Real-World Experience among Elderly Metastatic Breast Cancer Patients Treated with CDK4/6 Inhibitor-Based Therapy

被引:2
|
作者
O'Connor, Thomas N. [1 ]
Schultz, Emily [1 ]
Wang, Jianxin [1 ]
O'Connor, Tracey [2 ]
Levine, Ellis [2 ]
Knudsen, Erik S. [1 ]
Witkiewicz, Agnieszka K. [1 ,3 ]
机构
[1] Roswell Pk Comprehens Canc Ctr, Dept Mol & Cellular Biol, Buffalo, NY 14263 USA
[2] Roswell Pk Comprehens Canc Ctr, Dept Med, Buffalo, NY 14263 USA
[3] Roswell Pk Comprehens Canc Ctr, Dept Pathol, Buffalo, NY 14263 USA
关键词
breast cancer; elderly; CDK4/6; inhibitor; metastatic; RIBOCICLIB PLUS LETROZOLE; ENDOCRINE THERAPY; OLDER PATIENTS; DRUG REGISTRATION; CLINICAL-TRIALS; OPEN-LABEL; PALBOCICLIB; WOMEN; COMBINATION; MULTICENTER;
D O I
10.3390/cancers16091749
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The largest portion of breast cancer patients diagnosed after 70 years of age present with hormone receptor-positive (HR+) breast cancer subtypes. Cyclin-dependent kinase (CDK) 4/6 inhibitor treatment, in conjunction with endocrine therapy, has become standard-of-care for metastatic HR+ breast cancer. In total, 320 patients with metastatic breast cancer receiving CDK4/6 inhibitor combined with fulvestrant or an aromatase inhibitor were enrolled in an ongoing observational study or were included in an IRB-approved retrospective study. All patients receiving CDK4/6 inhibitor-based therapy that were >= 70 years of age (n = 111) displayed prolonged progression-free survival (27.6 months) as compared to patients <70 years of age (n = 209, 21.1 months, HR = 1.38, p < 0.05). Specifically, patients receiving a CDK4/6 inhibitor with an aromatase inhibitor who were >= 70 years of age (n = 79) displayed exceptionally prolonged progression-free survival (46.0 months) as compared to patients receiving the same treatment who were <70 years of age (n = 161, 21.8 months, HR = 1.71, p < 0.01). However, patients >= 70 years of age also experienced more frequent adverse responses to CDK4/6 inhibitor-based treatment leading to dose reduction, hold, or discontinuation than the younger cohort (69% and 53%, respectively). Treatment strategies that may decrease toxicity without affecting efficacy (such as dose titration) are worth further exploration.
引用
收藏
页数:12
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