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Efficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy

Background There is no standard treatment recommended at category 1 level in international guidelines for subsequent therapy after cyclin-dependent kinase 4/6 inhibitor (CDK4/6) based therapy. We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression und...

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Published in:BMC Cancer 2023, Vol.23 (1)
Main Authors: Karacin, Cengiz, Oksuzoglu, Berna, Demirci, AyÅe, Keskinkiliç, Merve, Baytemür, Naziyet Köse, Yilmaz, Funda, Selvi, OÄuzhan, Erdem, Dilek, AvÅar, Esin, Paksoy, Nail, Demir, Necla, Göksu, Sema Sezgin, Türker, Sema, Bayram, ErtuÄrul, Çelebi, Abdüssamet, Yilmaz, Hatice, Kuzu, ümer Faruk, Kahraman, Seda, Gökmen, Ä°vo, Sakin, Abdullah, Alkan, Ali, Nayir, Erdinç, UÄrakli, Muzaffer, Acar, ümer, Ertürk, Ä°smail, Demir, Hacer, Aslan, Ferit, Sönmez, üzlem, Korkmaz, Taner, Celayir, üzde Melisa, KaradaÄ, Ä°brahim, KayikçioÄlu, Erkan, Åakalar, Teoman, üktem, Ä°lker Nihat, Eren, Tülay, Urul, Enes, Mocan, Eda Eylemer, Kalkan, Ziya, Yildirim, Nilgün, Ergün, Yakup, Akagündüz, Baran, Karakaya, Serdar, Kut, Engin, Teker, Fatih, Demirel, Burçin Çakan, Karaboyun, Kubilay, Almuradova, Elvina, Ãnal, Olçun Ãmit, Oyman, Abdilkerim, IÅik, Deniz, Okutur, Kerem, üztosun, BuÄra, GülbaÄci, Burcu Belen, Kalender, Mehmet Emin, Åahin, Elif, Seyyar, Mustafa, üzdemir, üzlem, Selçukbiricik, Fatih, Kanitez, Metin, Dede, Ä°sa, GümüÅ, Mahmut, Gökmen, Erhan, Yaren, Arzu, MenekÅe, Serkan, Ebinç, Senar, Aksoy, Sercan, Ä°mamoÄlu, GökÅen Ä°nanç, AltinbaÅ, Mustafa, Çetin, Bülent, Uluç, BaÅak Oyan, Er, üzlem, KaradurmuÅ, Nuri, ErdoÄan, Atike Pinar, Artaç, Mehmet, Tanriverdi, üzgür, Çiçin, Ä°rfan, Åendur, Mehmet Ali Nahit, Oktay, Esin, BayoÄlu, Ä°brahim Vedat, PaydaÅ, Semra, Aydiner, Adnan, Salim, Derya Kivrak, Geredeli, ÇaÄlayan, YavuzÅen, TuÄba, DoÄan, Mutlu, HacibekiroÄlu, Ä°lhan
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container_title BMC Cancer
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creator Karacin, Cengiz
Oksuzoglu, Berna
Demirci, AyÅe
Keskinkiliç, Merve
Baytemür, Naziyet Köse
Yilmaz, Funda
Selvi, OÄuzhan
Erdem, Dilek
AvÅar, Esin
Paksoy, Nail
Demir, Necla
Göksu, Sema Sezgin
Türker, Sema
Bayram, ErtuÄrul
Çelebi, Abdüssamet
Yilmaz, Hatice
Kuzu, ümer Faruk
Kahraman, Seda
Gökmen, Ä°vo
Sakin, Abdullah
Alkan, Ali
Nayir, Erdinç
UÄrakli, Muzaffer
Acar, ümer
Ertürk, Ä°smail
Demir, Hacer
Aslan, Ferit
Sönmez, üzlem
Korkmaz, Taner
Celayir, üzde Melisa
KaradaÄ, Ä°brahim
KayikçioÄlu, Erkan
Åakalar, Teoman
üktem, Ä°lker Nihat
Eren, Tülay
Urul, Enes
Mocan, Eda Eylemer
Kalkan, Ziya
Yildirim, Nilgün
Ergün, Yakup
Akagündüz, Baran
Karakaya, Serdar
Kut, Engin
Teker, Fatih
Demirel, Burçin Çakan
Karaboyun, Kubilay
Almuradova, Elvina
Ãnal, Olçun Ãmit
Oyman, Abdilkerim
IÅik, Deniz
Okutur, Kerem
üztosun, BuÄra
GülbaÄci, Burcu Belen
Kalender, Mehmet Emin
Åahin, Elif
Seyyar, Mustafa
üzdemir, üzlem
Selçukbiricik, Fatih
Kanitez, Metin
Dede, Ä°sa
GümüÅ, Mahmut
Gökmen, Erhan
Yaren, Arzu
MenekÅe, Serkan
Ebinç, Senar
Aksoy, Sercan
Ä°mamoÄlu, GökÅen Ä°nanç
AltinbaÅ, Mustafa
Çetin, Bülent
Uluç, BaÅak Oyan
Er, üzlem
KaradurmuÅ, Nuri
ErdoÄan, Atike Pinar
Artaç, Mehmet
Tanriverdi, üzgür
Çiçin, Ä°rfan
Åendur, Mehmet Ali Nahit
Oktay, Esin
BayoÄlu, Ä°brahim Vedat
PaydaÅ, Semra
Aydiner, Adnan
Salim, Derya Kivrak
Geredeli, ÇaÄlayan
YavuzÅen, TuÄba
DoÄan, Mutlu
HacibekiroÄlu, Ä°lhan
description Background There is no standard treatment recommended at category 1 level in international guidelines for subsequent therapy after cyclin-dependent kinase 4/6 inhibitor (CDK4/6) based therapy. We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression under CDKi. In addition, we aimed to show the effectiveness of systemic treatments after CDKi and whether there is a survival difference between hormonal treatments (monotherapy vs. mTOR-based). Methods A total of 609 patients from 53 centers were included in the study. Progression-free-survivals (PFS) of subsequent treatments (chemotherapy (CT, n:434) or endocrine therapy (ET, n:175)) after CDKi were calculated. Patients were evaluated in three groups as those who received CDKi in first-line (group A, n:202), second-line (group B, n: 153) and [greater than or equal to] 3rd-line (group C, n: 254). PFS was compared according to the use of ET and CT. In addition, ET was compared as monotherapy versus everolimus-based combination therapy. Results The median duration of CDKi in the ET arms of Group A, B, and C was 17.0, 11.0, and 8.5 months in respectively; it was 9.0, 7.0, and 5.0 months in the CT arm. Median PFS after CDKi was 9.5 (5.0-14.0) months in the ET arm of group A, and 5.3 (3.9-6.8) months in the CT arm (p = 0.073). It was 6.7 (5.8-7.7) months in the ET arm of group B, and 5.7 (4.6-6.7) months in the CT arm (p = 0.311). It was 5.3 (2.5-8.0) months in the ET arm of group C and 4.0 (3.5-4.6) months in the CT arm (p = 0.434). Patients who received ET after CDKi were compared as those who received everolimus-based combination therapy versus those who received monotherapy ET: the median PFS in group A, B, and C was 11.0 vs. 5.9 (p = 0.047), 6.7 vs. 5.0 (p = 0.164), 6.7 vs. 3.9 (p = 0.763) months. Conclusion Physicians preferred CT rather than ET in patients with early progression under CDKi. It has been shown that subsequent ET after CDKi can be as effective as CT. It was also observed that better PFS could be achieved with the subsequent everolimus-based treatments after first-line CDKi compared to monotherapy ET. Keywords: Advanced breast cancer, Cyclin-dependent kinase, Ribociclib, Palbociclib, Everolimus, Fulvestrant, Endocrine treatment, Hormonotherapy
doi_str_mv 10.1186/s12885-023-10609-8
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We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression under CDKi. In addition, we aimed to show the effectiveness of systemic treatments after CDKi and whether there is a survival difference between hormonal treatments (monotherapy vs. mTOR-based). Methods A total of 609 patients from 53 centers were included in the study. Progression-free-survivals (PFS) of subsequent treatments (chemotherapy (CT, n:434) or endocrine therapy (ET, n:175)) after CDKi were calculated. Patients were evaluated in three groups as those who received CDKi in first-line (group A, n:202), second-line (group B, n: 153) and [greater than or equal to] 3rd-line (group C, n: 254). PFS was compared according to the use of ET and CT. In addition, ET was compared as monotherapy versus everolimus-based combination therapy. Results The median duration of CDKi in the ET arms of Group A, B, and C was 17.0, 11.0, and 8.5 months in respectively; it was 9.0, 7.0, and 5.0 months in the CT arm. Median PFS after CDKi was 9.5 (5.0-14.0) months in the ET arm of group A, and 5.3 (3.9-6.8) months in the CT arm (p = 0.073). It was 6.7 (5.8-7.7) months in the ET arm of group B, and 5.7 (4.6-6.7) months in the CT arm (p = 0.311). It was 5.3 (2.5-8.0) months in the ET arm of group C and 4.0 (3.5-4.6) months in the CT arm (p = 0.434). Patients who received ET after CDKi were compared as those who received everolimus-based combination therapy versus those who received monotherapy ET: the median PFS in group A, B, and C was 11.0 vs. 5.9 (p = 0.047), 6.7 vs. 5.0 (p = 0.164), 6.7 vs. 3.9 (p = 0.763) months. Conclusion Physicians preferred CT rather than ET in patients with early progression under CDKi. It has been shown that subsequent ET after CDKi can be as effective as CT. It was also observed that better PFS could be achieved with the subsequent everolimus-based treatments after first-line CDKi compared to monotherapy ET. Keywords: Advanced breast cancer, Cyclin-dependent kinase, Ribociclib, Palbociclib, Everolimus, Fulvestrant, Endocrine treatment, Hormonotherapy</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-023-10609-8</identifier><language>eng</language><publisher>BioMed Central Ltd</publisher><subject>Analysis ; Antimitotic agents ; Antineoplastic agents ; Breast cancer ; Cancer ; Care and treatment ; Chemotherapy ; Cyclins ; Development and progression ; Dosage and administration ; Hormone therapy ; Patient outcomes</subject><ispartof>BMC Cancer, 2023, Vol.23 (1)</ispartof><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27901</link.rule.ids></links><search><creatorcontrib>Karacin, Cengiz</creatorcontrib><creatorcontrib>Oksuzoglu, Berna</creatorcontrib><creatorcontrib>Demirci, AyÅe</creatorcontrib><creatorcontrib>Keskinkiliç, Merve</creatorcontrib><creatorcontrib>Baytemür, Naziyet Köse</creatorcontrib><creatorcontrib>Yilmaz, Funda</creatorcontrib><creatorcontrib>Selvi, OÄuzhan</creatorcontrib><creatorcontrib>Erdem, Dilek</creatorcontrib><creatorcontrib>AvÅar, Esin</creatorcontrib><creatorcontrib>Paksoy, Nail</creatorcontrib><creatorcontrib>Demir, Necla</creatorcontrib><creatorcontrib>Göksu, Sema Sezgin</creatorcontrib><creatorcontrib>Türker, Sema</creatorcontrib><creatorcontrib>Bayram, ErtuÄrul</creatorcontrib><creatorcontrib>Çelebi, Abdüssamet</creatorcontrib><creatorcontrib>Yilmaz, Hatice</creatorcontrib><creatorcontrib>Kuzu, ümer Faruk</creatorcontrib><creatorcontrib>Kahraman, Seda</creatorcontrib><creatorcontrib>Gökmen, Ä°vo</creatorcontrib><creatorcontrib>Sakin, Abdullah</creatorcontrib><creatorcontrib>Alkan, Ali</creatorcontrib><creatorcontrib>Nayir, Erdinç</creatorcontrib><creatorcontrib>UÄrakli, Muzaffer</creatorcontrib><creatorcontrib>Acar, ümer</creatorcontrib><creatorcontrib>Ertürk, Ä°smail</creatorcontrib><creatorcontrib>Demir, Hacer</creatorcontrib><creatorcontrib>Aslan, Ferit</creatorcontrib><creatorcontrib>Sönmez, üzlem</creatorcontrib><creatorcontrib>Korkmaz, Taner</creatorcontrib><creatorcontrib>Celayir, üzde Melisa</creatorcontrib><creatorcontrib>KaradaÄ, Ä°brahim</creatorcontrib><creatorcontrib>KayikçioÄlu, Erkan</creatorcontrib><creatorcontrib>Åakalar, Teoman</creatorcontrib><creatorcontrib>üktem, Ä°lker Nihat</creatorcontrib><creatorcontrib>Eren, Tülay</creatorcontrib><creatorcontrib>Urul, Enes</creatorcontrib><creatorcontrib>Mocan, Eda Eylemer</creatorcontrib><creatorcontrib>Kalkan, Ziya</creatorcontrib><creatorcontrib>Yildirim, Nilgün</creatorcontrib><creatorcontrib>Ergün, Yakup</creatorcontrib><creatorcontrib>Akagündüz, Baran</creatorcontrib><creatorcontrib>Karakaya, Serdar</creatorcontrib><creatorcontrib>Kut, Engin</creatorcontrib><creatorcontrib>Teker, Fatih</creatorcontrib><creatorcontrib>Demirel, Burçin Çakan</creatorcontrib><creatorcontrib>Karaboyun, Kubilay</creatorcontrib><creatorcontrib>Almuradova, Elvina</creatorcontrib><creatorcontrib>Ãnal, Olçun Ãmit</creatorcontrib><creatorcontrib>Oyman, Abdilkerim</creatorcontrib><creatorcontrib>IÅik, Deniz</creatorcontrib><creatorcontrib>Okutur, Kerem</creatorcontrib><creatorcontrib>üztosun, BuÄra</creatorcontrib><creatorcontrib>GülbaÄci, Burcu Belen</creatorcontrib><creatorcontrib>Kalender, Mehmet Emin</creatorcontrib><creatorcontrib>Åahin, Elif</creatorcontrib><creatorcontrib>Seyyar, Mustafa</creatorcontrib><creatorcontrib>üzdemir, üzlem</creatorcontrib><creatorcontrib>Selçukbiricik, Fatih</creatorcontrib><creatorcontrib>Kanitez, Metin</creatorcontrib><creatorcontrib>Dede, Ä°sa</creatorcontrib><creatorcontrib>GümüÅ, Mahmut</creatorcontrib><creatorcontrib>Gökmen, Erhan</creatorcontrib><creatorcontrib>Yaren, Arzu</creatorcontrib><creatorcontrib>MenekÅe, Serkan</creatorcontrib><creatorcontrib>Ebinç, Senar</creatorcontrib><creatorcontrib>Aksoy, Sercan</creatorcontrib><creatorcontrib>Ä°mamoÄlu, GökÅen Ä°nanç</creatorcontrib><creatorcontrib>AltinbaÅ, Mustafa</creatorcontrib><creatorcontrib>Çetin, Bülent</creatorcontrib><creatorcontrib>Uluç, BaÅak Oyan</creatorcontrib><creatorcontrib>Er, üzlem</creatorcontrib><creatorcontrib>KaradurmuÅ, Nuri</creatorcontrib><creatorcontrib>ErdoÄan, Atike Pinar</creatorcontrib><creatorcontrib>Artaç, Mehmet</creatorcontrib><creatorcontrib>Tanriverdi, üzgür</creatorcontrib><creatorcontrib>Çiçin, Ä°rfan</creatorcontrib><creatorcontrib>Åendur, Mehmet Ali Nahit</creatorcontrib><creatorcontrib>Oktay, Esin</creatorcontrib><creatorcontrib>BayoÄlu, Ä°brahim Vedat</creatorcontrib><creatorcontrib>PaydaÅ, Semra</creatorcontrib><creatorcontrib>Aydiner, Adnan</creatorcontrib><creatorcontrib>Salim, Derya Kivrak</creatorcontrib><creatorcontrib>Geredeli, ÇaÄlayan</creatorcontrib><creatorcontrib>YavuzÅen, TuÄba</creatorcontrib><creatorcontrib>DoÄan, Mutlu</creatorcontrib><creatorcontrib>HacibekiroÄlu, Ä°lhan</creatorcontrib><title>Efficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy</title><title>BMC Cancer</title><description>Background There is no standard treatment recommended at category 1 level in international guidelines for subsequent therapy after cyclin-dependent kinase 4/6 inhibitor (CDK4/6) based therapy. We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression under CDKi. In addition, we aimed to show the effectiveness of systemic treatments after CDKi and whether there is a survival difference between hormonal treatments (monotherapy vs. mTOR-based). Methods A total of 609 patients from 53 centers were included in the study. Progression-free-survivals (PFS) of subsequent treatments (chemotherapy (CT, n:434) or endocrine therapy (ET, n:175)) after CDKi were calculated. Patients were evaluated in three groups as those who received CDKi in first-line (group A, n:202), second-line (group B, n: 153) and [greater than or equal to] 3rd-line (group C, n: 254). PFS was compared according to the use of ET and CT. In addition, ET was compared as monotherapy versus everolimus-based combination therapy. Results The median duration of CDKi in the ET arms of Group A, B, and C was 17.0, 11.0, and 8.5 months in respectively; it was 9.0, 7.0, and 5.0 months in the CT arm. Median PFS after CDKi was 9.5 (5.0-14.0) months in the ET arm of group A, and 5.3 (3.9-6.8) months in the CT arm (p = 0.073). It was 6.7 (5.8-7.7) months in the ET arm of group B, and 5.7 (4.6-6.7) months in the CT arm (p = 0.311). It was 5.3 (2.5-8.0) months in the ET arm of group C and 4.0 (3.5-4.6) months in the CT arm (p = 0.434). Patients who received ET after CDKi were compared as those who received everolimus-based combination therapy versus those who received monotherapy ET: the median PFS in group A, B, and C was 11.0 vs. 5.9 (p = 0.047), 6.7 vs. 5.0 (p = 0.164), 6.7 vs. 3.9 (p = 0.763) months. Conclusion Physicians preferred CT rather than ET in patients with early progression under CDKi. It has been shown that subsequent ET after CDKi can be as effective as CT. It was also observed that better PFS could be achieved with the subsequent everolimus-based treatments after first-line CDKi compared to monotherapy ET. Keywords: Advanced breast cancer, Cyclin-dependent kinase, Ribociclib, Palbociclib, Everolimus, Fulvestrant, Endocrine treatment, Hormonotherapy</description><subject>Analysis</subject><subject>Antimitotic agents</subject><subject>Antineoplastic agents</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Cyclins</subject><subject>Development and progression</subject><subject>Dosage and administration</subject><subject>Hormone therapy</subject><subject>Patient outcomes</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2023</creationdate><recordtype>report</recordtype><sourceid/><recordid>eNqVjs1OwzAQhC0EEuXnBTjtC7i1k5CYIypFSL1yR05s14saO3idVn0RnheDOHDlNN-MdrTD2J0USylVuyJZKXXPRVVzKVrxwNUZW8imk7xqRHf-hy_ZFdG7ELJTQi3Y58Y5HPRwguiA5p7sx2xDhpyszmMhAgww6Yw_fMTswcc0xmD5FAkzHixoc9BhsAb60qIMw7dLcPQRvDZgkEpsYUpxlywRxgBzMOVi_bSFZtWWFx57zDFB9jbp6XTDLpzek7391Wu2fN68rl_4Tu_tGwYXc9JltjZ2xKGMcVjyx65u27rqmqb-d-ELIhVoZQ</recordid><startdate>20230210</startdate><enddate>20230210</enddate><creator>Karacin, Cengiz</creator><creator>Oksuzoglu, Berna</creator><creator>Demirci, AyÅe</creator><creator>Keskinkiliç, Merve</creator><creator>Baytemür, Naziyet Köse</creator><creator>Yilmaz, Funda</creator><creator>Selvi, OÄuzhan</creator><creator>Erdem, Dilek</creator><creator>AvÅar, Esin</creator><creator>Paksoy, Nail</creator><creator>Demir, Necla</creator><creator>Göksu, Sema 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Hacer</au><au>Aslan, Ferit</au><au>Sönmez, üzlem</au><au>Korkmaz, Taner</au><au>Celayir, üzde Melisa</au><au>KaradaÄ, Ä°brahim</au><au>KayikçioÄlu, Erkan</au><au>Åakalar, Teoman</au><au>üktem, Ä°lker Nihat</au><au>Eren, Tülay</au><au>Urul, Enes</au><au>Mocan, Eda Eylemer</au><au>Kalkan, Ziya</au><au>Yildirim, Nilgün</au><au>Ergün, Yakup</au><au>Akagündüz, Baran</au><au>Karakaya, Serdar</au><au>Kut, Engin</au><au>Teker, Fatih</au><au>Demirel, Burçin Çakan</au><au>Karaboyun, Kubilay</au><au>Almuradova, Elvina</au><au>Ãnal, Olçun Ãmit</au><au>Oyman, Abdilkerim</au><au>IÅik, Deniz</au><au>Okutur, Kerem</au><au>üztosun, BuÄra</au><au>GülbaÄci, Burcu Belen</au><au>Kalender, Mehmet Emin</au><au>Åahin, Elif</au><au>Seyyar, Mustafa</au><au>üzdemir, üzlem</au><au>Selçukbiricik, Fatih</au><au>Kanitez, Metin</au><au>Dede, Ä°sa</au><au>GümüÅ, Mahmut</au><au>Gökmen, Erhan</au><au>Yaren, Arzu</au><au>MenekÅe, Serkan</au><au>Ebinç, Senar</au><au>Aksoy, Sercan</au><au>Ä°mamoÄlu, GökÅen Ä°nanç</au><au>AltinbaÅ, Mustafa</au><au>Çetin, Bülent</au><au>Uluç, BaÅak Oyan</au><au>Er, üzlem</au><au>KaradurmuÅ, Nuri</au><au>ErdoÄan, Atike Pinar</au><au>Artaç, Mehmet</au><au>Tanriverdi, üzgür</au><au>Çiçin, Ä°rfan</au><au>Åendur, Mehmet Ali Nahit</au><au>Oktay, Esin</au><au>BayoÄlu, Ä°brahim Vedat</au><au>PaydaÅ, Semra</au><au>Aydiner, Adnan</au><au>Salim, Derya Kivrak</au><au>Geredeli, ÇaÄlayan</au><au>YavuzÅen, TuÄba</au><au>DoÄan, Mutlu</au><au>HacibekiroÄlu, Ä°lhan</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Efficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy</atitle><jtitle>BMC Cancer</jtitle><date>2023-02-10</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>Background There is no standard treatment recommended at category 1 level in international guidelines for subsequent therapy after cyclin-dependent kinase 4/6 inhibitor (CDK4/6) based therapy. We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression under CDKi. In addition, we aimed to show the effectiveness of systemic treatments after CDKi and whether there is a survival difference between hormonal treatments (monotherapy vs. mTOR-based). Methods A total of 609 patients from 53 centers were included in the study. Progression-free-survivals (PFS) of subsequent treatments (chemotherapy (CT, n:434) or endocrine therapy (ET, n:175)) after CDKi were calculated. Patients were evaluated in three groups as those who received CDKi in first-line (group A, n:202), second-line (group B, n: 153) and [greater than or equal to] 3rd-line (group C, n: 254). PFS was compared according to the use of ET and CT. In addition, ET was compared as monotherapy versus everolimus-based combination therapy. Results The median duration of CDKi in the ET arms of Group A, B, and C was 17.0, 11.0, and 8.5 months in respectively; it was 9.0, 7.0, and 5.0 months in the CT arm. Median PFS after CDKi was 9.5 (5.0-14.0) months in the ET arm of group A, and 5.3 (3.9-6.8) months in the CT arm (p = 0.073). It was 6.7 (5.8-7.7) months in the ET arm of group B, and 5.7 (4.6-6.7) months in the CT arm (p = 0.311). It was 5.3 (2.5-8.0) months in the ET arm of group C and 4.0 (3.5-4.6) months in the CT arm (p = 0.434). Patients who received ET after CDKi were compared as those who received everolimus-based combination therapy versus those who received monotherapy ET: the median PFS in group A, B, and C was 11.0 vs. 5.9 (p = 0.047), 6.7 vs. 5.0 (p = 0.164), 6.7 vs. 3.9 (p = 0.763) months. Conclusion Physicians preferred CT rather than ET in patients with early progression under CDKi. It has been shown that subsequent ET after CDKi can be as effective as CT. It was also observed that better PFS could be achieved with the subsequent everolimus-based treatments after first-line CDKi compared to monotherapy ET. Keywords: Advanced breast cancer, Cyclin-dependent kinase, Ribociclib, Palbociclib, Everolimus, Fulvestrant, Endocrine treatment, Hormonotherapy</abstract><pub>BioMed Central Ltd</pub><doi>10.1186/s12885-023-10609-8</doi></addata></record>
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source Publicly Available Content Database; PubMed Central
subjects Analysis
Antimitotic agents
Antineoplastic agents
Breast cancer
Cancer
Care and treatment
Chemotherapy
Cyclins
Development and progression
Dosage and administration
Hormone therapy
Patient outcomes
title Efficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy
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