Evidence map›Paper›PMID 36743521›Full record

ArticleTherapeutic advances in medical oncology2023

TRK inhibitor in a patient with metastatic triple-negative breast cancer and

Arielle J Medford, Lauren Oshry, Baris Boyraz, Lesli Kiedrowski, Sofia Menshikova, Anna Butusova, Charles S Dai, Tasos Gogakos, Jennifer C Keenan, Rachel H Occhiogrosso and 6 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Therapeutic advances in medical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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  5. 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

16 authors at 5 institutions in 1 country.

Arielle J MedfordMassachusetts General Hospital Cancer Center, 55 Fruit Street, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0002-0829-183X
Lauren OshryBoston Medical Center, Boston, MA, USA.
Baris BoyrazMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Lesli KiedrowskiGuardant Health, Inc., Redwood City, CA, USA.
Sofia MenshikovaBostonGene Corporation, Boston, MA, USA.
Anna ButusovaBostonGene Corporation, Boston, MA, USA.
Charles S DaiMassachusetts General Hospital Cancer Center, Boston, MA, USA.ORCID https://orcid.org/0000-0003-2615-3286
Tasos GogakosMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Jennifer C KeenanMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Rachel H OcchiogrossoMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Phoebe RyanMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Jochen K LennerzMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Laura M SpringMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Beverly MoyMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Leif W EllisenMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Aditya BardiaMassachusetts General Hospital Cancer Center, Boston, MA, USA.ORCID https://orcid.org/0000-0003-4885-1157
Harvard University · USMassachusetts General Hospital · USAddgene · USBoston Medical Center · USGuardant (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue-agnostic indications for targeted therapies have expanded options for patients with advanced solid tumors. The Food and Drug Administration approvals of the programmed death-ligand 1 inhibitor pembrolizumab and the TRK inhibitors larotrectinib and entrectinib provide rationale for next-generation sequencing (NGS) in effectively all advanced solid tumor patients given potential for clinical responses even in otherwise refractory disease. As proof of concept, this case report describes a 64-year-old woman with triple-negative breast cancer refractory to multiple lines of therapy, found to have a rare mutation on NGS which led to targeted therapy with meaningful response. She initially presented with metastatic recurrence 5 years after treatment for a localized breast cancer, with rapid progression through four lines of therapy in the metastatic setting, including immunotherapy, antibody-drug conjugate-based therapy, and chemotherapy. Germline genetic testing was normal. Ultimately, NGS evaluation of cell-free DNA

Indexed as

blood-based biomarkerbreast cancercase reportpredictive biomarkertargeted therapy

Identifiers

PMID36743521
PMCPMC9893401
OpenAlexW4318713275

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.