Evidence map›Paper›PMID 38213803›Full record

ArticleAnnals of translational medicine2023

Efficacy and safety of tucidinostat in patients with advanced hormone receptor-positive human epidermal growth factor receptor 2-negative breast cancer: real-world insights.

Jiaojiao Suo, Kunrui Zhu, Chunying Zhuang, Xiaorong Zhong, Sara Bravaccini, Roberta Maltoni, François Bertucci, Hong Zheng, Ting Luo

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. ACS pharmacology & translational science · 2025
    Article
  5. Article
  6. Histone acetylation modulators in breast cancer.Breast cancer research : BCR · 2025
    Review
  7. Article
  8. Review
  9. 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

9 authors at 3 institutions in 3 countries.

Jiaojiao Suo *Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Kunrui Zhu *Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Chunying Zhuang *Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Xiaorong ZhongDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Sara BravacciniIRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Roberta MaltoniIRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
François BertucciDepartment of Medical Oncology, Cancer Research Center of Marseille, Paoli-Calmettes Institute, Aix-Marseille University, INSERM UMR1068, CNRS UMR725, Marseille, France.
Hong ZhengDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Ting LuoDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CNIstituti di Ricovero e Cura a Carattere Scientifico · ITInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tucidinostat, which is a subtype-selective histone deacetylase inhibitor, has been approved in China for the treatment of hormone receptor-positive (HR Methods: The objective of this real-world study was to analyze the clinical data of 47 patients with HR Results: A total of 47 patients were included, and the median follow-up time was 18.20 months. The median line of tucidinostat therapy was 3 (range, 1-9). In all, 52.17% patients were treated with tucidinostat plus fulvestrant, while 38.30% were treated with tucidinostat plus aromatase inhibitors. Notably, 10.64% of the patients with rapidly progressing visceral metastases received tucidinostat plus endocrine therapy as maintenance treatment after achieving disease control with chemotherapy. The median PFS was 4.43 months [95% confidence interval (CI), 2.77-10.53], and the median overall survival was 19.57 months (95% CI, 12.83-not reached). The 6-month CBR for the overall population was 41.86%. Patients undergoing maintenance therapy demonstrated a significantly longer PFS than did those who did not receive it as maintenance therapy (14.13 Conclusions: For patients with HR

Indexed as

advanced breast cancer (ABC)hormone receptor-positive (HR+)Tucidinostat

Identifiers

PMID38213803
PMCPMC10777213
OpenAlexW4389942626

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.