Prognostic characteristics in hormone receptor-positive advanced breast cancer and characterization of abemaciclib efficacy
CDK4 & 6 inhibitors have enhanced the effectiveness of endocrine therapy (ET) in patients with advanced breast cancer (ABC). This paper presents exploratory analyses examining patient and disease characteristics that may inform in whom and when abemaciclib should be initiated. MONARCH 2 and 3 en...
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creator | Di Leo, Angelo O’Shaughnessy, Joyce Sledge, George W. Martin, Miguel Lin, Yong Frenzel, Martin Hardebeck, Molly C. Smith, Ian C. Llombart-Cussac, Antonio Goetz, Matthew P. Johnston, Stephen |
description | CDK4 & 6 inhibitors have enhanced the effectiveness of endocrine therapy (ET) in patients with advanced breast cancer (ABC). This paper presents exploratory analyses examining patient and disease characteristics that may inform in whom and when abemaciclib should be initiated. MONARCH 2 and 3 enrolled women with HR+, HER2- ABC. In MONARCH 2, patients whose disease had progressed while receiving ET were administered fulvestrant+abemaciclib/placebo. In MONARCH 3, patients received a nonsteroidal aromatase inhibitor+abemaciclib/placebo as initial therapy for advanced disease. A combined analysis of the two studies was performed to determine significant prognostic factors. Efficacy results (PFS and ORR in patients with measurable disease) were examined for patient subgroups corresponding to each significant prognostic factor. Analysis of clinical factors confirmed the following to have prognostic value: bone-only disease, liver metastases, tumor grade, progesterone receptor status, performance status, treatment-free interval (TFI) from the end of adjuvant ET, and time from diagnosis to recurrence. Prognosis was poorer in patients with liver metastases, progesterone receptor-negative tumors, high grade tumors, or short TFI (20 months. These analyses identified prognostic factors and demonstrated that patients with poor prognostic factors derived the largest benefit from the addition of abemaciclib.
Biomarkers: Prognostic factors indicate likely beneficiaries of cell cycle–blocking therapy
A series of clinical factors may help identify those patients with hormone receptor-positive breast cancer who are most likely to benefit from a newly approved cell cycle–blocking drug. Angelo Di Leo from the Hospital of Prato, Italy, and colleagues retrospectively analyzed data from two phase III trials that evaluated the CDK4 & 6 inhibitor abemaciclib against a placebo administered in combination with either fulvestrant endocrine therapy or an aromatase inhibitor. Pooling the results, the researchers found that patients with certain indicators of poor prognosis—including liver metastases, progesterone receptor negativity, high-grad |
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Biomarkers: Prognostic factors indicate likely beneficiaries of cell cycle–blocking therapy
A series of clinical factors may help identify those patients with hormone receptor-positive breast cancer who are most likely to benefit from a newly approved cell cycle–blocking drug. Angelo Di Leo from the Hospital of Prato, Italy, and colleagues retrospectively analyzed data from two phase III trials that evaluated the CDK4 & 6 inhibitor abemaciclib against a placebo administered in combination with either fulvestrant endocrine therapy or an aromatase inhibitor. Pooling the results, the researchers found that patients with certain indicators of poor prognosis—including liver metastases, progesterone receptor negativity, high-grade tumors, or short treatment-free intervals following the completion of adjuvant endocrine therapy—benefited most from abemaciclib, as measured by progression-free survival. The findings, if confirmed in prospective trials, could help inform personalized drug choices for patients.</description><identifier>ISSN: 2374-4677</identifier><identifier>EISSN: 2374-4677</identifier><identifier>DOI: 10.1038/s41523-018-0094-2</identifier><identifier>PMID: 30588487</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/308/53/2422 ; 692/4028/67/1347 ; Biomedical and Life Sciences ; Biomedicine ; Breast cancer ; Cancer Research ; Cell Biology ; Human Genetics ; Medical prognosis ; Metastasis ; Oncology ; Patients ; Tumors</subject><ispartof>NPJ breast cancer, 2018-12, Vol.4 (1), p.41-8, Article 41</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-1b54ff31ad88b5e46693c18f08d3761b357f11914a9b38ce94004ebb755650593</citedby><cites>FETCH-LOGICAL-c470t-1b54ff31ad88b5e46693c18f08d3761b357f11914a9b38ce94004ebb755650593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299082/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299082/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,41118,42187,51574,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30588487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Leo, Angelo</creatorcontrib><creatorcontrib>O’Shaughnessy, Joyce</creatorcontrib><creatorcontrib>Sledge, George W.</creatorcontrib><creatorcontrib>Martin, Miguel</creatorcontrib><creatorcontrib>Lin, Yong</creatorcontrib><creatorcontrib>Frenzel, Martin</creatorcontrib><creatorcontrib>Hardebeck, Molly C.</creatorcontrib><creatorcontrib>Smith, Ian C.</creatorcontrib><creatorcontrib>Llombart-Cussac, Antonio</creatorcontrib><creatorcontrib>Goetz, Matthew P.</creatorcontrib><creatorcontrib>Johnston, Stephen</creatorcontrib><title>Prognostic characteristics in hormone receptor-positive advanced breast cancer and characterization of abemaciclib efficacy</title><title>NPJ breast cancer</title><addtitle>npj Breast Cancer</addtitle><addtitle>NPJ Breast Cancer</addtitle><description>CDK4 & 6 inhibitors have enhanced the effectiveness of endocrine therapy (ET) in patients with advanced breast cancer (ABC). This paper presents exploratory analyses examining patient and disease characteristics that may inform in whom and when abemaciclib should be initiated. MONARCH 2 and 3 enrolled women with HR+, HER2- ABC. In MONARCH 2, patients whose disease had progressed while receiving ET were administered fulvestrant+abemaciclib/placebo. In MONARCH 3, patients received a nonsteroidal aromatase inhibitor+abemaciclib/placebo as initial therapy for advanced disease. A combined analysis of the two studies was performed to determine significant prognostic factors. Efficacy results (PFS and ORR in patients with measurable disease) were examined for patient subgroups corresponding to each significant prognostic factor. Analysis of clinical factors confirmed the following to have prognostic value: bone-only disease, liver metastases, tumor grade, progesterone receptor status, performance status, treatment-free interval (TFI) from the end of adjuvant ET, and time from diagnosis to recurrence. Prognosis was poorer in patients with liver metastases, progesterone receptor-negative tumors, high grade tumors, or short TFI (<36 months). Benefit (PFS hazard ratio, ORR increase) from abemaciclib was observed in all patient subgroups. Patients with indicators of poor prognosis had the largest benefit from the addition of abemaciclib. However, in MONARCH 3, for patients with certain good prognostic factors (TFI ≥ 36 months, bone-only disease) ET achieved a median PFS of >20 months. These analyses identified prognostic factors and demonstrated that patients with poor prognostic factors derived the largest benefit from the addition of abemaciclib.
Biomarkers: Prognostic factors indicate likely beneficiaries of cell cycle–blocking therapy
A series of clinical factors may help identify those patients with hormone receptor-positive breast cancer who are most likely to benefit from a newly approved cell cycle–blocking drug. Angelo Di Leo from the Hospital of Prato, Italy, and colleagues retrospectively analyzed data from two phase III trials that evaluated the CDK4 & 6 inhibitor abemaciclib against a placebo administered in combination with either fulvestrant endocrine therapy or an aromatase inhibitor. Pooling the results, the researchers found that patients with certain indicators of poor prognosis—including liver metastases, progesterone receptor negativity, high-grade tumors, or short treatment-free intervals following the completion of adjuvant endocrine therapy—benefited most from abemaciclib, as measured by progression-free survival. 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O’Shaughnessy, Joyce ; Sledge, George W. ; Martin, Miguel ; Lin, Yong ; Frenzel, Martin ; Hardebeck, Molly C. ; Smith, Ian C. ; Llombart-Cussac, Antonio ; Goetz, Matthew P. ; Johnston, Stephen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-1b54ff31ad88b5e46693c18f08d3761b357f11914a9b38ce94004ebb755650593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>692/308/53/2422</topic><topic>692/4028/67/1347</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Breast cancer</topic><topic>Cancer Research</topic><topic>Cell Biology</topic><topic>Human Genetics</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Oncology</topic><topic>Patients</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Leo, Angelo</creatorcontrib><creatorcontrib>O’Shaughnessy, Joyce</creatorcontrib><creatorcontrib>Sledge, George W.</creatorcontrib><creatorcontrib>Martin, Miguel</creatorcontrib><creatorcontrib>Lin, Yong</creatorcontrib><creatorcontrib>Frenzel, Martin</creatorcontrib><creatorcontrib>Hardebeck, Molly C.</creatorcontrib><creatorcontrib>Smith, Ian C.</creatorcontrib><creatorcontrib>Llombart-Cussac, Antonio</creatorcontrib><creatorcontrib>Goetz, Matthew P.</creatorcontrib><creatorcontrib>Johnston, Stephen</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>NPJ breast cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Leo, Angelo</au><au>O’Shaughnessy, Joyce</au><au>Sledge, George W.</au><au>Martin, Miguel</au><au>Lin, Yong</au><au>Frenzel, Martin</au><au>Hardebeck, Molly C.</au><au>Smith, Ian C.</au><au>Llombart-Cussac, Antonio</au><au>Goetz, Matthew P.</au><au>Johnston, Stephen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic characteristics in hormone receptor-positive advanced breast cancer and characterization of abemaciclib efficacy</atitle><jtitle>NPJ breast cancer</jtitle><stitle>npj Breast Cancer</stitle><addtitle>NPJ Breast Cancer</addtitle><date>2018-12-18</date><risdate>2018</risdate><volume>4</volume><issue>1</issue><spage>41</spage><epage>8</epage><pages>41-8</pages><artnum>41</artnum><issn>2374-4677</issn><eissn>2374-4677</eissn><abstract>CDK4 & 6 inhibitors have enhanced the effectiveness of endocrine therapy (ET) in patients with advanced breast cancer (ABC). This paper presents exploratory analyses examining patient and disease characteristics that may inform in whom and when abemaciclib should be initiated. MONARCH 2 and 3 enrolled women with HR+, HER2- ABC. In MONARCH 2, patients whose disease had progressed while receiving ET were administered fulvestrant+abemaciclib/placebo. In MONARCH 3, patients received a nonsteroidal aromatase inhibitor+abemaciclib/placebo as initial therapy for advanced disease. A combined analysis of the two studies was performed to determine significant prognostic factors. Efficacy results (PFS and ORR in patients with measurable disease) were examined for patient subgroups corresponding to each significant prognostic factor. Analysis of clinical factors confirmed the following to have prognostic value: bone-only disease, liver metastases, tumor grade, progesterone receptor status, performance status, treatment-free interval (TFI) from the end of adjuvant ET, and time from diagnosis to recurrence. Prognosis was poorer in patients with liver metastases, progesterone receptor-negative tumors, high grade tumors, or short TFI (<36 months). Benefit (PFS hazard ratio, ORR increase) from abemaciclib was observed in all patient subgroups. Patients with indicators of poor prognosis had the largest benefit from the addition of abemaciclib. However, in MONARCH 3, for patients with certain good prognostic factors (TFI ≥ 36 months, bone-only disease) ET achieved a median PFS of >20 months. These analyses identified prognostic factors and demonstrated that patients with poor prognostic factors derived the largest benefit from the addition of abemaciclib.
Biomarkers: Prognostic factors indicate likely beneficiaries of cell cycle–blocking therapy
A series of clinical factors may help identify those patients with hormone receptor-positive breast cancer who are most likely to benefit from a newly approved cell cycle–blocking drug. Angelo Di Leo from the Hospital of Prato, Italy, and colleagues retrospectively analyzed data from two phase III trials that evaluated the CDK4 & 6 inhibitor abemaciclib against a placebo administered in combination with either fulvestrant endocrine therapy or an aromatase inhibitor. Pooling the results, the researchers found that patients with certain indicators of poor prognosis—including liver metastases, progesterone receptor negativity, high-grade tumors, or short treatment-free intervals following the completion of adjuvant endocrine therapy—benefited most from abemaciclib, as measured by progression-free survival. The findings, if confirmed in prospective trials, could help inform personalized drug choices for patients.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30588487</pmid><doi>10.1038/s41523-018-0094-2</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/308/53/2422 692/4028/67/1347 Biomedical and Life Sciences Biomedicine Breast cancer Cancer Research Cell Biology Human Genetics Medical prognosis Metastasis Oncology Patients Tumors |
title | Prognostic characteristics in hormone receptor-positive advanced breast cancer and characterization of abemaciclib efficacy |
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