Short-term efficacy and safety of neoadjuvant pyrotinib plus taxanes for early HER2-positive breast cancer: a single-arm exploratory phase II trial.

Pyrotinib breast cancer (BC) chemotherapy human epidermal growth factor receptor 2 (HER2) neoadjuvant therapy

Journal

Gland surgery
ISSN: 2227-684X
Titre abrégé: Gland Surg
Pays: China (Republic : 1949- )
ID NLM: 101606638

Informations de publication

Date de publication:
27 Mar 2024
Historique:
received: 29 01 2024
accepted: 13 03 2024
medline: 11 4 2024
pubmed: 11 4 2024
entrez: 11 4 2024
Statut: ppublish

Résumé

The effectiveness and safety of pyrotinib have been substantiated in human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer (BC). However, the role of pyrotinib as a single HER2 blockade in neoadjuvant setting among BC patients has not been studied. The objective of this study was to evaluate the efficacy and tolerability of pyrotinib plus taxanes as a novel neoadjuvant regimen in patients with HER2-positive early or locally advanced BC. In this single-arm exploratory phase II trial, patients with treatment-naïve HER2-positive BC (stage IIA-IIIC) received pyrotinib 400 mg once daily and taxanes [docetaxel 75 mg/m From 1 September 2021 to 30 December 2022, a total of 31 patients were enrolled. One patient was withdrawn due to unbearable skin rash after the second cycle of neoadjuvant therapy. The majority of the intention-to-treat (ITT) population was premenopausal (54.8%), had large tumors (90.3%) and metastatic nodes (58.1%) at diagnosis and hormone-receptor positive tumors (64.5%). Most participants used nab-paclitaxel (74.2%) and received mastectomy (67.7%) after neoadjuvant treatment. The tpCR and bpCR rates were 48.4% [95% confidence interval (CI): 30.8-66%] and 51.6% (95% CI: 34-69.2%), respectively. Grade ≥3 treatment-related AEs were observed in 16.1% (5/31) of the ITT population, including diarrhea (n=2, 6.5%), hand and foot numbness (n=1, 3.2%), loss of appetite (n=1, 3.2%), and skin rash (n=1, 3.2%). AE related dose reduction or pyrotinib interruption was not required. In female patients with HER2-positive non-metastatic BC, neoadjuvant pyrotinib monotherapy plus taxanes appears to show promising clinical benefit and controllable AEs [Chinese Clinical Trial Registry (ChiCTR2100050870)]. The long-term efficacy and safety of this regime warrant further verification.

Sections du résumé

Background UNASSIGNED
The effectiveness and safety of pyrotinib have been substantiated in human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer (BC). However, the role of pyrotinib as a single HER2 blockade in neoadjuvant setting among BC patients has not been studied. The objective of this study was to evaluate the efficacy and tolerability of pyrotinib plus taxanes as a novel neoadjuvant regimen in patients with HER2-positive early or locally advanced BC.
Methods UNASSIGNED
In this single-arm exploratory phase II trial, patients with treatment-naïve HER2-positive BC (stage IIA-IIIC) received pyrotinib 400 mg once daily and taxanes [docetaxel 75 mg/m
Results UNASSIGNED
From 1 September 2021 to 30 December 2022, a total of 31 patients were enrolled. One patient was withdrawn due to unbearable skin rash after the second cycle of neoadjuvant therapy. The majority of the intention-to-treat (ITT) population was premenopausal (54.8%), had large tumors (90.3%) and metastatic nodes (58.1%) at diagnosis and hormone-receptor positive tumors (64.5%). Most participants used nab-paclitaxel (74.2%) and received mastectomy (67.7%) after neoadjuvant treatment. The tpCR and bpCR rates were 48.4% [95% confidence interval (CI): 30.8-66%] and 51.6% (95% CI: 34-69.2%), respectively. Grade ≥3 treatment-related AEs were observed in 16.1% (5/31) of the ITT population, including diarrhea (n=2, 6.5%), hand and foot numbness (n=1, 3.2%), loss of appetite (n=1, 3.2%), and skin rash (n=1, 3.2%). AE related dose reduction or pyrotinib interruption was not required.
Conclusions UNASSIGNED
In female patients with HER2-positive non-metastatic BC, neoadjuvant pyrotinib monotherapy plus taxanes appears to show promising clinical benefit and controllable AEs [Chinese Clinical Trial Registry (ChiCTR2100050870)]. The long-term efficacy and safety of this regime warrant further verification.

Identifiants

pubmed: 38601287
doi: 10.21037/gs-24-38
pii: gs-13-03-374
pmc: PMC11002487
doi:

Types de publication

Journal Article

Langues

eng

Pagination

374-382

Informations de copyright

2024 Gland Surgery. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://gs.amegroups.com/article/view/10.21037/gs-24-38/coif). The authors have no conflicts of interest to declare.

Auteurs

Guolin Ye (G)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Peixian Chen (P)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Xiangwei Liu (X)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Tiancheng He (T)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Xavier Pivot (X)

Medical Oncology Department, Institute of Cancerology Strasbourg Europe (ICANS), Strasbourg, France.

Ruilin Pan (R)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Dan Zhou (D)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Lewei Zhu (L)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Kun Zhang (K)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Wei Li (W)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Shuqing Yang (S)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Jiawei Lin (J)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Gengxi Cai (G)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Huiqi Huang (H)

Department of Breast Surgery, The First People's Hospital of Foshan, Foshan, China.

Classifications MeSH