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Impact of cyclin dependent kinase 4/6 inhibitors on breast cancer brain metastasis outcomes.
Chew, Sonya M; Ferraro, Emanuela; Safonov, Anton; Chen, Yuan; Kelly, Daniel; Razavi, Pedram; Robson, Mark; Seidman, Andrew D.
  • Chew SM; Medical Oncology Service, University Hospital Galway, Galway, Ireland.
  • Ferraro E; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Safonov A; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Chen Y; Epidemiology-Biostatistics Service, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Kelly D; Technology Division, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Razavi P; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA; Department of Medicine, Weill Cornell Medical College, New York, USA.
  • Robson M; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA; Department of Medicine, Weill Cornell Medical College, New York, USA.
  • Seidman AD; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, USA; Department of Medicine, Weill Cornell Medical College, New York, USA. Electronic address: seidmana@mskcc.org.
Eur J Cancer ; 207: 114175, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38896996
ABSTRACT

BACKGROUND:

Cyclin dependent kinase 4/6 inhibitors (CDK4/6i) are recommended 1st line treatments in HR+HER2- metastatic breast cancer. However, the impact of prior CDK4/6i on the natural history of brain metastases (BM) is not well described. MATERIALS AND

METHODS:

We reviewed retrospective data for 363 patients with HR+HER2- BM who received a CDK4/6i (CDK-Y) between 1 Jan 2015 to 31 July 2021 and 299 patients with HR+HER2- BM who did not receive a CDK4/6i (CDK-N) between 1 Jan 2010 to 31 Dec 2014. CNS PFS and OS were assessed in patients who received CDK4/6i after BM. OS from the time of BM development was assessed between patients who received CDK4/6i before BM and the CDK-N cohort

RESULTS:

In the CDK-Y cohort of 363 patients, 203 (56 %) received a CDK4/6i before BM, 133 (37 %) received a CDK4/6i only after BM and 27 (7 %) received a CDK4/6i both before and after BM. Median CNS PFS was 21.4 months for patients receiving a CDK4/6i only after BM and 9.4 months for patients who received CDK4/6i both before and after BM (p = 0.006). Median OS was 24.9 months for patients receiving a CDK4/6i only after BM and 12.1 months for patients who received CDK4/6i both before and after BM (p = 0.0098). Median OS from time of BM development for patients receiving a CDK4/6i before BM versus the CDK-N cohort was 4.3 months and 7.7 months respectively (p = 0.0082).

CONCLUSIONS:

CDK4/6i exposure prior to BM may lead to development of resistance mechanisms which in turn reduces CNS PFS and OS upon rechallenging with a CDK4/6i after BM development. This motivates investigation of biomarkers for patient selection.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Neoplasias de la Mama / Inhibidores de Proteínas Quinasas / Quinasa 4 Dependiente de la Ciclina / Quinasa 6 Dependiente de la Ciclina Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Neoplasias de la Mama / Inhibidores de Proteínas Quinasas / Quinasa 4 Dependiente de la Ciclina / Quinasa 6 Dependiente de la Ciclina Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Año: 2024 Tipo del documento: Article