Literature DB >> 25979484

Association of PIK3CA Mutation Status before and after Neoadjuvant Chemotherapy with Response to Chemotherapy in Women with Breast Cancer.

Hua Yuan1, Jiuan Chen1, Yiqiang Liu1, Tao Ouyang1, Jinfeng Li1, Tianfeng Wang1, Zhaoqing Fan1, Tie Fan1, Benyao Lin1, Yuntao Xie2.   

Abstract

PURPOSE: The association between PIK3CA mutations and response to neoadjuvant chemotherapy in women with primary breast cancer is not fully elucidated. EXPERIMENTAL
DESIGN: 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.
RESULTS: 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].
CONCLUSIONS: 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. ©2015 American Association for Cancer Research.

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Year:  2015        PMID: 25979484     DOI: 10.1158/1078-0432.CCR-14-3354

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  17 in total

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2.  Low expression of RECQL is associated with poor prognosis in Chinese breast cancer patients.

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Review 6.  PIK3CA mutations and their response to neoadjuvant treatment in early breast cancer: A systematic review and meta-analysis.

Authors:  Hongwei Fan; Chao Li; Qian Xiang; Ling Xu; Zhuo Zhang; Qianxin Liu; Tonttong Zhang; Ying Zhou; Xia Zhao; Yimin Cui
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7.  Somatic alterations of TP53, ERBB2, PIK3CA and CCND1 are associated with chemosensitivity for breast cancers.

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Journal:  Cancer Sci       Date:  2019-03-19       Impact factor: 6.716

8.  PI3K activation promotes resistance to eribulin in HER2-negative breast cancer.

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Journal:  Br J Cancer       Date:  2021-03-15       Impact factor: 7.640

9.  Prevalence and Prognostic Role of PIK3CA/AKT1 Mutations in Chinese Breast Cancer Patients.

Authors:  Ling Deng; Xuehua Zhu; Yun Sun; Jiemin Wang; Xiaorong Zhong; Jiayuan Li; Min Hu; Hong Zheng
Journal:  Cancer Res Treat       Date:  2018-03-15       Impact factor: 4.679

10.  PIK3CA Mutations and Neoadjuvant Therapy Outcome in Patients with Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer: A Sequential Analysis.

Authors:  Youjeong Seo; Yeon Hee Park; Jin Seok Ahn; Young-Hyuck Im; Seok Jin Nam; Soo Youn Cho; Eun Yoon Cho
Journal:  J Breast Cancer       Date:  2018-10-29       Impact factor: 3.588

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