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)
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Published:2024-05-20
Issue:1
Volume:207
Page:33-48
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ISSN:0167-6806
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Container-title:Breast Cancer Research and Treatment
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language:en
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Short-container-title:Breast Cancer Res Treat
Author:
Takano ToshimiORCID, Masuda NorikazuORCID, Ito Mitsuya, Inoue Kenichi, Tanabe YukoORCID, Kawaguchi Kousuke, Yasojima Hiroyuki, Bando HirokoORCID, Nakamura RikiyaORCID, Yamanaka Takashi, Ishida KazushigeORCID, Aruga TomoyukiORCID, Yanagita Yasuhiro, Tokunaga Eriko, Aogi Kenjiro, Ohno Shinji, Kasai Hiroi, Kataoka Tatsuki R.ORCID, Morita Satoshi, Toi Masakazu
Abstract
Abstract
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).
Funder
Japan Breast Cancer Research Group
Publisher
Springer Science and Business Media LLC
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