Incidence and risk factors for congestive heart failure in patients with early breast cancer who received anthracycline and/or trastuzumab: a big data analysis of the Korean Health Insurance Review and Assessment service database

Purpose We aimed to analyze the incidence, time to occurrence, and congestive heart failure (CHF) risk factors for early breast cancer patients treated with anthracycline (AC)-based chemotherapy and/or trastuzumab (T) therapy in Korea. Methods We included female patients > 19 years old from the H...

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Veröffentlicht in:Breast cancer research and treatment 2018-08, Vol.171 (1), p.181-188
Hauptverfasser: Choi, Jung Yoon, Cho, Eun Young, Choi, Yoon Ji, Lee, Jeong Hyeon, Jung, Seung Pil, Cho, Kyu Ran, Kim, Chul Yong, Kim, Yeul Hong, Park, Kyong Hwa
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container_issue 1
container_start_page 181
container_title Breast cancer research and treatment
container_volume 171
creator Choi, Jung Yoon
Cho, Eun Young
Choi, Yoon Ji
Lee, Jeong Hyeon
Jung, Seung Pil
Cho, Kyu Ran
Kim, Chul Yong
Kim, Yeul Hong
Park, Kyong Hwa
description Purpose We aimed to analyze the incidence, time to occurrence, and congestive heart failure (CHF) risk factors for early breast cancer patients treated with anthracycline (AC)-based chemotherapy and/or trastuzumab (T) therapy in Korea. Methods We included female patients > 19 years old from the Health Insurance Review and Assessment Service database who had no prior CHF history and had been diagnosed with early breast cancer between January 2007 and October 2016. Results We included 83,544 patients in our analysis. In terms of crude incidence for CHF, AC followed by T showed the highest incidence (6.3%). However, 3.1 and 4.2% of the patients had CHF due to AC-based chemotherapy and non-AC followed by T, respectively. The median times to occurrence of CHF were different according to adjuvant treatments, approximately 2 years (701.0 days) in the AC-based chemotherapy group vs 1 year (377.5 days) AC followed by T group. T therapy was associated with earlier development of CHF irrespective of previous chemotherapy, but late risk of CHF 1.2 years after T therapy rapidly decreased in both chemotherapy groups. Multivariate Cox regression analysis revealed that the adjusted hazard ratio for CHF was increased in the group of older patients (≥ 65 years old) who underwent AC followed by T therapy, with Charlson comorbidity index scores of ≥ 2. Conclusions Our study showed that neo-/adjuvant chemotherapy using T irrespective of previous chemotherapy (AC or non-AC) was associated with significantly increased risk of CHF compared with AC-based chemotherapy in Korean patients with early breast cancer.
doi_str_mv 10.1007/s10549-018-4809-8
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Methods We included female patients &gt; 19 years old from the Health Insurance Review and Assessment Service database who had no prior CHF history and had been diagnosed with early breast cancer between January 2007 and October 2016. Results We included 83,544 patients in our analysis. In terms of crude incidence for CHF, AC followed by T showed the highest incidence (6.3%). However, 3.1 and 4.2% of the patients had CHF due to AC-based chemotherapy and non-AC followed by T, respectively. The median times to occurrence of CHF were different according to adjuvant treatments, approximately 2 years (701.0 days) in the AC-based chemotherapy group vs 1 year (377.5 days) AC followed by T group. T therapy was associated with earlier development of CHF irrespective of previous chemotherapy, but late risk of CHF 1.2 years after T therapy rapidly decreased in both chemotherapy groups. Multivariate Cox regression analysis revealed that the adjusted hazard ratio for CHF was increased in the group of older patients (≥ 65 years old) who underwent AC followed by T therapy, with Charlson comorbidity index scores of ≥ 2. Conclusions Our study showed that neo-/adjuvant chemotherapy using T irrespective of previous chemotherapy (AC or non-AC) was associated with significantly increased risk of CHF compared with AC-based chemotherapy in Korean patients with early breast cancer.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-018-4809-8</identifier><identifier>PMID: 29737474</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adjuvant chemotherapy ; Adult ; Aged ; Aged, 80 and over ; Anthracycline ; Anthracyclines ; Anthracyclines - administration &amp; dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Big Data ; Breast cancer ; Breast Neoplasms - complications ; Breast Neoplasms - drug therapy ; Breast Neoplasms - epidemiology ; Breast Neoplasms - pathology ; Cancer patients ; Cancer research ; Cancer therapies ; Cardiac patients ; Chemotherapy ; Comorbidity ; Congestive heart failure ; Databases, Factual ; Development and progression ; Epidemiology ; Female ; Heart failure ; Heart Failure - epidemiology ; Heart Failure - etiology ; Humans ; Immunotherapy ; Incidence ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Monoclonal antibodies ; Oncology ; Proportional Hazards Models ; Public Health Surveillance ; Risk Assessment ; Risk Factors ; Targeted cancer therapy ; Trastuzumab ; Trastuzumab - administration &amp; dosage</subject><ispartof>Breast cancer research and treatment, 2018-08, Vol.171 (1), p.181-188</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-ecce0a19b716a70a1d3f02ebeb3846fb8a11bf933514c032b9555d429c0dc0353</citedby><cites>FETCH-LOGICAL-c470t-ecce0a19b716a70a1d3f02ebeb3846fb8a11bf933514c032b9555d429c0dc0353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10549-018-4809-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-018-4809-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29737474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Jung Yoon</creatorcontrib><creatorcontrib>Cho, Eun Young</creatorcontrib><creatorcontrib>Choi, Yoon Ji</creatorcontrib><creatorcontrib>Lee, Jeong Hyeon</creatorcontrib><creatorcontrib>Jung, Seung Pil</creatorcontrib><creatorcontrib>Cho, Kyu Ran</creatorcontrib><creatorcontrib>Kim, Chul Yong</creatorcontrib><creatorcontrib>Kim, Yeul Hong</creatorcontrib><creatorcontrib>Park, Kyong Hwa</creatorcontrib><title>Incidence and risk factors for congestive heart failure in patients with early breast cancer who received anthracycline and/or trastuzumab: a big data analysis of the Korean Health Insurance Review and Assessment service database</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose We aimed to analyze the incidence, time to occurrence, and congestive heart failure (CHF) risk factors for early breast cancer patients treated with anthracycline (AC)-based chemotherapy and/or trastuzumab (T) therapy in Korea. Methods We included female patients &gt; 19 years old from the Health Insurance Review and Assessment Service database who had no prior CHF history and had been diagnosed with early breast cancer between January 2007 and October 2016. Results We included 83,544 patients in our analysis. In terms of crude incidence for CHF, AC followed by T showed the highest incidence (6.3%). However, 3.1 and 4.2% of the patients had CHF due to AC-based chemotherapy and non-AC followed by T, respectively. The median times to occurrence of CHF were different according to adjuvant treatments, approximately 2 years (701.0 days) in the AC-based chemotherapy group vs 1 year (377.5 days) AC followed by T group. T therapy was associated with earlier development of CHF irrespective of previous chemotherapy, but late risk of CHF 1.2 years after T therapy rapidly decreased in both chemotherapy groups. Multivariate Cox regression analysis revealed that the adjusted hazard ratio for CHF was increased in the group of older patients (≥ 65 years old) who underwent AC followed by T therapy, with Charlson comorbidity index scores of ≥ 2. Conclusions Our study showed that neo-/adjuvant chemotherapy using T irrespective of previous chemotherapy (AC or non-AC) was associated with significantly increased risk of CHF compared with AC-based chemotherapy in Korean patients with early breast cancer.</description><subject>Adjuvant chemotherapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anthracycline</subject><subject>Anthracyclines</subject><subject>Anthracyclines - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Big Data</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - complications</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - epidemiology</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer patients</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Cardiac patients</subject><subject>Chemotherapy</subject><subject>Comorbidity</subject><subject>Congestive heart failure</subject><subject>Databases, Factual</subject><subject>Development and progression</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Heart failure</subject><subject>Heart Failure - epidemiology</subject><subject>Heart Failure - etiology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Incidence</subject><subject>Medicine</subject><subject>Medicine &amp; 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Methods We included female patients &gt; 19 years old from the Health Insurance Review and Assessment Service database who had no prior CHF history and had been diagnosed with early breast cancer between January 2007 and October 2016. Results We included 83,544 patients in our analysis. In terms of crude incidence for CHF, AC followed by T showed the highest incidence (6.3%). However, 3.1 and 4.2% of the patients had CHF due to AC-based chemotherapy and non-AC followed by T, respectively. The median times to occurrence of CHF were different according to adjuvant treatments, approximately 2 years (701.0 days) in the AC-based chemotherapy group vs 1 year (377.5 days) AC followed by T group. T therapy was associated with earlier development of CHF irrespective of previous chemotherapy, but late risk of CHF 1.2 years after T therapy rapidly decreased in both chemotherapy groups. Multivariate Cox regression analysis revealed that the adjusted hazard ratio for CHF was increased in the group of older patients (≥ 65 years old) who underwent AC followed by T therapy, with Charlson comorbidity index scores of ≥ 2. Conclusions Our study showed that neo-/adjuvant chemotherapy using T irrespective of previous chemotherapy (AC or non-AC) was associated with significantly increased risk of CHF compared with AC-based chemotherapy in Korean patients with early breast cancer.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29737474</pmid><doi>10.1007/s10549-018-4809-8</doi><tpages>8</tpages></addata></record>
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subjects Adjuvant chemotherapy
Adult
Aged
Aged, 80 and over
Anthracycline
Anthracyclines
Anthracyclines - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Big Data
Breast cancer
Breast Neoplasms - complications
Breast Neoplasms - drug therapy
Breast Neoplasms - epidemiology
Breast Neoplasms - pathology
Cancer patients
Cancer research
Cancer therapies
Cardiac patients
Chemotherapy
Comorbidity
Congestive heart failure
Databases, Factual
Development and progression
Epidemiology
Female
Heart failure
Heart Failure - epidemiology
Heart Failure - etiology
Humans
Immunotherapy
Incidence
Medicine
Medicine & Public Health
Middle Aged
Monoclonal antibodies
Oncology
Proportional Hazards Models
Public Health Surveillance
Risk Assessment
Risk Factors
Targeted cancer therapy
Trastuzumab
Trastuzumab - administration & dosage
title Incidence and risk factors for congestive heart failure in patients with early breast cancer who received anthracycline and/or trastuzumab: a big data analysis of the Korean Health Insurance Review and Assessment service database
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