Neoadjuvant carboplatin in triple-negative breast cancer: results from NACATRINE, a randomized phase II clinical trial

被引:2
|
作者
Souza, Cristiano de Padua [1 ]
Carneiro, Ana Suellen Barroso [1 ]
Lessa, Ana Cecilia de Oliveira [1 ]
Lacerda, Domicio Carvalho [1 ]
Paiva, Carlos Eduardo [1 ]
Zorzetto, Marina Moreira Costa [1 ]
de Freitas, Ana Julia Aguiar [2 ]
Santana, Iara Viana Vidigal [3 ]
de Oliveira, Marco Antonio [4 ]
Palmero, Edenir Inez [2 ,5 ]
Marques, Marcia Maria Chiquitelli [2 ]
Reinert, Tomas [6 ,7 ]
机构
[1] Barretos Canc Hosp, Barretos, SP, Brazil
[2] Barretos Canc Hosp, Teaching & Res Inst, Mol Oncol Res Ctr, Barretos, SP, Brazil
[3] Barretos Canc Hosp, Pathol Dept, Barretos, SP, Brazil
[4] Barretos Canc Hosp, Nucleus Epidemiol & Biostat, Barretos, SP, Brazil
[5] Brazilian Natl Canc Inst, Dept Genet, Rio De Janeiro, Brazil
[6] Oncoclinicas, Porto Alegre, Brazil
[7] Grp Brasileiro Estudos Canc Mama GBECAM, Porto Alegre, Brazil
关键词
Breast neoplasm; Neoadjuvant chemotherapy; Triple-negative breast cancer; BRCA; CHEMOTHERAPY; BRIGHTNESS; VELIPARIB; IMPACT;
D O I
10.1007/s10549-023-07011-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundNeoadjuvant chemotherapy (NACT) is the mainstay of treatment of stages II and III triple-negative breast cancer (TNBC). This study aims to evaluate if the addition of carboplatin to NACT is associated with an increase in the pathological complete response (pCR) rates in TNBC.MethodsWe conducted an open-label phase II randomized clinical trial in a single center in Brazil. Patients with stage II and III TNBC were randomized to receive standard NACT with or without carboplatin. All the patients received doxorubicin (60 mg/m(2)) plus cyclophosphamide (600 mg/m(2)) both intravenously (i.v.) q21 days for four cycles. Patients were then randomized for additional treatment with weekly (wk) paclitaxel (80 mg/m(2) i.v., for 12 cycles) plus wk carboplatin AUC 1.5 (experimental arm) or without wk carboplatin (control arm). Randomization was stratified according to gBRCA status, age, and AJCC 8th edition clinical stage (II vs. III). The primary endpoint was the pathologic complete response (pCR) rate. Secondary endpoints included recurrence-free survival and overall survival.ResultsBetween 2017 and 2021, 146 patients were randomized, 73 on each arm. The median age was 45 years. Most patients (66.4%) had locally advanced stage III disease, 67.1% had T3/T4 tumors, and 56.2% had clinically positive axillary lymph nodes. Germline BRCA status was available for all patients, and 19.9% had pathogenic BRCA1/2 variants. The pCR rate (ypT0ypN0) was numerically increased by 13.7%, being 43.8% (31 of 73 patients) in the experimental and 30.1% (22 of 73 patients) in the control arm, not meeting the prespecified goal of increasing the pCR in 15% (p-value = 0.08). Survival outcomes are immature.ConclusionThe addition of carboplatin to standard NACT in stages II and III TNBC was associated with a non-statistically significant numerical increase in the pCR rate. Follow-up for survival outcomes and translational research initiatives are ongoing.
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收藏
页码:57 / 65
页数:9
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