Association of Menopausal Hormone Therapy With Breast Cancer Incidence and Mortality During Long-term Follow-up of the Women’s Health Initiative Randomized Clinical Trials

IMPORTANCE: The influence of menopausal hormone therapy on breast cancer remains unsettled with discordant findings from observational studies and randomized clinical trials. OBJECTIVE: To assess the association of prior randomized use of estrogen plus progestin or prior randomized use of estrogen a...

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Veröffentlicht in:JAMA : the journal of the American Medical Association 2020-07, Vol.324 (4), p.369-380
Hauptverfasser: Chlebowski, Rowan T, Anderson, Garnet L, Aragaki, Aaron K, Manson, JoAnn E, Stefanick, Marcia L, Pan, Kathy, Barrington, Wendy, Kuller, Lewis H, Simon, Michael S, Lane, Dorothy, Johnson, Karen C, Rohan, Thomas E, Gass, Margery L. S, Cauley, Jane A, Paskett, Electra D, Sattari, Maryam, Prentice, Ross L
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container_issue 4
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container_title JAMA : the journal of the American Medical Association
container_volume 324
creator Chlebowski, Rowan T
Anderson, Garnet L
Aragaki, Aaron K
Manson, JoAnn E
Stefanick, Marcia L
Pan, Kathy
Barrington, Wendy
Kuller, Lewis H
Simon, Michael S
Lane, Dorothy
Johnson, Karen C
Rohan, Thomas E
Gass, Margery L. S
Cauley, Jane A
Paskett, Electra D
Sattari, Maryam
Prentice, Ross L
description IMPORTANCE: The influence of menopausal hormone therapy on breast cancer remains unsettled with discordant findings from observational studies and randomized clinical trials. OBJECTIVE: To assess the association of prior randomized use of estrogen plus progestin or prior randomized use of estrogen alone with breast cancer incidence and mortality in the Women’s Health Initiative clinical trials. DESIGN, SETTING, AND PARTICIPANTS: Long-term follow-up of 2 placebo-controlled randomized clinical trials that involved 27 347 postmenopausal women aged 50 through 79 years with no prior breast cancer and negative baseline screening mammogram. Women were enrolled at 40 US centers from 1993 to 1998 with follow-up through December 31, 2017. INTERVENTIONS: In the trial involving 16 608 women with a uterus, 8506 were randomized to receive 0.625 mg/d of conjugated equine estrogen (CEE) plus 2.5 mg/d of medroxyprogesterone acetate (MPA) and 8102, placebo. In the trial involving 10 739 women with prior hysterectomy, 5310 were randomized to receive 0.625 mg/d of CEE alone and 5429, placebo. The CEE-plus-MPA trial was stopped in 2002 after 5.6 years’ median intervention duration, and the CEE-only trial was stopped in 2004 after 7.2 years’ median intervention duration. MAIN OUTCOMES AND MEASURES: The primary outcome was breast cancer incidence (protocol prespecified primary monitoring outcome for harm) and secondary outcomes were deaths from breast cancer and deaths after breast cancer. RESULTS: Among 27 347 postmenopausal women who were randomized in both trials (baseline mean [SD] age, 63.4 years [7.2 years]), after more than 20 years of median cumulative follow-up, mortality information was available for more than 98%. CEE alone compared with placebo among 10 739 women with a prior hysterectomy was associated with statistically significantly lower breast cancer incidence with 238 cases (annualized rate, 0.30%) vs 296 cases (annualized rate, 0.37%; hazard ratio [HR], 0.78; 95% CI, 0.65-0.93; P = .005) and was associated with statistically significantly lower breast cancer mortality with 30 deaths (annualized mortality rate, 0.031%) vs 46 deaths (annualized mortality rate, 0.046%; HR, 0.60; 95% CI, 0.37-0.97; P = .04). In contrast, CEE plus MPA compared with placebo among 16 608 women with a uterus was associated with statistically significantly higher breast cancer incidence with 584 cases (annualized rate, 0.45%) vs 447 cases (annualized rate, 0.36%; HR, 1.28; 95% CI, 1.13
doi_str_mv 10.1001/jama.2020.9482
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S ; Cauley, Jane A ; Paskett, Electra D ; Sattari, Maryam ; Prentice, Ross L</creator><creatorcontrib>Chlebowski, Rowan T ; Anderson, Garnet L ; Aragaki, Aaron K ; Manson, JoAnn E ; Stefanick, Marcia L ; Pan, Kathy ; Barrington, Wendy ; Kuller, Lewis H ; Simon, Michael S ; Lane, Dorothy ; Johnson, Karen C ; Rohan, Thomas E ; Gass, Margery L. S ; Cauley, Jane A ; Paskett, Electra D ; Sattari, Maryam ; Prentice, Ross L</creatorcontrib><description>IMPORTANCE: The influence of menopausal hormone therapy on breast cancer remains unsettled with discordant findings from observational studies and randomized clinical trials. OBJECTIVE: To assess the association of prior randomized use of estrogen plus progestin or prior randomized use of estrogen alone with breast cancer incidence and mortality in the Women’s Health Initiative clinical trials. DESIGN, SETTING, AND PARTICIPANTS: Long-term follow-up of 2 placebo-controlled randomized clinical trials that involved 27 347 postmenopausal women aged 50 through 79 years with no prior breast cancer and negative baseline screening mammogram. Women were enrolled at 40 US centers from 1993 to 1998 with follow-up through December 31, 2017. INTERVENTIONS: In the trial involving 16 608 women with a uterus, 8506 were randomized to receive 0.625 mg/d of conjugated equine estrogen (CEE) plus 2.5 mg/d of medroxyprogesterone acetate (MPA) and 8102, placebo. In the trial involving 10 739 women with prior hysterectomy, 5310 were randomized to receive 0.625 mg/d of CEE alone and 5429, placebo. The CEE-plus-MPA trial was stopped in 2002 after 5.6 years’ median intervention duration, and the CEE-only trial was stopped in 2004 after 7.2 years’ median intervention duration. MAIN OUTCOMES AND MEASURES: The primary outcome was breast cancer incidence (protocol prespecified primary monitoring outcome for harm) and secondary outcomes were deaths from breast cancer and deaths after breast cancer. RESULTS: Among 27 347 postmenopausal women who were randomized in both trials (baseline mean [SD] age, 63.4 years [7.2 years]), after more than 20 years of median cumulative follow-up, mortality information was available for more than 98%. CEE alone compared with placebo among 10 739 women with a prior hysterectomy was associated with statistically significantly lower breast cancer incidence with 238 cases (annualized rate, 0.30%) vs 296 cases (annualized rate, 0.37%; hazard ratio [HR], 0.78; 95% CI, 0.65-0.93; P = .005) and was associated with statistically significantly lower breast cancer mortality with 30 deaths (annualized mortality rate, 0.031%) vs 46 deaths (annualized mortality rate, 0.046%; HR, 0.60; 95% CI, 0.37-0.97; P = .04). In contrast, CEE plus MPA compared with placebo among 16 608 women with a uterus was associated with statistically significantly higher breast cancer incidence with 584 cases (annualized rate, 0.45%) vs 447 cases (annualized rate, 0.36%; HR, 1.28; 95% CI, 1.13-1.45; P &lt; .001) and no significant difference in breast cancer mortality with 71 deaths (annualized mortality rate, 0.045%) vs 53 deaths (annualized mortality rate, 0.035%; HR, 1.35; 95% CI, 0.94-1.95; P= .11). CONCLUSIONS AND RELEVANCE: In this long-term follow-up study of 2 randomized trials, prior randomized use of CEE alone, compared with placebo, among women who had a previous hysterectomy, was significantly associated with lower breast cancer incidence and lower breast cancer mortality, whereas prior randomized use of CEE plus MPA, compared with placebo, among women who had an intact uterus, was significantly associated with a higher breast cancer incidence but no significant difference in breast cancer mortality.</description><identifier>ISSN: 0098-7484</identifier><identifier>EISSN: 1538-3598</identifier><identifier>DOI: 10.1001/jama.2020.9482</identifier><identifier>PMID: 32721007</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><subject>Acetic acid ; Aged ; Breast cancer ; Breast Neoplasms - chemically induced ; Breast Neoplasms - epidemiology ; Breast Neoplasms - mortality ; Breast Neoplasms - prevention &amp; control ; Clinical trials ; Endocrine therapy ; Estrogens ; Estrogens, Conjugated (USP) - adverse effects ; Estrogens, Conjugated (USP) - therapeutic use ; Fatalities ; Female ; Follow-Up Studies ; Hormone replacement therapy ; Hormone Replacement Therapy - adverse effects ; Humans ; Hysterectomy ; Hysterectomy - adverse effects ; Incidence ; Mammography ; Medroxyprogesterone acetate ; Medroxyprogesterone Acetate - adverse effects ; Medroxyprogesterone Acetate - therapeutic use ; Menopause ; Middle Aged ; Mortality ; Original Investigation ; Post-menopause ; Postmenopause ; Progestin ; Randomization ; Risk ; Uterine cancer ; Uterus ; Womens health</subject><ispartof>JAMA : the journal of the American Medical Association, 2020-07, Vol.324 (4), p.369-380</ispartof><rights>Copyright American Medical Association Jul 28, 2020</rights><rights>Copyright 2020 American Medical Association. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a437t-24c8d0ad2b99df5a040b100c1ed0eeb7f62b822346b63bead7b2c44a550079d43</citedby><cites>FETCH-LOGICAL-a437t-24c8d0ad2b99df5a040b100c1ed0eeb7f62b822346b63bead7b2c44a550079d43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jama/articlepdf/10.1001/jama.2020.9482$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jama/fullarticle/10.1001/jama.2020.9482$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,230,314,776,780,881,3327,27901,27902,76231,76234</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32721007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chlebowski, Rowan T</creatorcontrib><creatorcontrib>Anderson, Garnet L</creatorcontrib><creatorcontrib>Aragaki, Aaron K</creatorcontrib><creatorcontrib>Manson, JoAnn E</creatorcontrib><creatorcontrib>Stefanick, Marcia L</creatorcontrib><creatorcontrib>Pan, Kathy</creatorcontrib><creatorcontrib>Barrington, Wendy</creatorcontrib><creatorcontrib>Kuller, Lewis H</creatorcontrib><creatorcontrib>Simon, Michael S</creatorcontrib><creatorcontrib>Lane, Dorothy</creatorcontrib><creatorcontrib>Johnson, Karen C</creatorcontrib><creatorcontrib>Rohan, Thomas E</creatorcontrib><creatorcontrib>Gass, Margery L. S</creatorcontrib><creatorcontrib>Cauley, Jane A</creatorcontrib><creatorcontrib>Paskett, Electra D</creatorcontrib><creatorcontrib>Sattari, Maryam</creatorcontrib><creatorcontrib>Prentice, Ross L</creatorcontrib><title>Association of Menopausal Hormone Therapy With Breast Cancer Incidence and Mortality During Long-term Follow-up of the Women’s Health Initiative Randomized Clinical Trials</title><title>JAMA : the journal of the American Medical Association</title><addtitle>JAMA</addtitle><description>IMPORTANCE: The influence of menopausal hormone therapy on breast cancer remains unsettled with discordant findings from observational studies and randomized clinical trials. OBJECTIVE: To assess the association of prior randomized use of estrogen plus progestin or prior randomized use of estrogen alone with breast cancer incidence and mortality in the Women’s Health Initiative clinical trials. DESIGN, SETTING, AND PARTICIPANTS: Long-term follow-up of 2 placebo-controlled randomized clinical trials that involved 27 347 postmenopausal women aged 50 through 79 years with no prior breast cancer and negative baseline screening mammogram. Women were enrolled at 40 US centers from 1993 to 1998 with follow-up through December 31, 2017. INTERVENTIONS: In the trial involving 16 608 women with a uterus, 8506 were randomized to receive 0.625 mg/d of conjugated equine estrogen (CEE) plus 2.5 mg/d of medroxyprogesterone acetate (MPA) and 8102, placebo. In the trial involving 10 739 women with prior hysterectomy, 5310 were randomized to receive 0.625 mg/d of CEE alone and 5429, placebo. The CEE-plus-MPA trial was stopped in 2002 after 5.6 years’ median intervention duration, and the CEE-only trial was stopped in 2004 after 7.2 years’ median intervention duration. MAIN OUTCOMES AND MEASURES: The primary outcome was breast cancer incidence (protocol prespecified primary monitoring outcome for harm) and secondary outcomes were deaths from breast cancer and deaths after breast cancer. RESULTS: Among 27 347 postmenopausal women who were randomized in both trials (baseline mean [SD] age, 63.4 years [7.2 years]), after more than 20 years of median cumulative follow-up, mortality information was available for more than 98%. CEE alone compared with placebo among 10 739 women with a prior hysterectomy was associated with statistically significantly lower breast cancer incidence with 238 cases (annualized rate, 0.30%) vs 296 cases (annualized rate, 0.37%; hazard ratio [HR], 0.78; 95% CI, 0.65-0.93; P = .005) and was associated with statistically significantly lower breast cancer mortality with 30 deaths (annualized mortality rate, 0.031%) vs 46 deaths (annualized mortality rate, 0.046%; HR, 0.60; 95% CI, 0.37-0.97; P = .04). In contrast, CEE plus MPA compared with placebo among 16 608 women with a uterus was associated with statistically significantly higher breast cancer incidence with 584 cases (annualized rate, 0.45%) vs 447 cases (annualized rate, 0.36%; HR, 1.28; 95% CI, 1.13-1.45; P &lt; .001) and no significant difference in breast cancer mortality with 71 deaths (annualized mortality rate, 0.045%) vs 53 deaths (annualized mortality rate, 0.035%; HR, 1.35; 95% CI, 0.94-1.95; P= .11). CONCLUSIONS AND RELEVANCE: In this long-term follow-up study of 2 randomized trials, prior randomized use of CEE alone, compared with placebo, among women who had a previous hysterectomy, was significantly associated with lower breast cancer incidence and lower breast cancer mortality, whereas prior randomized use of CEE plus MPA, compared with placebo, among women who had an intact uterus, was significantly associated with a higher breast cancer incidence but no significant difference in breast cancer mortality.</description><subject>Acetic acid</subject><subject>Aged</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - chemically induced</subject><subject>Breast Neoplasms - epidemiology</subject><subject>Breast Neoplasms - mortality</subject><subject>Breast Neoplasms - prevention &amp; control</subject><subject>Clinical trials</subject><subject>Endocrine therapy</subject><subject>Estrogens</subject><subject>Estrogens, Conjugated (USP) - adverse effects</subject><subject>Estrogens, Conjugated (USP) - therapeutic use</subject><subject>Fatalities</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hormone replacement therapy</subject><subject>Hormone Replacement Therapy - adverse effects</subject><subject>Humans</subject><subject>Hysterectomy</subject><subject>Hysterectomy - adverse effects</subject><subject>Incidence</subject><subject>Mammography</subject><subject>Medroxyprogesterone acetate</subject><subject>Medroxyprogesterone Acetate - adverse effects</subject><subject>Medroxyprogesterone Acetate - therapeutic use</subject><subject>Menopause</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Original Investigation</subject><subject>Post-menopause</subject><subject>Postmenopause</subject><subject>Progestin</subject><subject>Randomization</subject><subject>Risk</subject><subject>Uterine cancer</subject><subject>Uterus</subject><subject>Womens health</subject><issn>0098-7484</issn><issn>1538-3598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1vEzEQtRCIhsKVAwdkifMGr-39uiCV0JJIqZBQUI_W7O5s4mjXDra3KD3xN_gR_Cl-CV6lrcCXsTTvvXkzj5DXKZunjKXv9zDAnDPO5pUs-RMySzNRJiKryqdkxlhVJoUs5Rl54f2exZeK4jk5E7zgkV7MyO8L722jIWhrqO3oNRp7gNFDT5fWDdYg3ezQweFIb3TY0Y8OwQe6ANOgoyvT6Bbjl4Jp6bV1AXodjvTT6LTZ0rU12ySgG-iV7Xv7IxkP04ywQ3pjBzR_fv7ydInQR-GV0WGycYv0axSzg77Dli56bXQTzWycht6_JM-6WPDVfT0n364uN4tlsv7yebW4WCcgRRESLpuyZdDyuqraLgMmWR3XbVJsGWJddDmvS86FzOtc1AhtUfNGSsiyeJOqleKcfDjpHsZ6wLZBExz06uD0AO6oLGj1f8fondraW1WIsmQ8jwLv7gWc_T6iD2pvR2eiZ8WlyDLJmeARNT-hGme9d9g9TkiZmuJVU7xqildN8UbC2399PcIf8oyANyfAxHvo8iKPrnLxF7AFrnU</recordid><startdate>20200728</startdate><enddate>20200728</enddate><creator>Chlebowski, Rowan T</creator><creator>Anderson, Garnet L</creator><creator>Aragaki, Aaron K</creator><creator>Manson, JoAnn E</creator><creator>Stefanick, Marcia L</creator><creator>Pan, Kathy</creator><creator>Barrington, Wendy</creator><creator>Kuller, Lewis H</creator><creator>Simon, Michael S</creator><creator>Lane, Dorothy</creator><creator>Johnson, Karen C</creator><creator>Rohan, Thomas E</creator><creator>Gass, Margery L. 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S</creatorcontrib><creatorcontrib>Cauley, Jane A</creatorcontrib><creatorcontrib>Paskett, Electra D</creatorcontrib><creatorcontrib>Sattari, Maryam</creatorcontrib><creatorcontrib>Prentice, Ross L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JAMA : the journal of the American Medical Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chlebowski, Rowan T</au><au>Anderson, Garnet L</au><au>Aragaki, Aaron K</au><au>Manson, JoAnn E</au><au>Stefanick, Marcia L</au><au>Pan, Kathy</au><au>Barrington, Wendy</au><au>Kuller, Lewis H</au><au>Simon, Michael S</au><au>Lane, Dorothy</au><au>Johnson, Karen C</au><au>Rohan, Thomas E</au><au>Gass, Margery L. S</au><au>Cauley, Jane A</au><au>Paskett, Electra D</au><au>Sattari, Maryam</au><au>Prentice, Ross L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of Menopausal Hormone Therapy With Breast Cancer Incidence and Mortality During Long-term Follow-up of the Women’s Health Initiative Randomized Clinical Trials</atitle><jtitle>JAMA : the journal of the American Medical Association</jtitle><addtitle>JAMA</addtitle><date>2020-07-28</date><risdate>2020</risdate><volume>324</volume><issue>4</issue><spage>369</spage><epage>380</epage><pages>369-380</pages><issn>0098-7484</issn><eissn>1538-3598</eissn><abstract>IMPORTANCE: The influence of menopausal hormone therapy on breast cancer remains unsettled with discordant findings from observational studies and randomized clinical trials. OBJECTIVE: To assess the association of prior randomized use of estrogen plus progestin or prior randomized use of estrogen alone with breast cancer incidence and mortality in the Women’s Health Initiative clinical trials. DESIGN, SETTING, AND PARTICIPANTS: Long-term follow-up of 2 placebo-controlled randomized clinical trials that involved 27 347 postmenopausal women aged 50 through 79 years with no prior breast cancer and negative baseline screening mammogram. Women were enrolled at 40 US centers from 1993 to 1998 with follow-up through December 31, 2017. INTERVENTIONS: In the trial involving 16 608 women with a uterus, 8506 were randomized to receive 0.625 mg/d of conjugated equine estrogen (CEE) plus 2.5 mg/d of medroxyprogesterone acetate (MPA) and 8102, placebo. In the trial involving 10 739 women with prior hysterectomy, 5310 were randomized to receive 0.625 mg/d of CEE alone and 5429, placebo. The CEE-plus-MPA trial was stopped in 2002 after 5.6 years’ median intervention duration, and the CEE-only trial was stopped in 2004 after 7.2 years’ median intervention duration. MAIN OUTCOMES AND MEASURES: The primary outcome was breast cancer incidence (protocol prespecified primary monitoring outcome for harm) and secondary outcomes were deaths from breast cancer and deaths after breast cancer. RESULTS: Among 27 347 postmenopausal women who were randomized in both trials (baseline mean [SD] age, 63.4 years [7.2 years]), after more than 20 years of median cumulative follow-up, mortality information was available for more than 98%. CEE alone compared with placebo among 10 739 women with a prior hysterectomy was associated with statistically significantly lower breast cancer incidence with 238 cases (annualized rate, 0.30%) vs 296 cases (annualized rate, 0.37%; hazard ratio [HR], 0.78; 95% CI, 0.65-0.93; P = .005) and was associated with statistically significantly lower breast cancer mortality with 30 deaths (annualized mortality rate, 0.031%) vs 46 deaths (annualized mortality rate, 0.046%; HR, 0.60; 95% CI, 0.37-0.97; P = .04). In contrast, CEE plus MPA compared with placebo among 16 608 women with a uterus was associated with statistically significantly higher breast cancer incidence with 584 cases (annualized rate, 0.45%) vs 447 cases (annualized rate, 0.36%; HR, 1.28; 95% CI, 1.13-1.45; P &lt; .001) and no significant difference in breast cancer mortality with 71 deaths (annualized mortality rate, 0.045%) vs 53 deaths (annualized mortality rate, 0.035%; HR, 1.35; 95% CI, 0.94-1.95; P= .11). CONCLUSIONS AND RELEVANCE: In this long-term follow-up study of 2 randomized trials, prior randomized use of CEE alone, compared with placebo, among women who had a previous hysterectomy, was significantly associated with lower breast cancer incidence and lower breast cancer mortality, whereas prior randomized use of CEE plus MPA, compared with placebo, among women who had an intact uterus, was significantly associated with a higher breast cancer incidence but no significant difference in breast cancer mortality.</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>32721007</pmid><doi>10.1001/jama.2020.9482</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0098-7484
ispartof JAMA : the journal of the American Medical Association, 2020-07, Vol.324 (4), p.369-380
issn 0098-7484
1538-3598
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7388026
source MEDLINE; American Medical Association Journals
subjects Acetic acid
Aged
Breast cancer
Breast Neoplasms - chemically induced
Breast Neoplasms - epidemiology
Breast Neoplasms - mortality
Breast Neoplasms - prevention & control
Clinical trials
Endocrine therapy
Estrogens
Estrogens, Conjugated (USP) - adverse effects
Estrogens, Conjugated (USP) - therapeutic use
Fatalities
Female
Follow-Up Studies
Hormone replacement therapy
Hormone Replacement Therapy - adverse effects
Humans
Hysterectomy
Hysterectomy - adverse effects
Incidence
Mammography
Medroxyprogesterone acetate
Medroxyprogesterone Acetate - adverse effects
Medroxyprogesterone Acetate - therapeutic use
Menopause
Middle Aged
Mortality
Original Investigation
Post-menopause
Postmenopause
Progestin
Randomization
Risk
Uterine cancer
Uterus
Womens health
title Association of Menopausal Hormone Therapy With Breast Cancer Incidence and Mortality During Long-term Follow-up of the Women’s Health Initiative Randomized Clinical Trials
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