Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, and Department of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Clin Cancer Res. 2015 Oct 1;21(19):4365-72. doi: 10.1158/1078-0432.CCR-14-3354. Epub 2015 May 15.
The association between PIK3CA mutations and response to neoadjuvant chemotherapy in women with primary breast cancer is not fully elucidated.
PIK3CA mutations in breast cancer tissues that were taken prior to the initiation of neoadjuvant chemotherapy were identified in 729 operable primary breast cancer patients who received neoadjuvant chemotherapy. Among these, the PIK3CA mutations were also reassessed in tumor tissues procured following operation in 102 patients after completion of neoadjuvant chemotherapy.
A total of 206 out of 729 (28.3%) patients had PIK3CA mutations, and 19.5% of patients (142/729) in this cohort achieved a pathologic complete response (pCR) after neoadjuvant chemotherapy. Patients with PIK3CA mutations exhibited a lower pCR rate than did those with wild-type (14.6% vs. 21.4%, P = 0.035). No significant differences in disease-free survival (DFS) or distant disease-free survival (DDFS) were observed between PIK3CA mutant and wild-type in the entire study population. Among the 102 patients with PIK3CA mutation statuses available before and after neoadjuvant chemotherapy, 24 patients (23.5%) had PIK3CA mutations before neoadjuvant chemotherapy. Of these 24 patients, 15 patients retained their initial PIK3CA mutations and 9 patients lost their initial mutations after neoadjuvant chemotherapy. Patients who retained the initial mutations after neoadjuvant chemotherapy (n = 15) had a worse DDFS than the remaining patients (n = 87) in this subgroup [unadjusted HR, 2.34; 95% confidence interval (CI), 0.98-5.62; P = 0.050].
Patients with PIK3CA mutations are less likely to respond to neoadjuvant chemotherapy. Patients who retain their initial PIK3CA mutations after neoadjuvant chemotherapy have an unfavorable survival.
PIK3CA 突变与原发性乳腺癌患者新辅助化疗反应之间的关系尚未完全阐明。
在 729 例接受新辅助化疗的可手术原发性乳腺癌患者中,检测了新辅助化疗前采集的乳腺癌组织中的 PIK3CA 突变。其中,在 102 例新辅助化疗完成后手术切除的肿瘤组织中,对 PIK3CA 突变也进行了重新评估。
729 例患者中共有 206 例(28.3%)存在 PIK3CA 突变,该队列中有 19.5%(142/729)的患者在新辅助化疗后获得了病理完全缓解(pCR)。携带 PIK3CA 突变的患者 pCR 率低于野生型患者(14.6%比 21.4%,P=0.035)。在整个研究人群中,PIK3CA 突变型和野生型患者的无病生存率(DFS)或远处无病生存率(DDFS)无显著差异。在新辅助化疗前后可获得 PIK3CA 突变状态的 102 例患者中,24 例(23.5%)患者在新辅助化疗前存在 PIK3CA 突变。在这 24 例患者中,15 例患者保留了初始 PIK3CA 突变,9 例患者在新辅助化疗后丢失了初始突变。在新辅助化疗后保留初始突变的患者(n=15)与亚组中其余患者(n=87)的 DDFS 更差[未调整的 HR,2.34;95%置信区间(CI),0.98-5.62;P=0.050]。
存在 PIK3CA 突变的患者对新辅助化疗的反应性较低。新辅助化疗后保留初始 PIK3CA 突变的患者生存状况较差。