The impact of fertility preservation on the timing of breast cancer treatment, recurrence, and survival

Background Many young women with breast cancer undergo fertility preservation (FP) before cancer treatment. This study examined the impact of FP on breast cancer outcomes. Methods The authors performed a retrospective cohort study of 272 women aged 20 to 45 years with newly diagnosed stage 0 to III...

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Veröffentlicht in:Cancer 2021-10, Vol.127 (20), p.3872-3880
Hauptverfasser: Greer, Anna C., Lanes, Andrea, Poorvu, Philip D., Kennedy, Patricia, Thomas, Ann M., Partridge, Ann H., Ginsburg, Elizabeth S.
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container_end_page 3880
container_issue 20
container_start_page 3872
container_title Cancer
container_volume 127
creator Greer, Anna C.
Lanes, Andrea
Poorvu, Philip D.
Kennedy, Patricia
Thomas, Ann M.
Partridge, Ann H.
Ginsburg, Elizabeth S.
description Background Many young women with breast cancer undergo fertility preservation (FP) before cancer treatment. This study examined the impact of FP on breast cancer outcomes. Methods The authors performed a retrospective cohort study of 272 women aged 20 to 45 years with newly diagnosed stage 0 to III breast cancer who underwent an FP consultation between 2005 and 2017. Among these women, 123 (45.2%) underwent FP (fertility preservation–positive [FP+]). The remaining 149 women did not undergo FP (fertility preservation–negative [FP–]). Results The characteristics at enrollment were similar with the exception of ethnicity (FP+, 87.8% White; FP–, 67.8% White; P = .002) and BRCA status (FP+, 27.7% BRCA+; FP–, 15.5% BRCA+; P = .021). The median follow‐up was approximately 4 years. Women who underwent FP had longer times to first treatment (FP+, 37 days; FP–, 31 days; adjusted hazard ratio [aHR], 0.74; confidence interval [CI], 0.56‐0.99) and neoadjuvant chemotherapy (FP+, 36 days; FP–, 26 days; aHR, 0.41; CI, 0.24‐0.68) and from surgery to adjuvant chemotherapy (FP+, 41 days; FP–, 33 days; aHR, 0.58; CI, 0.38‐0.90). Adjusted 3‐ and 5‐year invasive disease–free survival (IDFS) rates were comparable between the 2 groups (3‐year IDFS: FP+, 85.4%; FP–, 79.4%; P = .411; 5‐year IDFS: FP+, 73.7%; FP–, 67.1%; P = .288). Similarly, no difference in overall survival (OS) was observed between the 2 groups (3‐year OS: FP+, 95.5%; FP–, 93.5%; P = .854; 5‐year OS: FP+, 84.2%; FP–, 81.4%; P = .700). Conclusions FP after a breast cancer diagnosis delays the time to treatment by a small amount, but this delay does not lead to inferior IDFS or OS. Controlled ovarian stimulation for the purpose of fertility preservation in patients with breast cancer delays the initiation of systemic treatment but does not affect recurrence or survival. Fertility preservation provides a safe option for women diagnosed with breast cancer who are facing gonadotoxic treatment regimens and desire future fertility.
doi_str_mv 10.1002/cncr.33601
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This study examined the impact of FP on breast cancer outcomes. Methods The authors performed a retrospective cohort study of 272 women aged 20 to 45 years with newly diagnosed stage 0 to III breast cancer who underwent an FP consultation between 2005 and 2017. Among these women, 123 (45.2%) underwent FP (fertility preservation–positive [FP+]). The remaining 149 women did not undergo FP (fertility preservation–negative [FP–]). Results The characteristics at enrollment were similar with the exception of ethnicity (FP+, 87.8% White; FP–, 67.8% White; P = .002) and BRCA status (FP+, 27.7% BRCA+; FP–, 15.5% BRCA+; P = .021). The median follow‐up was approximately 4 years. Women who underwent FP had longer times to first treatment (FP+, 37 days; FP–, 31 days; adjusted hazard ratio [aHR], 0.74; confidence interval [CI], 0.56‐0.99) and neoadjuvant chemotherapy (FP+, 36 days; FP–, 26 days; aHR, 0.41; CI, 0.24‐0.68) and from surgery to adjuvant chemotherapy (FP+, 41 days; FP–, 33 days; aHR, 0.58; CI, 0.38‐0.90). Adjusted 3‐ and 5‐year invasive disease–free survival (IDFS) rates were comparable between the 2 groups (3‐year IDFS: FP+, 85.4%; FP–, 79.4%; P = .411; 5‐year IDFS: FP+, 73.7%; FP–, 67.1%; P = .288). Similarly, no difference in overall survival (OS) was observed between the 2 groups (3‐year OS: FP+, 95.5%; FP–, 93.5%; P = .854; 5‐year OS: FP+, 84.2%; FP–, 81.4%; P = .700). Conclusions FP after a breast cancer diagnosis delays the time to treatment by a small amount, but this delay does not lead to inferior IDFS or OS. Controlled ovarian stimulation for the purpose of fertility preservation in patients with breast cancer delays the initiation of systemic treatment but does not affect recurrence or survival. Fertility preservation provides a safe option for women diagnosed with breast cancer who are facing gonadotoxic treatment regimens and desire future fertility.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.33601</identifier><identifier>PMID: 34161610</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Breast cancer ; Breast Neoplasms - drug therapy ; Cancer therapies ; Chemotherapy ; Chemotherapy, Adjuvant ; Confidence intervals ; Female ; Fertility ; Fertility Preservation ; Humans ; Invasiveness ; Middle Aged ; Minority &amp; ethnic groups ; Neoadjuvant Therapy ; Oncology ; oocyte cryopreservation ; Preservation ; Retrospective Studies ; Survival ; survivorship ; treatment outcomes ; Young Adult</subject><ispartof>Cancer, 2021-10, Vol.127 (20), p.3872-3880</ispartof><rights>2021 American Cancer Society</rights><rights>2021 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3931-a5b3c2a1f74c7f1e9292e6f18114f5ad68fc6d40ced9ec4ee2a3a66679d138523</citedby><cites>FETCH-LOGICAL-c3931-a5b3c2a1f74c7f1e9292e6f18114f5ad68fc6d40ced9ec4ee2a3a66679d138523</cites><orcidid>0000-0002-5097-4917 ; 0000-0002-4722-4824</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.33601$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.33601$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34161610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Greer, Anna C.</creatorcontrib><creatorcontrib>Lanes, Andrea</creatorcontrib><creatorcontrib>Poorvu, Philip D.</creatorcontrib><creatorcontrib>Kennedy, Patricia</creatorcontrib><creatorcontrib>Thomas, Ann M.</creatorcontrib><creatorcontrib>Partridge, Ann H.</creatorcontrib><creatorcontrib>Ginsburg, Elizabeth S.</creatorcontrib><title>The impact of fertility preservation on the timing of breast cancer treatment, recurrence, and survival</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Background Many young women with breast cancer undergo fertility preservation (FP) before cancer treatment. This study examined the impact of FP on breast cancer outcomes. Methods The authors performed a retrospective cohort study of 272 women aged 20 to 45 years with newly diagnosed stage 0 to III breast cancer who underwent an FP consultation between 2005 and 2017. Among these women, 123 (45.2%) underwent FP (fertility preservation–positive [FP+]). The remaining 149 women did not undergo FP (fertility preservation–negative [FP–]). Results The characteristics at enrollment were similar with the exception of ethnicity (FP+, 87.8% White; FP–, 67.8% White; P = .002) and BRCA status (FP+, 27.7% BRCA+; FP–, 15.5% BRCA+; P = .021). The median follow‐up was approximately 4 years. Women who underwent FP had longer times to first treatment (FP+, 37 days; FP–, 31 days; adjusted hazard ratio [aHR], 0.74; confidence interval [CI], 0.56‐0.99) and neoadjuvant chemotherapy (FP+, 36 days; FP–, 26 days; aHR, 0.41; CI, 0.24‐0.68) and from surgery to adjuvant chemotherapy (FP+, 41 days; FP–, 33 days; aHR, 0.58; CI, 0.38‐0.90). Adjusted 3‐ and 5‐year invasive disease–free survival (IDFS) rates were comparable between the 2 groups (3‐year IDFS: FP+, 85.4%; FP–, 79.4%; P = .411; 5‐year IDFS: FP+, 73.7%; FP–, 67.1%; P = .288). Similarly, no difference in overall survival (OS) was observed between the 2 groups (3‐year OS: FP+, 95.5%; FP–, 93.5%; P = .854; 5‐year OS: FP+, 84.2%; FP–, 81.4%; P = .700). Conclusions FP after a breast cancer diagnosis delays the time to treatment by a small amount, but this delay does not lead to inferior IDFS or OS. Controlled ovarian stimulation for the purpose of fertility preservation in patients with breast cancer delays the initiation of systemic treatment but does not affect recurrence or survival. Fertility preservation provides a safe option for women diagnosed with breast cancer who are facing gonadotoxic treatment regimens and desire future fertility.</description><subject>Adult</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Confidence intervals</subject><subject>Female</subject><subject>Fertility</subject><subject>Fertility Preservation</subject><subject>Humans</subject><subject>Invasiveness</subject><subject>Middle Aged</subject><subject>Minority &amp; ethnic groups</subject><subject>Neoadjuvant Therapy</subject><subject>Oncology</subject><subject>oocyte cryopreservation</subject><subject>Preservation</subject><subject>Retrospective Studies</subject><subject>Survival</subject><subject>survivorship</subject><subject>treatment outcomes</subject><subject>Young Adult</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMoWqsXf4AEvIh0a742u3uU4heIglTwtqTZSY3sR02ylf57U1s9eJAZGGZ4eBhehE4oGVNC2KVutRtzLgndQQNKiiwhVLBdNCCE5Ekq-OsBOvT-Pa4ZS_k-OuCCylhkgObTN8C2WSgdcGewARdsbcMKLxx4cEsVbNfi2CFywTa2na-5mQPlA9aq1eBwiFtooA0j7ED3zkE8j7BqK-x7t7RLVR-hPaNqD8fbOUQvN9fTyV3y8HR7P7l6SDQvOE1UOuOaKWoyoTNDoWAFA2loTqkwqapkbrSsBNFQFaAFAFNcSSmzoqI8TxkfovONd-G6jx58KBvrNdS1aqHrfclSIfKskCSL6Nkf9L3rXRu_i1QWnXlarIUXG0q7znsHplw42yi3Kikp1_GX6_jL7_gjfLpV9rMGql_0J-8I0A3waWtY_aMqJ4-T5430C13XkDI</recordid><startdate>20211015</startdate><enddate>20211015</enddate><creator>Greer, Anna C.</creator><creator>Lanes, Andrea</creator><creator>Poorvu, Philip D.</creator><creator>Kennedy, Patricia</creator><creator>Thomas, Ann M.</creator><creator>Partridge, Ann H.</creator><creator>Ginsburg, Elizabeth S.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5097-4917</orcidid><orcidid>https://orcid.org/0000-0002-4722-4824</orcidid></search><sort><creationdate>20211015</creationdate><title>The impact of fertility preservation on the timing of breast cancer treatment, recurrence, and survival</title><author>Greer, Anna C. ; Lanes, Andrea ; Poorvu, Philip D. ; Kennedy, Patricia ; Thomas, Ann M. ; Partridge, Ann H. ; Ginsburg, Elizabeth S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3931-a5b3c2a1f74c7f1e9292e6f18114f5ad68fc6d40ced9ec4ee2a3a66679d138523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Confidence intervals</topic><topic>Female</topic><topic>Fertility</topic><topic>Fertility Preservation</topic><topic>Humans</topic><topic>Invasiveness</topic><topic>Middle Aged</topic><topic>Minority &amp; ethnic groups</topic><topic>Neoadjuvant Therapy</topic><topic>Oncology</topic><topic>oocyte cryopreservation</topic><topic>Preservation</topic><topic>Retrospective Studies</topic><topic>Survival</topic><topic>survivorship</topic><topic>treatment outcomes</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Greer, Anna C.</creatorcontrib><creatorcontrib>Lanes, Andrea</creatorcontrib><creatorcontrib>Poorvu, Philip D.</creatorcontrib><creatorcontrib>Kennedy, Patricia</creatorcontrib><creatorcontrib>Thomas, Ann M.</creatorcontrib><creatorcontrib>Partridge, Ann H.</creatorcontrib><creatorcontrib>Ginsburg, Elizabeth S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Greer, Anna C.</au><au>Lanes, Andrea</au><au>Poorvu, Philip D.</au><au>Kennedy, Patricia</au><au>Thomas, Ann M.</au><au>Partridge, Ann H.</au><au>Ginsburg, Elizabeth S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of fertility preservation on the timing of breast cancer treatment, recurrence, and survival</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2021-10-15</date><risdate>2021</risdate><volume>127</volume><issue>20</issue><spage>3872</spage><epage>3880</epage><pages>3872-3880</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>Background Many young women with breast cancer undergo fertility preservation (FP) before cancer treatment. This study examined the impact of FP on breast cancer outcomes. Methods The authors performed a retrospective cohort study of 272 women aged 20 to 45 years with newly diagnosed stage 0 to III breast cancer who underwent an FP consultation between 2005 and 2017. Among these women, 123 (45.2%) underwent FP (fertility preservation–positive [FP+]). The remaining 149 women did not undergo FP (fertility preservation–negative [FP–]). Results The characteristics at enrollment were similar with the exception of ethnicity (FP+, 87.8% White; FP–, 67.8% White; P = .002) and BRCA status (FP+, 27.7% BRCA+; FP–, 15.5% BRCA+; P = .021). The median follow‐up was approximately 4 years. Women who underwent FP had longer times to first treatment (FP+, 37 days; FP–, 31 days; adjusted hazard ratio [aHR], 0.74; confidence interval [CI], 0.56‐0.99) and neoadjuvant chemotherapy (FP+, 36 days; FP–, 26 days; aHR, 0.41; CI, 0.24‐0.68) and from surgery to adjuvant chemotherapy (FP+, 41 days; FP–, 33 days; aHR, 0.58; CI, 0.38‐0.90). Adjusted 3‐ and 5‐year invasive disease–free survival (IDFS) rates were comparable between the 2 groups (3‐year IDFS: FP+, 85.4%; FP–, 79.4%; P = .411; 5‐year IDFS: FP+, 73.7%; FP–, 67.1%; P = .288). Similarly, no difference in overall survival (OS) was observed between the 2 groups (3‐year OS: FP+, 95.5%; FP–, 93.5%; P = .854; 5‐year OS: FP+, 84.2%; FP–, 81.4%; P = .700). Conclusions FP after a breast cancer diagnosis delays the time to treatment by a small amount, but this delay does not lead to inferior IDFS or OS. Controlled ovarian stimulation for the purpose of fertility preservation in patients with breast cancer delays the initiation of systemic treatment but does not affect recurrence or survival. Fertility preservation provides a safe option for women diagnosed with breast cancer who are facing gonadotoxic treatment regimens and desire future fertility.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34161610</pmid><doi>10.1002/cncr.33601</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5097-4917</orcidid><orcidid>https://orcid.org/0000-0002-4722-4824</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Breast cancer
Breast Neoplasms - drug therapy
Cancer therapies
Chemotherapy
Chemotherapy, Adjuvant
Confidence intervals
Female
Fertility
Fertility Preservation
Humans
Invasiveness
Middle Aged
Minority & ethnic groups
Neoadjuvant Therapy
Oncology
oocyte cryopreservation
Preservation
Retrospective Studies
Survival
survivorship
treatment outcomes
Young Adult
title The impact of fertility preservation on the timing of breast cancer treatment, recurrence, and survival
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