Loading…

Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations: Clinical Oncology/Epidemiology

Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionna...

Full description

Saved in:
Bibliographic Details
Published in:British journal of cancer 1996-07, Vol.74 (2), p.291-296
Main Authors: Swerdlow, AJ, Jacobs, PA, Marks, A, Maher, EJ, Young, T, Barber, JCK, Vaughan Hudson, G
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 296
container_issue 2
container_start_page 291
container_title British journal of cancer
container_volume 74
creator Swerdlow, AJ
Jacobs, PA
Marks, A
Maher, EJ
Young, T
Barber, JCK
Vaughan Hudson, G
description Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionnaires to the patients. Eleven men and 16 women who had conceived any children after treatment were then interviewed. There was no excess of stillbirths, low birthweight or cogenital malformations, and no cancers have occurred in the 49 offspring after treatment. There was a significant excess of twins, compared with national expectations, in offspring of female patients (RR = 8.52, P = 0.025). Aggregation of series from the literature also showed an excess of twins. Chromosomes from cultures of peripheral lymphocytes from 45 children born to 25 patients (11 men and 14 women) after treatment were examined for numerical abnormalities and for structural abnormalities at the 550 or greater band level of resolution. All were normal except in one child with Down's syndrome (47, XY, +21), for whom we found the origin of the trisomy was from the parent without Hodgkin's disease. The chromosome constitution was also abnormal in one miscarriage (69, XXY; originating from the parent without Hodgkin's disease) and one termination (45, X; for with the parental origin could not be determined) after treatment. The study adds to previous questionnaire data and for the first time provides data also from chromosome analysis, that offspring of patients treated in adulthood for Hodgkin's disease are not at greatly raised risk of genotoxic or other adverse outcomes as a consequence of their parent's treatment. The numbers of offspring assessed in the literature remains small, however, and surveillance of larger numbers of subjects is needed to enable reliable treatment-specific analyses.
doi_str_mv 10.1038/bjc.1996.355
format article
fullrecord <record><control><sourceid>springer</sourceid><recordid>TN_cdi_springer_journals_10_1038_bjc_1996_355</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1038_bjc_1996_355</sourcerecordid><originalsourceid>FETCH-springer_journals_10_1038_bjc_1996_3553</originalsourceid><addsrcrecordid>eNqVj81OhTAQhRujifiz8wFm5wawhSDg1nhzH8B9U-kARWhJp9zom_i4FvUFTCaZnMyZc_Ixdid4LnjZPLxNXS7a9jEvq-qMJaIqi0w0RX3OEs55nfG24JfsimiKsuVNnbCvA_pgZhM-U_C4eqe3LpgTgttC5xakFJTVMKKawwiuj9PT6o0d0l2tKhi0gSB4VAE19M7D0enh3dh7Am0IFeFTzABjT0jBDPHD7aqbNx1joBu9WxzFLsAPtRj7Y6AbdtGrmfD2b1-z7PDy-nzMftvRy8lt3saTFFzu-DLiyx1fRvzyv_5v_6dnJw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations: Clinical Oncology/Epidemiology</title><source>PubMed Central</source><creator>Swerdlow, AJ ; Jacobs, PA ; Marks, A ; Maher, EJ ; Young, T ; Barber, JCK ; Vaughan Hudson, G</creator><creatorcontrib>Swerdlow, AJ ; Jacobs, PA ; Marks, A ; Maher, EJ ; Young, T ; Barber, JCK ; Vaughan Hudson, G</creatorcontrib><description>Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionnaires to the patients. Eleven men and 16 women who had conceived any children after treatment were then interviewed. There was no excess of stillbirths, low birthweight or cogenital malformations, and no cancers have occurred in the 49 offspring after treatment. There was a significant excess of twins, compared with national expectations, in offspring of female patients (RR = 8.52, P = 0.025). Aggregation of series from the literature also showed an excess of twins. Chromosomes from cultures of peripheral lymphocytes from 45 children born to 25 patients (11 men and 14 women) after treatment were examined for numerical abnormalities and for structural abnormalities at the 550 or greater band level of resolution. All were normal except in one child with Down's syndrome (47, XY, +21), for whom we found the origin of the trisomy was from the parent without Hodgkin's disease. The chromosome constitution was also abnormal in one miscarriage (69, XXY; originating from the parent without Hodgkin's disease) and one termination (45, X; for with the parental origin could not be determined) after treatment. The study adds to previous questionnaire data and for the first time provides data also from chromosome analysis, that offspring of patients treated in adulthood for Hodgkin's disease are not at greatly raised risk of genotoxic or other adverse outcomes as a consequence of their parent's treatment. The numbers of offspring assessed in the literature remains small, however, and surveillance of larger numbers of subjects is needed to enable reliable treatment-specific analyses.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1996.355</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; clinical-oncology-epidemiology ; Drug Resistance ; Epidemiology ; Molecular Medicine ; Oncology</subject><ispartof>British journal of cancer, 1996-07, Vol.74 (2), p.291-296</ispartof><rights>Cancer Research Campaign 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Swerdlow, AJ</creatorcontrib><creatorcontrib>Jacobs, PA</creatorcontrib><creatorcontrib>Marks, A</creatorcontrib><creatorcontrib>Maher, EJ</creatorcontrib><creatorcontrib>Young, T</creatorcontrib><creatorcontrib>Barber, JCK</creatorcontrib><creatorcontrib>Vaughan Hudson, G</creatorcontrib><title>Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations: Clinical Oncology/Epidemiology</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionnaires to the patients. Eleven men and 16 women who had conceived any children after treatment were then interviewed. There was no excess of stillbirths, low birthweight or cogenital malformations, and no cancers have occurred in the 49 offspring after treatment. There was a significant excess of twins, compared with national expectations, in offspring of female patients (RR = 8.52, P = 0.025). Aggregation of series from the literature also showed an excess of twins. Chromosomes from cultures of peripheral lymphocytes from 45 children born to 25 patients (11 men and 14 women) after treatment were examined for numerical abnormalities and for structural abnormalities at the 550 or greater band level of resolution. All were normal except in one child with Down's syndrome (47, XY, +21), for whom we found the origin of the trisomy was from the parent without Hodgkin's disease. The chromosome constitution was also abnormal in one miscarriage (69, XXY; originating from the parent without Hodgkin's disease) and one termination (45, X; for with the parental origin could not be determined) after treatment. The study adds to previous questionnaire data and for the first time provides data also from chromosome analysis, that offspring of patients treated in adulthood for Hodgkin's disease are not at greatly raised risk of genotoxic or other adverse outcomes as a consequence of their parent's treatment. The numbers of offspring assessed in the literature remains small, however, and surveillance of larger numbers of subjects is needed to enable reliable treatment-specific analyses.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>clinical-oncology-epidemiology</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Molecular Medicine</subject><subject>Oncology</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqVj81OhTAQhRujifiz8wFm5wawhSDg1nhzH8B9U-kARWhJp9zom_i4FvUFTCaZnMyZc_Ixdid4LnjZPLxNXS7a9jEvq-qMJaIqi0w0RX3OEs55nfG24JfsimiKsuVNnbCvA_pgZhM-U_C4eqe3LpgTgttC5xakFJTVMKKawwiuj9PT6o0d0l2tKhi0gSB4VAE19M7D0enh3dh7Am0IFeFTzABjT0jBDPHD7aqbNx1joBu9WxzFLsAPtRj7Y6AbdtGrmfD2b1-z7PDy-nzMftvRy8lt3saTFFzu-DLiyx1fRvzyv_5v_6dnJw</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>Swerdlow, AJ</creator><creator>Jacobs, PA</creator><creator>Marks, A</creator><creator>Maher, EJ</creator><creator>Young, T</creator><creator>Barber, JCK</creator><creator>Vaughan Hudson, G</creator><general>Nature Publishing Group UK</general><scope/></search><sort><creationdate>19960701</creationdate><title>Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations</title><author>Swerdlow, AJ ; Jacobs, PA ; Marks, A ; Maher, EJ ; Young, T ; Barber, JCK ; Vaughan Hudson, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-springer_journals_10_1038_bjc_1996_3553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>clinical-oncology-epidemiology</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Molecular Medicine</topic><topic>Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Swerdlow, AJ</creatorcontrib><creatorcontrib>Jacobs, PA</creatorcontrib><creatorcontrib>Marks, A</creatorcontrib><creatorcontrib>Maher, EJ</creatorcontrib><creatorcontrib>Young, T</creatorcontrib><creatorcontrib>Barber, JCK</creatorcontrib><creatorcontrib>Vaughan Hudson, G</creatorcontrib><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Swerdlow, AJ</au><au>Jacobs, PA</au><au>Marks, A</au><au>Maher, EJ</au><au>Young, T</au><au>Barber, JCK</au><au>Vaughan Hudson, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations: Clinical Oncology/Epidemiology</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><date>1996-07-01</date><risdate>1996</risdate><volume>74</volume><issue>2</issue><spage>291</spage><epage>296</epage><pages>291-296</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><abstract>Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionnaires to the patients. Eleven men and 16 women who had conceived any children after treatment were then interviewed. There was no excess of stillbirths, low birthweight or cogenital malformations, and no cancers have occurred in the 49 offspring after treatment. There was a significant excess of twins, compared with national expectations, in offspring of female patients (RR = 8.52, P = 0.025). Aggregation of series from the literature also showed an excess of twins. Chromosomes from cultures of peripheral lymphocytes from 45 children born to 25 patients (11 men and 14 women) after treatment were examined for numerical abnormalities and for structural abnormalities at the 550 or greater band level of resolution. All were normal except in one child with Down's syndrome (47, XY, +21), for whom we found the origin of the trisomy was from the parent without Hodgkin's disease. The chromosome constitution was also abnormal in one miscarriage (69, XXY; originating from the parent without Hodgkin's disease) and one termination (45, X; for with the parental origin could not be determined) after treatment. The study adds to previous questionnaire data and for the first time provides data also from chromosome analysis, that offspring of patients treated in adulthood for Hodgkin's disease are not at greatly raised risk of genotoxic or other adverse outcomes as a consequence of their parent's treatment. The numbers of offspring assessed in the literature remains small, however, and surveillance of larger numbers of subjects is needed to enable reliable treatment-specific analyses.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/bjc.1996.355</doi></addata></record>
fulltext fulltext
identifier ISSN: 0007-0920
ispartof British journal of cancer, 1996-07, Vol.74 (2), p.291-296
issn 0007-0920
1532-1827
language eng
recordid cdi_springer_journals_10_1038_bjc_1996_355
source PubMed Central
subjects Biomedical and Life Sciences
Biomedicine
Cancer Research
clinical-oncology-epidemiology
Drug Resistance
Epidemiology
Molecular Medicine
Oncology
title Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations: Clinical Oncology/Epidemiology
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T08%3A12%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-springer&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fertility,%20reproductive%20outcomes,%20and%20health%20of%20offspring,%20of%20patients%20treated%20for%20Hodgkin's%20disease:%20an%20investigation%20including%20chromosome%20examinations:%20Clinical%20Oncology/Epidemiology&rft.jtitle=British%20journal%20of%20cancer&rft.au=Swerdlow,%20AJ&rft.date=1996-07-01&rft.volume=74&rft.issue=2&rft.spage=291&rft.epage=296&rft.pages=291-296&rft.issn=0007-0920&rft.eissn=1532-1827&rft_id=info:doi/10.1038/bjc.1996.355&rft_dat=%3Cspringer%3E10_1038_bjc_1996_355%3C/springer%3E%3Cgrp_id%3Ecdi_FETCH-springer_journals_10_1038_bjc_1996_3553%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true