Evidence map›Paper›PMID 35207749›Full record

ArticleJournal of personalized medicine2022

Androgen Receptor: A New Marker to Predict Pathological Complete Response in HER2-Positive Breast Cancer Patients Treated with Trastuzumab Plus Pertuzumab Neoadjuvant Therapy.

Jiayi Li, Shuang Zhang, Chen Ye, Qian Liu, Yuanjia Cheng, Jingming Ye, Yinhua Liu, Xuening Duan, Ling Xin, Hong Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 37% of its field
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
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

11 authors at 1 institution in 1 country.

Jiayi LiBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Shuang ZhangDepartment of Pathology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0003-0259-8002
Chen YeSchool of Public Health, Peking University Health Science Center, Haidian District, Beijing 100191, China.
Qian LiuBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Yuanjia ChengBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Jingming YeBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Yinhua LiuBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Xuening DuanBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Ling XinBreast Disease Center, Peking University First Hospital, Beijing 100034, China.
Hong ZhangDepartment of Pathology, Peking University First Hospital, Beijing 100034, China.
Ling XuBreast Disease Center, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-9236-3014
Peking University · CN

Funding

Interdisciplinary Clinical Research Project of Peking University First Hospital 2019CR38National Key R&D Program of China 2016YFC0901302
6 · The paper itself

Abstract

(1) Background: Neoadjuvant therapy is the main therapeutic strategy for human epidermal growth factor receptor 2 (HER2)-positive breast cancer patients, and the combination of trastuzumab and pertuzumab (HP) has become a routine treatment. How to predict and screen patients who are less likely to respond to neoadjuvant therapy is the focus of research. The androgen receptor (AR) is a biomarker that is widely expressed in all breast cancer subtypes and is probably related to treatment response and prognosis. In this study, we investigated the relationship between AR expression and treatment response in HER2-positive breast cancer patients treated with HP neoadjuvant therapy. (2) Methods: We evaluated early breast cancer patients treated with HP neoadjuvant therapy from Jan. 2019 to Oct. 2020 at Peking University First Hospital Breast Cancer Center. The inclusion criteria were as follows: early HER2-positive breast cancer patients diagnosed by core needle biopsy who underwent both HP neoadjuvant therapy and surgery. We compared the clinical and pathological features between pathological complete response (pCR) and non-pCR patients. (3) Results: We included 44 patients. A total of 90.9% of patients received neoadjuvant therapy of taxanes, carboplatin, trastuzumab and pertuzumab (TCHP), and the total pCR rate was 50%. pCR was negatively related to estrogen receptor (ER) positivity (OR 0.075 [95% confidence interval (CI) 0.008-0.678],

Indexed as

androgen receptorbreast cancerneoadjuvant therapypathologic complete responsepertuzumabtrastuzumab

Identifiers

PMID35207749
PMCPMC8877578
OpenAlexW4211109760

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.