Evidence map›Paper›PMID 35875816›Full record

ArticleEClinicalMedicine2022

Subtyping of metastatic breast cancer based on plasma circulating tumor DNA alterations: An observational, multicentre platform study.

Zhe-Yu Hu, Yu Tang, Liping Liu, Ning Xie, Can Tian, Binliang Liu, Lixin Zou, Wei Zhou, Yikai Wang, Xuefeng Xia and 1 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05079074 (Clinical Application of Circulating Tumor DNA), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 36% 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.

NCT05079074 completednot on this map

Clinical Application of Circulating Tumor DNA (ctDNA) to Monitor the Molecular Tumor Burden in Patients With Late-stage Breast Cancer

TypeobservationalSponsorHunan Cancer HospitalRan2016 to 2021Enrolled223ConditionsMetastatic Breast Cancer, Circulating Tumor DNA, Gene AbnormalityArmsctDNA testing
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Omics-Based Investigations of Breast Cancer.Molecules (Basel, Switzerland) · 2023
    Review
  3. Article
  4. Observational
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 3 institutions in 2 countries.

Zhe-Yu HuDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Yu TangDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Liping LiuDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Ning XieDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Can TianDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Binliang LiuDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Lixin ZouThe Forth Hospital of Changsha/Changsha Hospital of Hunan Normal University, Changsha, 410000, China.
Wei ZhouZhuzhou Central Hospital/Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou, 412007, China.
Yikai WangDepartment of Biostatistics and Bioinformatics, Emory University Rollins School of Public Health, Atlanta, 30322, US.
Xuefeng XiaGeneplus-Beijing Institute, Beijing, 102206, China.
Quchang OuyangDepartment of Breast Cancer Medical Oncology, Hunan Cancer Hospital, Changsha, 410013, China.
Central South University · CNEmory University · USHunan Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: After multiple lines of therapies, no guideline or consensus is currently available for the treatment of patients with metastatic breast cancer. This study aims to evaluate the efficacy of a novel re-subtyping and treatment strategy based on ctDNA alterations. Methods: This observational, multicentre study recruited 223 patients with metastatic breast cancer intending to receive late-line therapy from Dec 1, 2016, to June 31, 2019. This study took place in Hunan Cancer Hospital, the Forth Hospital of Changsha and Zhuzhou Central Hospital in China. ctDNA alterations were assessed by next-generation sequencing (NGS). Patients with druggable ctDNA alterations were treated with corresponding targeted drugs which are clinically available. Other patients received physician-chosen treatment. This study was registered with ClinicalTrials.gov, NCT05079074. Findings: The progression-free survival (hazard ratio: 0.45, 95% Confidence Interval (CI): 0.33-0.62, Interpretation: After multiline traditional pathological HR/HER2 subtype-guided therapies, ctDNA testing could identify druggable ctDNA alterations to guide late-line therapy for patients with metastatic breast cancer. Funding: This work was supported by Key Grants of Research and Development in Hunan Province (2018SK2124, 2018SK2120), Natural Science Foundation of Hunan (2019JJ50360), Hunan Provincial Health Commission Project (B2019085, B2019089 and C2019070), and Changsha Science and Technology Project (kq2004125 and kq2004137).

Indexed as

Disease control rate (DCR)Druggable circulating tumor DNA alterationsGenetic alterations of functional pathwaysLate-line therapyProgression-free survival (PFS)

Identifiers

PMID35875816
PMCPMC9304912
OpenAlexW4285725625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.