Evidence map›Paper›PMID 37141549›Full record

ArticleJCO precision oncology2023

Cyclin-Dependent Kinase 4/6 Inhibitors Beyond Progression in Metastatic Breast Cancer: A Retrospective Real-World Biomarker Analysis.

Lorenzo Gerratana, Andrew A Davis, Marko Velimirovic, Carolina Reduzzi, Katherine Clifton, Leslie Bucheit, Whitney L Hensing, Ami N Shah, Tania Pivetta, Charles S Dai and 10 more

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 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

20 authors at 7 institutions in 2 countries.

Lorenzo GerratanaDepartment of Medical Oncology, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.ORCID 0000-0002-8313-4834
Andrew A DavisDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.ORCID 0000-0003-4036-686X
Marko VelimirovicMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-1406-9469
Carolina ReduzziWeill Cornell Medicine, New York, NY.ORCID 0000-0003-0514-0152
Katherine CliftonDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.ORCID 0000-0001-8623-995X
Leslie BucheitGuardant Health, Redwood City, CA.ORCID 0000-0001-8826-0357
Whitney L HensingDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Ami N ShahFeinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0003-1347-3782
Tania PivettaDepartment of Medical Oncology, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
Charles S DaiMassachusetts General Hospital, Boston, MA.ORCID 0000-0003-2615-3286
Paolo D'AmicoFeinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0001-9155-425X
Firas WehbeFeinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-3984-9584
Arielle MedfordMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-0829-183X
Seth A WanderMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-4127-4708
William J GradisharFeinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-2772-3140
Amir BehdadFeinberg School of Medicine, Northwestern University, Chicago, IL.
Cynthia X MaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.ORCID 0000-0002-8156-7492
Fabio PuglisiDepartment of Medical Oncology, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.ORCID 0000-0003-0573-4938
Aditya BardiaMassachusetts General Hospital, Boston, MA.ORCID 0000-0003-4885-1157
Massimo CristofanilliWeill Cornell Medicine, New York, NY.ORCID 0000-0002-4194-7175
Harvard University · USNorthwestern University · USWashington University in St. Louis · USCornell University · USUniversity of Udine · ITCentro di Riferimento Oncologico · ITGuardant (United States) · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
NCATS NIH HHS UL1 TR001422
6 · The paper itself

Abstract

purposeAs the continuation beyond progression (BP) of cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) is becoming increasingly attractive for the treatment of patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (MBC), the definition of resistance factors is crucial. The aim of the study was to investigate the impact of CDK 4/6i BP and to explore potential genomic stratification factors. MATERIALS AND

methodsWe retrospectively analyzed a multi-institutional cohort of patients with HR-positive HER2-negative MBC characterized for circulating tumor DNA through next-generation sequencing before treatment start. Differences across subgroups were analyzed by chi-square test, and survival was tested by univariable and multivariable Cox regression. Further correction was applied by propensity score matching.

resultsAmong the 214 patients previously exposed to CDK4/6i, 172 were treated with non-CDK4/6i-based treatment (non-CDK) and 42 with CDK4/6i BP. Multivariable analysis showed a significant impact of CDK4/6i BP, TP53 single-nucleotide variants, liver involvement, and treatment line on both progression-free survival (PFS) and overall survival (OS). Propensity score matching confirmed the prognostic role of CDK4/6i BP both for PFS and OS. The favorable impact of CDK4/6i BP was consistent across all subgroups, and a differential benefit was suggested for

conclusionThe study highlighted a significant prognostic impact of the CDK4/6i BP strategy with a potential added benefit in patients with

Indexed as

Breast NeoplasmsCirculating Tumor DNACyclin-Dependent Kinase 4FemaleGenomicsHumansRetrospective StudiesCirculating Tumor DNACyclin-Dependent Kinase 4

Identifiers

PMID37141549
PMCPMC10309576
OpenAlexW4368343477

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.