Long-term outcomes of neoadjuvant trastuzumab emtansine plus pertuzumab (T-DM1+P) and docetaxel plus carboplatin plus trastuzumab plus pertuzumab (TCbHP) for HER2-positive primary breast cancer: results of the randomized phase 2 JBCRG20 study (Neo-peaks)

被引:2
|
作者
Takano, Toshimi [1 ]
Masuda, Norikazu [2 ,20 ]
Ito, Mitsuya [3 ]
Inoue, Kenichi [4 ]
Tanabe, Yuko [5 ]
Kawaguchi, Kousuke [6 ]
Yasojima, Hiroyuki [7 ]
Bando, Hiroko [8 ]
Nakamura, Rikiya [9 ]
Yamanaka, Takashi [10 ]
Ishida, Kazushige [11 ]
Aruga, Tomoyuki [12 ]
Yanagita, Yasuhiro [13 ]
Tokunaga, Eriko [14 ]
Aogi, Kenjiro [15 ]
Ohno, Shinji [1 ]
Kasai, Hiroi [16 ]
Kataoka, Tatsuki R. [17 ]
Morita, Satoshi [18 ]
Toi, Masakazu [19 ]
机构
[1] JFCR, Dept Breast Med Oncol, Canc Inst Hosp, Tokyo, Japan
[2] Nagoya Univ, Dept Breast & Endocrine Surg, Grad Sch Med, 65 Tsurumai Cho,Showa Ku, Nagoya, Aichi 4668550, Japan
[3] Hiroshima City Hiroshima Citizens Hosp, Dept Breast Surg, Hiroshima, Japan
[4] Saitama Canc Ctr, Div Breast Oncol, Saitama, Japan
[5] Toranomon Gen Hosp, Dept Med Oncol, Tokyo, Japan
[6] Kyoto Univ Hosp, Dept Breast Surg, Kyoto, Japan
[7] NHO Osaka Natl Hosp, Dept Surg, Breast Oncol, Osaka, Japan
[8] Univ Tsukuba, Fac Med, Breast & Endocrine Surg, Tsukuba, Japan
[9] Chiba Canc Ctr, Div Breast Surg, Chiba, Japan
[10] Kanagawa Canc Ctr, Dept Breast Surg & Oncol, Yokohama, Japan
[11] Iwate Med Univ, Dept Surg, Morioka, Japan
[12] Tokyo Metropolitan Komagome Hosp, Surg Breast, Tokyo, Japan
[13] Gunma Prefectural Canc Ctr, Dept Breast Oncol, Ota, Japan
[14] NHO Kyushu Canc Ctr, Dept Breast Oncol, Fukuoka, Japan
[15] NHO Shikoku Canc Ctr, Dept Breast Oncol, Matsuyama, Japan
[16] Tohoku Univ Hosp, Clin Res Innovat & Educ Ctr, Sendai, Japan
[17] Iwate Med Univ, Dept Diagnost Pathol, Morioka, Japan
[18] Kyoto Univ, Grad Sch Med, Dept Biomed Stat & Bioinformat, Kyoto, Japan
[19] Tokyo Metropolitan Komagome Hosp, Tokyo, Japan
[20] Kyoto Univ, Grad Sch Med, Dept Breast Surg, Kyoto, Japan
关键词
De-escalation; Long-term outcomes; Neoadjuvant therapy; Pertuzumab; Response-guided treatment; Trastuzumab emtansine; FREE CHEMOTHERAPY REGIMENS; DE-ESCALATION STRATEGIES; PREDICTIVE MARKERS; TRIAL-EFFICACY; CARDIAC SAFETY; FINAL ANALYSIS;
D O I
10.1007/s10549-024-07333-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The randomized phase 2 Neo-peaks study examined usefulness of neoadjuvant trastuzumab emtansine + pertuzumab (T-DM1 + P) following docetaxel + carboplatin + trastuzumab + pertuzumab (TCbHP) as compared with the standard TCbHP regimen. We previously reported that pCR rate after neoadjuvant therapy tended to be higher with TCbHP followed by T-DM1 + P. We conducted an exploratory analysis of prognosis 5 years after surgery.Methods Neoadjuvant treatment with TCbHP (6 cycles; group A), TCbHP (4 cycles) followed by T-DM1 + P (4 cycles; group B), and T-DM1 + P (4 cycles; group C, + 2 cycles in responders) were compared. Group C non-responders after 4 cycles were switched to an anthracycline-based regimen. We evaluated 5-year disease-free survival (DFS), distant DFS (DDFS), and overall survival (OS).Results Data from 203 patients (50, 52, and 101 in groups A-C, respectively) were analyzed. No significant intergroup differences were found for DFS, DDFS, or OS. The 5-year DFS rates (95% CI) were 91.8% (79.6-96.8%), 92.3% (80.8-97.0%), and 88.0% (79.9-93.0%) in groups A-C, respectively. TCbHP followed by T-DM1 + P and T-DM1 + P with response-guided addition of anthracycline therapy resulted in similar long-term prognosis to that of TCbHP.Conclusions In patients who achieved pCR after neoadjuvant therapy with T-DM1 + P, omission of adjuvant anthracycline may be considered, whereas treatment should be adjusted for non-pCR patients with residual disease. T-DM1 + P with response-guided treatment adjustment may be useful for minimizing toxicity.Trial registration number and date of registration UMIN-CTR, UMIN000014649, prospectively registered July 25, 2014. Some of the study results were presented as a Mini Oral session at the ESMO Breast Cancer 2023 (Berlin, Germany, 11-13 May 2023).
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页码:33 / 48
页数:16
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