 95% CI = 0.2–1.9;
P
= 0.41).
Conclusions
OT did not appear to modify risk of POI in this historic cohort of long‐term survivors of HL treated with gonadotoxic therapy. Modern fertility preservation modalities, such as mature oocyte cryopreservation, should be offered to at‐risk patients whenever feasible. We reviewed the effect of ovarian transposition (OT) on ovarian function among long-term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy. Female participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically evaluated for premature ovarian insufficiency (POI) 10 or more years after pelvic radiotherapy. Reproductive history including age at menopause and pregnancy/live births was available on all patients. Of 127 eligible females with HL, 90 (80%) participated in SJLIFE, including 49 who underwent OT before pelvic radiotherapy. Median age at STLIFE evaluation was 38 years (range 25-60). In a multiple regression adjusted for age at diagnosis, pelvic radiotherapy doses > 1,500 cGy (hazard ratio [HR] = 25.2, 95% confidence interval [CI] = 3.1-207.3; P = 0.0027) and cumulative cyclophosphamide equivalent doses of alkylating agents > 12,000 mg/m (HR = 11.2, 95% CI = 3.4-36.8; P < 0.0001) were significantly associated with POI. There was no significant association between OT and occurrence of POI (HR = 0.6, 95% CI = 0.2-1.9; P = 0.41). OT did not appear to modify risk of POI in this historic cohort of long-term survivors of HL treated with gonadotoxic therapy. Modern fertility preservation modalities, such as mature oocyte cryopreservation, should be offered to at-risk patients whenever feasible. BackgroundWe reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy.ProcedureFemale participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically evaluated for premature ovarian insufficiency (POI) 10 or more years after pelvic radiotherapy. Reproductive history including age at menopause and pregnancy/live births was available on all patients.ResultsOf 127 eligible females with HL, 90 (80%) participated in SJLIFE, including 49 who underwent OT before pelvic radiotherapy. Median age at STLIFE evaluation was 38 years (range 25–60). In a multiple regression adjusted for age at diagnosis, pelvic radiotherapy doses > 1,500 cGy (hazard ratio [HR] = 25.2, 95% confidence interval [CI] = 3.1–207.3; P = 0.0027) and cumulative cyclophosphamide equivalent doses of alkylating agents > 12,000 mg/m2 (HR = 11.2, 95% CI = 3.4–36.8; P < 0.0001) were significantly associated with POI. There was no significant association between OT and occurrence of POI (HR = 0.6, 95% CI = 0.2–1.9; P = 0.41).ConclusionsOT did not appear to modify risk of POI in this historic cohort of long‐term survivors of HL treated with gonadotoxic therapy. Modern fertility preservation modalities, such as mature oocyte cryopreservation, should be offered to at‐risk patients whenever feasible. Background We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic radiotherapy. Procedure Female participants (age 18+ years) with HL in the St. Jude Lifetime Cohort Study (SJLIFE) were clinically evaluated for premature ovarian insufficiency (POI) 10 or more years after pelvic radiotherapy. Reproductive history including age at menopause and pregnancy/live births was available on all patients. Results Of 127 eligible females with HL, 90 (80%) participated in SJLIFE, including 49 who underwent OT before pelvic radiotherapy. Median age at STLIFE evaluation was 38 years (range 25–60). In a multiple regression adjusted for age at diagnosis, pelvic radiotherapy doses > 1,500 cGy (hazard ratio [HR] = 25.2, 95% confidence interval [CI] = 3.1–207.3; P = 0.0027) and cumulative cyclophosphamide equivalent doses of alkylating agents > 12,000 mg/m2 (HR = 11.2, 95% CI = 3.4–36.8; P < 0.0001) were significantly associated with POI. There was no significant association between OT and occurrence of POI (HR = 0.6, 95% CI = 0.2–1.9; P = 0.41). Conclusions OT did not appear to modify risk of POI in this historic cohort of long‐term survivors of HL treated with gonadotoxic therapy. Modern fertility preservation modalities, such as mature oocyte cryopreservation, should be offered to at‐risk patients whenever feasible. |
Author | Fernandez‐Pineda, Israel Robison, Leslie L. Green, Daniel M. Davidoff, Andrew M. Srivastava, D. Kumar Sklar, Charles A. Krasin, Matthew J. Hudson, Melissa M. Ness, Kirsten K. Rao, Bhaskar N. Pui, Ching‐Hon Chemaitilly, Wassim Wilson, Carmen L. Lu, Lu Klosky, James L. Metzger, Monica L. |
AuthorAffiliation | 3 Department of Biostatistics, St Jude Children’s Research Hospital, Memphis, TN (USA) 1 Department of Surgery, St Jude Children’s Research Hospital, Memphis, TN (USA) 5 Department of Oncology, St Jude Children’s Research Hospital, Memphis, TN (USA) 8 Department of Pediatric Medicine, Division of Endocrinology, St Jude Children’s Research Hospital, Memphis, TN (USA) 7 Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY (USA) 4 Department of Psychology, St Jude Children’s Research Hospital, Memphis, TN (USA) 6 Department of Radiation Oncology, St Jude Children’s Research Hospital, Memphis, TN (USA) 2 Department of Epidemiology and Cancer Control, St Jude Children’s Research Hospital, Memphis, TN (USA) |
AuthorAffiliation_xml | – name: 1 Department of Surgery, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 4 Department of Psychology, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 2 Department of Epidemiology and Cancer Control, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 3 Department of Biostatistics, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 7 Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY (USA) – name: 5 Department of Oncology, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 8 Department of Pediatric Medicine, Division of Endocrinology, St Jude Children’s Research Hospital, Memphis, TN (USA) – name: 6 Department of Radiation Oncology, St Jude Children’s Research Hospital, Memphis, TN (USA) |
Author_xml | – sequence: 1 givenname: Israel orcidid: 0000-0001-5605-695X surname: Fernandez‐Pineda fullname: Fernandez‐Pineda, Israel email: israel.fernandez-pineda@stjude.org organization: St. Jude Children's Research Hospital – sequence: 2 givenname: Andrew M. surname: Davidoff fullname: Davidoff, Andrew M. organization: St. Jude Children's Research Hospital – sequence: 3 givenname: Lu surname: Lu fullname: Lu, Lu organization: St. Jude Children's Research Hospital – sequence: 4 givenname: Bhaskar N. surname: Rao fullname: Rao, Bhaskar N. organization: St. Jude Children's Research Hospital – sequence: 5 givenname: Carmen L. orcidid: 0000-0001-7636-065X surname: Wilson fullname: Wilson, Carmen L. organization: St. Jude Children's Research Hospital – sequence: 6 givenname: D. Kumar surname: Srivastava fullname: Srivastava, D. Kumar organization: St. Jude Children's Research Hospital – sequence: 7 givenname: James L. surname: Klosky fullname: Klosky, James L. organization: St. Jude Children's Research Hospital – sequence: 8 givenname: Monica L. surname: Metzger fullname: Metzger, Monica L. organization: St. Jude Children's Research Hospital – sequence: 9 givenname: Matthew J. surname: Krasin fullname: Krasin, Matthew J. organization: St. Jude Children's Research Hospital – sequence: 10 givenname: Kirsten K. surname: Ness fullname: Ness, Kirsten K. organization: St. Jude Children's Research Hospital – sequence: 11 givenname: Ching‐Hon orcidid: 0000-0003-0303-5658 surname: Pui fullname: Pui, Ching‐Hon organization: St. Jude Children's Research Hospital – sequence: 12 givenname: Leslie L. surname: Robison fullname: Robison, Leslie L. organization: St. Jude Children's Research Hospital – sequence: 13 givenname: Melissa M. surname: Hudson fullname: Hudson, Melissa M. organization: St. Jude Children's Research Hospital – sequence: 14 givenname: Charles A. surname: Sklar fullname: Sklar, Charles A. organization: Memorial Sloan Kettering Cancer Center – sequence: 15 givenname: Daniel M. surname: Green fullname: Green, Daniel M. organization: St. Jude Children's Research Hospital – sequence: 16 givenname: Wassim surname: Chemaitilly fullname: Chemaitilly, Wassim organization: St. Jude Children's Research Hospital |
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Cites_doi | 10.1002/pbc.24348 10.1210/jc.2006-2374 10.1016/S0022-3476(05)80332-4 10.1148/96.1.175 10.1038/bjc.1976.29 10.1016/j.fertnstert.2008.09.029 10.1001/archsurg.1970.01340210012004 10.1002/(SICI)1096-911X(199905)32:5<366::AID-MPO10>3.0.CO;2-7 10.1056/NEJM198106043042301 10.1016/j.fertnstert.2012.09.028 10.1097/01.AOG.0000451757.51964.98 10.1259/0007-1285-62-743-995 10.1210/jc.2006-0020 10.1210/jc.2016-3723 10.1002/pbc.22875 10.1002/pbc.24679 10.1002/(SICI)1097-0142(19991115)86:10<2138::AID-CNCR36>3.0.CO;2-V 10.1093/jnci/djj243 10.1016/S0015-0282(16)49268-X 10.1097/00001648-199911000-00022 10.1002/1097-0142(197612)38:6<2263::AID-CNCR2820380612>3.0.CO;2-S 10.1016/0002-9378(58)90614-8 |
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Keywords | ovarian transposition premature ovarian insufficiency late effects Hodgkin lymphoma |
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Notes | This study was presented as an oral presentation at the annual meeting of the International Society of Paediatric Oncology (SIOP), Washington DC, in October 2017. Grant sponsor: National Cancer Institute (NIH), Grant number: CA 21765, Grant sponsor: ALSAC ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with... We reviewed the effect of ovarian transposition (OT) on ovarian function among long-term survivors of childhood Hodgkin lymphoma (HL) treated with pelvic... Abstract Background We reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL)... BackgroundWe reviewed the effect of ovarian transposition (OT) on ovarian function among long‐term survivors of childhood Hodgkin lymphoma (HL) treated with... BACKGROUNDWe reviewed the effect of ovarian transposition (OT) on ovarian function among long-term survivors of childhood Hodgkin lymphoma (HL) treated with... |
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SubjectTerms | Age Alkylating agents Alkylation Children Cohort analysis Cryopreservation Cyclophosphamide Females Fertility Health risk assessment Hematology Hodgkin lymphoma Hodgkin's lymphoma Irradiation late effects Lymphoma Menopause Oncology ovarian transposition Pediatrics Pregnancy premature ovarian insufficiency Radiation therapy Reproductive status Transposition |
Title | Impact of ovarian transposition before pelvic irradiation on ovarian function among long‐term survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort Study |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpbc.27232 https://www.ncbi.nlm.nih.gov/pubmed/29750388 https://www.proquest.com/docview/2073803386 https://search.proquest.com/docview/2038270630 https://pubmed.ncbi.nlm.nih.gov/PMC6105417 |
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