Long-term efficacy analysis of the randomised, phase II TRYPHAENA cardiac safety study: Evaluating pertuzumab and trastuzumab plus standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer

被引:181
作者
Schneeweiss, Andreas [1 ]
Chia, Stephen [2 ]
Hickish, Tamas [3 ]
Harvey, Vernon [4 ]
Eniu, Alexandru [5 ]
Waldron-Lynch, Maeve [6 ]
Eng-Wong, Jennifer [7 ]
Kirk, Sarah [8 ]
Cortes, Javier [9 ,10 ]
机构
[1] Univ Hosp, Natl Ctr Tumor Dis, Neuenheimer Feld 460, D-69120 Heidelberg, Germany
[2] Univ British Columbia, British Columbia Canc Agcy, Vancouver Ctr, Vancouver, BC, Canada
[3] Bournemouth Univ, Royal Bournemouth Hosp, Bournemouth, Dorset, England
[4] Auckland City Hosp, Reg Canc & Blood Serv, Auckland, New Zealand
[5] Canc Inst Ion Chiricuta, Cluj Napoca, Romania
[6] Roche Prod Ltd, Global Prod Dev, Clin Sci, Welwyn Garden City, Herts, England
[7] Genentech Inc, Prod Dev Oncol, San Francisco, CA 94080 USA
[8] Roche Prod Ltd, PDBB Biostat, Welwyn Garden City, Herts, England
[9] Ramon y Cajal Univ Hosp, Madrid, Spain
[10] Vall dHebron Inst Oncol VHIO, Barcelona, Spain
关键词
Neoadjuvant therapy; Pertuzumab; Trastuzumab; Breast cancer; Safety; Cardiotoxicity; Clinical efficacy; Disease-free survival; PATHOLOGICAL COMPLETE RESPONSE; ADJUVANT TRASTUZUMAB; OPEN-LABEL; FOLLOW-UP; CLINICAL-TRIALS; SURVIVAL; MULTICENTER; THERAPY; ASSOCIATION; DOCETAXEL;
D O I
10.1016/j.ejca.2017.10.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We report long-term efficacy and cardiac safety outcomes in patients with HER2-positive early breast cancer treated with neoadjuvant pertuzumab plus trastuzumab with anthracycline-containing or anthracycline-free chemotherapy. Methods: Descriptive efficacy analyses were conducted in patients randomised to group A ( cycles 1-6: trastuzumab [8 mg/kg loading dose and 6 mg/kg maintenance] plus pertuzumab [840 mg loading dose and 420 mg maintenance], plus 5-fluorouracil, epirubicin and cyclophosphamide [FEC] [cycles 1-3; 500 mg/m 2 5-fluorouracil/100 mg/m(2) epirubicin/600 mg/m(2) cyclophosphamide] then docetaxel [cycles 4-6; 75 mg/m(2), escalated to 100 mg/m(2) if well tolerated]), B (cycles 1-3: FEC, cycles 4-6: trastuzumab plus pertuzumab plus docetaxel as mentioned previously) or C (cycles 1-6: trastuzumab plus pertuzumab plus docetaxel [75 mg/m(2), without dose escalation], and carboplatin [AUC 6]), five years after randomisation of the last patient. This study is registered with ClinicalTrials. gov, number NCT00976989. Results: Three-year KaplaneMeier survival estimates for disease-free survival (DFS) were 87% (95% confidence interval: 79-95), 88% (80-96) and 90% (82-97) in groups AeC, respectively. Progression-free survival (PFS) rates were 89% (81-96), 89% (81-96) and 87% (80-95). DFS hazard ratio for total pathological complete response (tpCR) versus no tpCR was 0.27 (0.11-0.64). During post-treatment follow-up, 2/72 (2.8%), 3/75 (4.0%) and 4/76 (5.4%) patients in groups AeC had any-grade left ventricular systolic dysfunction; eight (11.1%), 12 (16.0%) and nine (11.8%) patients experienced left ventricular ejection fraction declines >= 10% from baseline to <50%. Conclusions: Long-term DFS and PFS were similar between groups. Patients who achieved tpCR had improved DFS. No new safety signals were identified. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:27 / 35
页数:9
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