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DOI 10.1007/s10549-024-07333-7

Медицинская библиотека · Breast cancer research and treatment · 2024

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

Takano Toshimi, Masuda Norikazu, Ito Mitsuya, Inoue Kenichi, Tanabe Yuko, Kawaguchi Kousuke, Yasojima Hiroyuki, Bando Hiroko, Nakamura Rikiya, Yamanaka Takashi, Ishida Kazushige, Aruga Tomoyuki, Yanagita Yasuhiro, Tokunaga Eriko, Aogi Kenjiro, Ohno Shinji, Kasai Hiroi, Kataoka Tatsuki R, Morita Satoshi, Toi Masakazu

СтатьяКлиническое исследование II фазыРандомизированное исследованиеПеревод в очереди

Аннотация

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).

Для цитирования: Takano Toshimi, Masuda Norikazu, Ito Mitsuya, Inoue Kenichi, Tanabe Yuko, Kawaguchi Kousuke, Yasojima Hiroyuki, Bando Hiroko, Nakamura Rikiya, Yamanaka Takashi, Ishida Kazushige, Aruga Tomoyuki, Yanagita Yasuhiro, Tokunaga Eriko, Aogi Kenjiro, Ohno Shinji, Kasai Hiroi, Kataoka Tatsuki R, Morita Satoshi, Toi Masakazu. Long-term outcomes of neoadjuvant trastuzumab emtansine + pertuzumab (T-DM1 + P) and docetaxel + carboplatin + trastuzumab + pertuzumab (TCbHP) for HER2-positive primary breast cancer: results of the randomized phase 2 JBCRG20 study (Neo-peaks).. Breast cancer research and treatment. 2024. DOI: 10.1007/s10549-024-07333-7.

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