Evidence map›Paper›PMID 35002243›Full record

ArticleBreast cancer : basic and clinical research2022

Clinicopathological Features Related to the Efficacy of CDK4/6 Inhibitor-Based Treatments in Metastatic Breast Cancer.

Ayana Shikanai, Yoshiya Horimoto, Yumiko Ishizuka, Toshitaka Uomori, Katsuya Nakai, Atsushi Arakawa, Mitsue Saito

Open access · goldAbstract read
In one paragraph

Article in Breast cancer : basic and clinical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.4field-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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Ayana ShikanaiDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Yoshiya HorimotoDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8935-0768
Yumiko IshizukaDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Toshitaka UomoriDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Katsuya NakaiDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Atsushi ArakawaDepartment of Human Pathology, School of Medicine, Juntendo University, Tokyo, Japan.
Mitsue SaitoDepartment of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResistance to endocrine therapy has been a major obstacle in the management of hormone receptor (HR)-positive metastatic breast cancer (MBC). Meanwhile, a number of treatments are available to such patients, and physicians often encounter difficulties in choosing the most appropriate treatments for individual patients. The combination of CDK 4/6 inhibitors (CDKi) and endocrine therapy has now become a standard treatment for HR-positive and human epidermal growth factor receptor 2 (HER2)-negative MBC. However, no predictive markers for CDKi-based treatments have been established. Considering their side effects and the financial burden on patients, identifying such markers is crucial.

methodsClinicopathological features of 107 patients with HR-positive HER2-negative MBC, who received CDKi-based treatments at our institution were retrospectively investigated. HR status in distant metastatic lesions and immunocompetent cells in peripheral blood were also studied.

resultsProgression-free survival (PFS) was significantly shorter in patients whose primary tumour was high grade (

conclusionOur data indicate that tumour grade in primary lesion and NLR are potential predictive factors for CDKi-based treatments. Moreover, pathological assessment of metastatic lesions might also be useful.

Indexed as

Breast cancerCDK 4/6 inhibitormetastatic lesionneutrophil-to-lymphocyte ratiopredictive marker

Identifiers

PMID35002243
PMCPMC8738870
OpenAlexW4206167389

What OpenQuestion holds

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LicenceCC BY-NC
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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.