4CPS-293 Efficacy and safety of cyclin dependent kinase inhibitors in metastatic breast cancer

Background and importanceCyclin dependent kinase inhibitors (CDKs) have demonstrated efficacy in the treatment of hormone receptor positive (RH+) and human epidermal growth factor receptor 2 (HER2-) metastatic breast cancer.Aim and objectivesTo evaluate the efficacy and safety of cyclin inhibitor dr...

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Veröffentlicht in:European journal of hospital pharmacy. Science and practice 2021-03, Vol.28 (Suppl 1), p.A61-A61
Hauptverfasser: Cantarelli, L, Morales Barrios, JA, Garcia Gil, S, Del Rosario Garcia, B, Nazco Casariego, GJ, Gutierrez Nicolas, F
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container_issue Suppl 1
container_start_page A61
container_title European journal of hospital pharmacy. Science and practice
container_volume 28
creator Cantarelli, L
Morales Barrios, JA
Garcia Gil, S
Del Rosario Garcia, B
Nazco Casariego, GJ
Gutierrez Nicolas, F
description Background and importanceCyclin dependent kinase inhibitors (CDKs) have demonstrated efficacy in the treatment of hormone receptor positive (RH+) and human epidermal growth factor receptor 2 (HER2-) metastatic breast cancer.Aim and objectivesTo evaluate the efficacy and safety of cyclin inhibitor drugs (CDK) in patients with metastatic breast cancer.Material and methodsAn 18 month, single centre, retrospective study (January 2019 to June 2020) that included all patients with metastatic breast cancer treated with palbociclib (PB), ribociclib (RB) and abemaciclib (AB) was conducted. The following variables were collected: age, sex, time of disease follow-up, time of treatment with the drug, neoadjuvant/adjuvant and previous hormonal therapy. Efficacy was evaluated by calculating progression free survival (PFS) for each drug, applying the Kaplan–Meier statistic. Progression was analysed according to the radiological criteria response evaluation criteria in solid tumours (RECIST V.1.1). The occurrence of adverse effects (AEs) leading to early dose reduction/suspension of the drug was analysed according to the common terminology criteria for adverse events (CTCAE).Results98 women (mean age 62.8 (34–86) years) were included in the study. 53.1% received PB (n=52), 25.5% (n=25) RB and 21.4% (n=21) AB. Mean follow-up time of the disease was 7.5 years. Mean duration of treatment was 9.5 months (0.1–34.3). 59.2% (n=58) received previous adjuvant therapy, 20.4% (n=20) neoadjuvant and 74.5% (n=73) hormonal.Median PFS wasAB vs PB (17.4 vs 11.9 months, p=0.008); AB vs RB (17.4 months vs not reached, p=0.065), PB vs RB (p=0.034). 34.7% (n=34) suspended treatment due to progression and 15.3% (n=15) due to toxicity. 54.1% (n=53) of patients had doses reduced due to AEs during treatment: PB (45.3%, n=24), RB (24.5%, n=13) and AB (30.2%, n=16). The most common AEs were: haematological (69.8%, n=37), gastrointestinal (17%, n=9), skin (9.4%, n=5), asthenic syndrome (9.4%, n=5), renal (5.7%, n=3), hepatic (5.7, n=3) and other (3.8%, n=2).Conclusion and relevancePFS was more favourable for AB than for PB, but not for RB. Likewise, RB treatment had a higher PFS than PB (p≤0.05). More than 50% of patients had their dose reduced due to the appearance of AEs, with PB being the least tolerated. This highlights the need for close monitoring of these AEs, which impairs long term efficacy.References and/or acknowledgementsConflict of interestNo conflict of interest
doi_str_mv 10.1136/ejhpharm-2021-eahpconf.125
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The following variables were collected: age, sex, time of disease follow-up, time of treatment with the drug, neoadjuvant/adjuvant and previous hormonal therapy. Efficacy was evaluated by calculating progression free survival (PFS) for each drug, applying the Kaplan–Meier statistic. Progression was analysed according to the radiological criteria response evaluation criteria in solid tumours (RECIST V.1.1). The occurrence of adverse effects (AEs) leading to early dose reduction/suspension of the drug was analysed according to the common terminology criteria for adverse events (CTCAE).Results98 women (mean age 62.8 (34–86) years) were included in the study. 53.1% received PB (n=52), 25.5% (n=25) RB and 21.4% (n=21) AB. Mean follow-up time of the disease was 7.5 years. Mean duration of treatment was 9.5 months (0.1–34.3). 59.2% (n=58) received previous adjuvant therapy, 20.4% (n=20) neoadjuvant and 74.5% (n=73) hormonal.Median PFS wasAB vs PB (17.4 vs 11.9 months, p=0.008); AB vs RB (17.4 months vs not reached, p=0.065), PB vs RB (p=0.034). 34.7% (n=34) suspended treatment due to progression and 15.3% (n=15) due to toxicity. 54.1% (n=53) of patients had doses reduced due to AEs during treatment: PB (45.3%, n=24), RB (24.5%, n=13) and AB (30.2%, n=16). The most common AEs were: haematological (69.8%, n=37), gastrointestinal (17%, n=9), skin (9.4%, n=5), asthenic syndrome (9.4%, n=5), renal (5.7%, n=3), hepatic (5.7, n=3) and other (3.8%, n=2).Conclusion and relevancePFS was more favourable for AB than for PB, but not for RB. Likewise, RB treatment had a higher PFS than PB (p≤0.05). More than 50% of patients had their dose reduced due to the appearance of AEs, with PB being the least tolerated. This highlights the need for close monitoring of these AEs, which impairs long term efficacy.References and/or acknowledgementsConflict of interestNo conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2021-eahpconf.125</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Breast cancer ; Conflicts of interest ; Drug dosages ; Metastasis</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2021-03, Vol.28 (Suppl 1), p.A61-A61</ispartof><rights>Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids></links><search><creatorcontrib>Cantarelli, L</creatorcontrib><creatorcontrib>Morales Barrios, JA</creatorcontrib><creatorcontrib>Garcia Gil, S</creatorcontrib><creatorcontrib>Del Rosario Garcia, B</creatorcontrib><creatorcontrib>Nazco Casariego, GJ</creatorcontrib><creatorcontrib>Gutierrez Nicolas, F</creatorcontrib><title>4CPS-293 Efficacy and safety of cyclin dependent kinase inhibitors in metastatic breast cancer</title><title>European journal of hospital pharmacy. Science and practice</title><description>Background and importanceCyclin dependent kinase inhibitors (CDKs) have demonstrated efficacy in the treatment of hormone receptor positive (RH+) and human epidermal growth factor receptor 2 (HER2-) metastatic breast cancer.Aim and objectivesTo evaluate the efficacy and safety of cyclin inhibitor drugs (CDK) in patients with metastatic breast cancer.Material and methodsAn 18 month, single centre, retrospective study (January 2019 to June 2020) that included all patients with metastatic breast cancer treated with palbociclib (PB), ribociclib (RB) and abemaciclib (AB) was conducted. The following variables were collected: age, sex, time of disease follow-up, time of treatment with the drug, neoadjuvant/adjuvant and previous hormonal therapy. Efficacy was evaluated by calculating progression free survival (PFS) for each drug, applying the Kaplan–Meier statistic. Progression was analysed according to the radiological criteria response evaluation criteria in solid tumours (RECIST V.1.1). The occurrence of adverse effects (AEs) leading to early dose reduction/suspension of the drug was analysed according to the common terminology criteria for adverse events (CTCAE).Results98 women (mean age 62.8 (34–86) years) were included in the study. 53.1% received PB (n=52), 25.5% (n=25) RB and 21.4% (n=21) AB. Mean follow-up time of the disease was 7.5 years. Mean duration of treatment was 9.5 months (0.1–34.3). 59.2% (n=58) received previous adjuvant therapy, 20.4% (n=20) neoadjuvant and 74.5% (n=73) hormonal.Median PFS wasAB vs PB (17.4 vs 11.9 months, p=0.008); AB vs RB (17.4 months vs not reached, p=0.065), PB vs RB (p=0.034). 34.7% (n=34) suspended treatment due to progression and 15.3% (n=15) due to toxicity. 54.1% (n=53) of patients had doses reduced due to AEs during treatment: PB (45.3%, n=24), RB (24.5%, n=13) and AB (30.2%, n=16). The most common AEs were: haematological (69.8%, n=37), gastrointestinal (17%, n=9), skin (9.4%, n=5), asthenic syndrome (9.4%, n=5), renal (5.7%, n=3), hepatic (5.7, n=3) and other (3.8%, n=2).Conclusion and relevancePFS was more favourable for AB than for PB, but not for RB. Likewise, RB treatment had a higher PFS than PB (p≤0.05). More than 50% of patients had their dose reduced due to the appearance of AEs, with PB being the least tolerated. This highlights the need for close monitoring of these AEs, which impairs long term efficacy.References and/or acknowledgementsConflict of interestNo conflict of interest</description><subject>Breast cancer</subject><subject>Conflicts of interest</subject><subject>Drug dosages</subject><subject>Metastasis</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kLtOwzAYhS0EElXpO1gwp9iOncQjqspFqgQSMJvfN8WlcYKTDtlYeFGehFRQpvMNR-dIH0KXlCwpzYtrt627GlKTMcJo5qDuTBv9kjJxgmaM8DKTsuCn_yyKc7To-6CJyPNK8lzO0BtfPT1nTObfn19r74MBM2KIFvfg3TDi1mMzml2I2LrORevigN9DhN7hEOugw9CmfkLcuAH6AYZgsE5uQmwgGpcu0JmHXe8WfzlHr7frl9V9tnm8e1jdbDJNWSEyKEvgWgP12lFmvBTWcFGVkpSVlazwXAMDziwpRWWhAKg4gDEFsd5yqvM5uvrd7VL7sXf9oLbtPsXpUjFBKJWMSzm1xG9LN1vVpdBAGhUl6uBTHX2qg0919Kkmn_kPZONv3A</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>Cantarelli, L</creator><creator>Morales Barrios, JA</creator><creator>Garcia Gil, S</creator><creator>Del Rosario Garcia, B</creator><creator>Nazco Casariego, GJ</creator><creator>Gutierrez Nicolas, F</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>202103</creationdate><title>4CPS-293 Efficacy and safety of cyclin dependent kinase inhibitors in metastatic breast cancer</title><author>Cantarelli, L ; Morales Barrios, JA ; Garcia Gil, S ; Del Rosario Garcia, B ; Nazco Casariego, GJ ; Gutierrez Nicolas, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1265-a77a4bba1fbe12cf95dc45879078d926f4ba2a42d0758da6aa84aacc60dfd41b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Breast cancer</topic><topic>Conflicts of interest</topic><topic>Drug dosages</topic><topic>Metastasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cantarelli, L</creatorcontrib><creatorcontrib>Morales Barrios, JA</creatorcontrib><creatorcontrib>Garcia Gil, S</creatorcontrib><creatorcontrib>Del Rosario Garcia, B</creatorcontrib><creatorcontrib>Nazco Casariego, GJ</creatorcontrib><creatorcontrib>Gutierrez Nicolas, F</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</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><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cantarelli, L</au><au>Morales Barrios, JA</au><au>Garcia Gil, S</au><au>Del Rosario Garcia, B</au><au>Nazco Casariego, GJ</au><au>Gutierrez Nicolas, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>4CPS-293 Efficacy and safety of cyclin dependent kinase inhibitors in metastatic breast cancer</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2021-03</date><risdate>2021</risdate><volume>28</volume><issue>Suppl 1</issue><spage>A61</spage><epage>A61</epage><pages>A61-A61</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>Background and importanceCyclin dependent kinase inhibitors (CDKs) have demonstrated efficacy in the treatment of hormone receptor positive (RH+) and human epidermal growth factor receptor 2 (HER2-) metastatic breast cancer.Aim and objectivesTo evaluate the efficacy and safety of cyclin inhibitor drugs (CDK) in patients with metastatic breast cancer.Material and methodsAn 18 month, single centre, retrospective study (January 2019 to June 2020) that included all patients with metastatic breast cancer treated with palbociclib (PB), ribociclib (RB) and abemaciclib (AB) was conducted. The following variables were collected: age, sex, time of disease follow-up, time of treatment with the drug, neoadjuvant/adjuvant and previous hormonal therapy. Efficacy was evaluated by calculating progression free survival (PFS) for each drug, applying the Kaplan–Meier statistic. Progression was analysed according to the radiological criteria response evaluation criteria in solid tumours (RECIST V.1.1). The occurrence of adverse effects (AEs) leading to early dose reduction/suspension of the drug was analysed according to the common terminology criteria for adverse events (CTCAE).Results98 women (mean age 62.8 (34–86) years) were included in the study. 53.1% received PB (n=52), 25.5% (n=25) RB and 21.4% (n=21) AB. Mean follow-up time of the disease was 7.5 years. Mean duration of treatment was 9.5 months (0.1–34.3). 59.2% (n=58) received previous adjuvant therapy, 20.4% (n=20) neoadjuvant and 74.5% (n=73) hormonal.Median PFS wasAB vs PB (17.4 vs 11.9 months, p=0.008); AB vs RB (17.4 months vs not reached, p=0.065), PB vs RB (p=0.034). 34.7% (n=34) suspended treatment due to progression and 15.3% (n=15) due to toxicity. 54.1% (n=53) of patients had doses reduced due to AEs during treatment: PB (45.3%, n=24), RB (24.5%, n=13) and AB (30.2%, n=16). The most common AEs were: haematological (69.8%, n=37), gastrointestinal (17%, n=9), skin (9.4%, n=5), asthenic syndrome (9.4%, n=5), renal (5.7%, n=3), hepatic (5.7, n=3) and other (3.8%, n=2).Conclusion and relevancePFS was more favourable for AB than for PB, but not for RB. Likewise, RB treatment had a higher PFS than PB (p≤0.05). More than 50% of patients had their dose reduced due to the appearance of AEs, with PB being the least tolerated. This highlights the need for close monitoring of these AEs, which impairs long term efficacy.References and/or acknowledgementsConflict of interestNo conflict of interest</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2021-eahpconf.125</doi><oa>free_for_read</oa></addata></record>
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subjects Breast cancer
Conflicts of interest
Drug dosages
Metastasis
title 4CPS-293 Efficacy and safety of cyclin dependent kinase inhibitors in metastatic breast cancer
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