Evidence map›Paper›PMID 41437938›Full record

ArticleTherapeutic advances in medical oncology2025

Trastuzumab and pertuzumab plus carboplatin-based neoadjuvant therapy for HER2-positive breast cancer: a prospective cohort study with integrated genomic and transcriptomic biomarker analysis.

Xiaoyan Qian, Xi Chen, Min Xiao, Lei Ji, Qiao Li, Jiayu Wang, Ying Fan, Yang Luo, Ruigang Cai, Bo Lan and 4 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Xiaoyan QianDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0000-0001-7892-8720
Xi ChenDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0009-0009-4599-5711
Min XiaoDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Lei JiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Qiao LiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Jiayu WangDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0000-0003-1967-389X
Ying FanDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Yang LuoDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Ruigang CaiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Bo LanDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0000-0002-2962-439X
Shanshan ChenDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.
Fei MaDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0000-0001-9432-1902
Binghe XuDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, Beijing, China.ORCID https://orcid.org/0000-0002-6863-5024
Pin ZhangDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 17 Panjiayuan Nanli, Chaoyang District, Beijing 100021, China.ORCID https://orcid.org/0000-0001-8903-3666

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant trastuzumab and pertuzumab combined with carboplatin and taxane (TCbHP) is the standard treatment for human epidermal growth factor receptor 2 (HER2)-positive breast cancer. However, limited clinical data and efficacy biomarkers for TCbHP have been reported in Chinese HER2-positive breast cancer patients. Objectives: This study aimed to observe the pathological complete response (pCR) rate in the cohort, with an exploratory analysis of efficacy-related biomarkers in a subset of patients. Design: This was a prospective, observational, non-interventional cohort study. Methods: Patients with HER2-positive breast cancer treated with TCbHP neoadjuvant therapy were prospectively collected. Exploratory genomic and transcriptomic biomarker analyses were performed in a subset of patients with available baseline tumour specimens retrospectively collected. Results: A total of 252 patients with a median age of 48 years were enrolled. Patients with stage III were 69.4% (175/252), and clinical N3 patients accounted for 24.6% (62/252). Patients with hormone receptor (HR) positive were 62.7% (158/252). Total pCR rate was 55.2% (139/252). HR-negative and HR-positive rates were 72.3% (68/94) and 44.9% (71/158), respectively. Among neoadjuvant taxanes, including paclitaxel, docetaxel, and nab-paclitaxel, the pCR rates were 50.0% (57/114), 50.0% (41/82), and 73.2% (41/56), respectively. Multivariate logistic regression analyses showed that HR negativity, receiving nab-paclitaxel, HER2 3+, and cT1-2 were independent predictive factors of high pCR. Genomic and transcriptomic analyses were performed on baseline tumour specimens from 40 patients. Genomic analysis revealed lower pCR rates in patients with Conclusion: Neoadjuvant trastuzumab and pertuzumab with carboplatin-based chemotherapy is the recommended regimen for Chinese patients with HER2-positive breast cancer, and nab-paclitaxel may be an optimal alternative taxane for TCbHP regimens.

Indexed as

biomarkersbreast cancerefficacyHER2-positiveneoadjuvant therapy

Identifiers

PMID41437938
PMCPMC12719586

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.