Neoadjuvant checkpoint blockade in combination with Chemotherapy in patients with tripe-negative breast cancer: exploratory analysis of real-world, multicenter data

被引:10
作者
Deng, Heran [1 ]
Wang, Liying [1 ]
Wang, Na [2 ]
Zhang, Kejin [3 ]
Zhao, Yanxia [4 ]
Qiu, Pengfei [5 ]
Qi, Xiaowei [6 ]
Zhang, Danhua [7 ]
Xu, Fei [2 ]
Liu, Jieqiong [1 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Breast Tumor Ctr, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Yanjiang West Rd 107, Guangzhou 510120, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Univ Canc Ctr, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Dongfeng Rd 651, Guangzhou 510060, Guangdong, Peoples R China
[3] Cent South Univ, Ctr South Univ, Xiangya Hosp, Changsha, Hunan, Peoples R China
[4] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Wuhan, Hubei, Peoples R China
[5] Shandong Univ, Shandong Tumor Hosp, Jinan, Shandong, Peoples R China
[6] Army Med Univ, Southwest Hosp AMU, Chongqing, Sichuan, Peoples R China
[7] Cent South Univ, Ctr South Univ, Xiangya Hosp 2, Changsha, Hunan, Peoples R China
关键词
Tripe-negative breast cancer; Neoadjuvant immunotherapy; Anti-PD-1; L1; antibody; Real-world study; PEMBROLIZUMAB PLUS CHEMOTHERAPY; ADVERSE EVENTS; SURVIVAL;
D O I
10.1186/s12885-023-10515-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Despite the poor prognosis of triple-negative breast cancer (TNBC), it has been demonstrated that neoadjuvant immunotherapy in combination with chemotherapy can improve the pathologic complete response (pCR) rate and/or long-term outcome of TNBC. However, there have been no real-world studies reporting on the effectiveness of neoadjuvant checkpoint inhibitors in early TNBC.Methods Between November 2019 and December 2021, 63 early TNBC patients treated with anti-PD-1 antibodies (pembrolizumab or camrelizumab) or anti-PD-L1 antibody (atezolizumab) in combination with chemotherapy at seven institutions were included. PCR1 defined as ypT0/Tis and ypN0 was the primary endpoint. Secondary endpoints included pCR2 defined as ypT0/Tis, overall response rate (ORR), disease-free survival (DFS), drug-related adverse events (AEs) and biomarkers.ResultsAmong the patients in the current study, 34.9% of patients were able to achieve pCR1, and 47.6% of patients had achieved pCR2. The ORR was 82.5%. 33 patients with non-pCR2 tumors were found to have a median DFS of 20.7 months (95% CI 16.3 months-not reached). The DFS of patients with pCR2 and non-pCR2 after neoadjuvant therapy was significantly different (HR = 0.28, 95% CI 0.10-0.79; P = 0.038). The most common AEs were nausea (63.4%), fatigue (42.7%), leucopenia (30.0%) and elevated transaminase (11.7%).Conclusion It is possible to achieve a meaningful pCR rate and DFS by combining neoadjuvant checkpoint blockade with chemotherapy in patients with high-risk TNBC. Compared to clinical trials, however, there was a slightly lower pCR rate in this multicentered real-world study.
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页数:9
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