Al-Foheidi Meteb H, Albeshri Asem Mohammed, Moamenkahan Safwan Noor, Abdullah Abdulmajid Mohammed, Abualola Muhannad Sadaqa, Alharbi Muath Hamed, Refa Ahmed A, Bayer Ali M, Shaheen Ahmed Y, Aga Syed Sameer, Khan Muhammad Anwar, Al-Mansour Mubarak M, Ibrahim Ezzeldin M
Princess Noorah Oncology Center, National Guard Health Affairs, King Saud Bin Abdul Aziz University for Health Sciences, King Abdullah International Medical Research Center, King Abdulaziz Medical City, Jeddah 21423, Kingdom of Saudi Arabia.
Oncology Center, International Medical Center, King Saud Bin Abdul Aziz University for Health Sciences, King Abdullah International Medical Research Center, King Abdulaziz Medical City, Jeddah 21423, Kingdom of Saudi Arabia.
Mol Clin Oncol. 2022 Jun 1;17(1):119. doi: 10.3892/mco.2022.2552. eCollection 2022 Jul.
The addition of palbociclib (a cyclin-dependent kinase 4/6 inhibitor) to endocrine therapy (ET) has been shown to significantly improve progression-free survival (PFS) and overall survival (OS) among patients with hormone receptor-positive (HR) advanced breast cancer. The current study presents the local experience of using palbociclib at two cancer centers in Saudi Arabia. Electronic data of patients with metastatic HR and human epidermal growth factor receptor 2-negative breast cancer who progressed after prior ET and received at least one cycle of palbociclib plus ET, were retrospectively reviewed. A total of 97 patients were identified, and their data were included in the analysis. The median age of the patients was 55 years. Patients were heavily pretreated in the metastatic setting (55% received systemic chemotherapy and 49% received two or more lines of prior ET). In total, 29 (30%) and 50 (52%) patients achieved an objective response and clinical benefit, respectively. The median follow-up time was 31.0 months [95% confidence interval (CI), 16.9-44.9] and the median PFS time was 16.3 months (95% CI, 11.4-21.2), with 58% of patients remaining progression-free at 12 months. Upon multivariate regression analysis, liver involvement was the only significant independent variable that predicted a greater risk of progression or death (hazard ratio, 2.32; 95% CI, 1.22-4.40; P=0.010). The median OS time was 19.6 months (95% CI, 18.1-20.9), with 12- and 24-month OS rates of 75 and 30%, respectively. Overall, real-world data showed that administration of palbociclib in combination with ET in patients with advanced HR breast cancer achieved a favorable outcome that was comparable to that reported in clinical trials.
在激素受体阳性(HR)的晚期乳腺癌患者中,将哌柏西利(一种细胞周期蛋白依赖性激酶4/6抑制剂)添加到内分泌治疗(ET)中已被证明可显著改善无进展生存期(PFS)和总生存期(OS)。本研究展示了沙特阿拉伯两个癌症中心使用哌柏西利的本地经验。对转移性HR和人表皮生长因子受体2阴性乳腺癌患者的电子数据进行了回顾性分析,这些患者在先前的ET治疗后病情进展,并接受了至少一个周期的哌柏西利加ET治疗。共确定了97例患者,并将其数据纳入分析。患者的中位年龄为55岁。患者在转移性疾病阶段接受了大量前期治疗(55%接受过全身化疗,49%接受过两线或更多线的前期ET治疗)。总共有29例(30%)和50例(52%)患者分别实现了客观缓解和临床获益。中位随访时间为31.0个月[95%置信区间(CI),16.9 - 44.9],中位PFS时间为16.3个月(95% CI,11.4 - 21.2),58%的患者在12个月时仍无进展。多因素回归分析显示,肝脏受累是唯一显著的独立变量,可预测更高的进展或死亡风险(风险比,2.32;95% CI,1.22 - 4.40;P = 0.010)。中位OS时间为19.6个月(95% CI,18.1 - 20.9),12个月和24个月的OS率分别为75%和30%。总体而言,真实世界数据表明,在晚期HR乳腺癌患者中,将哌柏西利与ET联合使用可取得与临床试验报告相当的良好结果。