Evidence map›Paper›PMID 32233990›Full record

ReviewCancer biology & therapy2020

Significant response to apatinib monotherapy in heavily pretreated advanced HER2-positive breast cancer: a case report and literature review.

Li Danni, Zhang Lingyun, Wang Jian, Yan Hongfei, Xu Lu, Yang Peng, Qu Xiujuan, Liu Yunpeng, Teng Yuee

Open access · bronzeAbstract readCase ReportsReview
In one paragraph

Review in Cancer biology & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

9 authors at 1 institution in 1 country.

Li DanniDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Zhang LingyunDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Wang JianDepartment of Pathology, The First Hospital of China Medical University , Shenyang, China.
Yan HongfeiDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Xu LuDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Yang PengNanjing Geneseeq Technology Inc , Nanjing, China.
Qu XiujuanDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Liu YunpengDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.
Teng YueeDepartment of Medical Oncology, The First Hospital of China Medical University , Shenyang, China.ORCID 0000-0002-9198-9795
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although HER2-targeted therapy has been shown to prolong the survival of patients with HER2-positive breast cancer, most patients eventually progress due to drug resistance. Novel treatment options are urgently needed to overcome resistance to HER2-targeted therapy. The VEGF/VEGFR (Vascular endothelial growth factor and its receptors) pathway is essential in tumor angiogenesis, which may be a promising target in HER2-positive breast cancer providing a rationale for the use of tyrosine kinase inhibitors (TKIs) targeting VEGFR. Here, we present a case of a heavily pretreated advanced breast cancer patient who did not respond to HER2-targeted therapy and developed resistance to multiple lines of HER2-targeted treatment. The patient was treated with apatinib at a dose of 500 mg daily, and obtained partial remission (PR) with a progression-free-stage (PFS) of 6 months. Our case indicates that apatinib might have anti-tumor activity in patients with HER2-positive breast cancer with HER2-targeted resistance. This case is of value which may provide new insights into strategies for HER2-targeted therapy resistance options in the clinic.

Indexed as

AdultAntineoplastic AgentsBreast NeoplasmsFemaleHumansPyridinesAntineoplastic AgentsapatinibPyridinesangiogenesisApatinibbreast cancercase reportHER2VEGFR2

Identifiers

PMID32233990
PMCPMC7515454
OpenAlexW3014655733

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.