Evidence map›Paper›PMID 41727688›Full record

ArticleFrontiers in endocrinology2026

BRAF and MEK inhibition beyond dabrafenib-trametinib in advanced thyroid cancer: a real-world case series.

Tzahi Yamin, Oded Cohen, Eyal Robenshtok, Elena Izkhakov, Mor Miodovnik, Orit Gutfeld, Yasmin Leshem, Roman Meirovitz, Anton Warshavsky, Nidal Muhanna and 1 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Tzahi YaminDepartment of Otolaryngology, Head and Neck Surgery, Assuta Samson Ashdod Medical Center, Ashdod, Israel.
Oded CohenDepartment of Otolaryngology, Head and Neck Surgery, Assuta Samson Ashdod Medical Center, Ashdod, Israel.
Eyal RobenshtokEndocrinology and Metabolism Institute and Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Elena IzkhakovInstitute of Endocrinology, Metabolism and Hypertension, Sourasky Medical Center, Tel Aviv, Israel.
Mor MiodovnikOncology Division, Sourasky Medical Center, Tel Aviv, Israel.
Orit GutfeldOncology Division, Sourasky Medical Center, Tel Aviv, Israel.
Yasmin LeshemOncology Division, Sourasky Medical Center, Tel Aviv, Israel.
Roman MeirovitzOncology Division, Sourasky Medical Center, Tel Aviv, Israel.
Anton WarshavskyDepartment of Otolaryngology, Head and Neck Surgery and Maxillofacial Surgery, Sourasky Medical Center, Tel Aviv, Israel.
Nidal MuhannaDepartment of Otolaryngology, Head and Neck Surgery and Maxillofacial Surgery, Sourasky Medical Center, Tel Aviv, Israel.
Inbar FinkelOncology Division, Sourasky Medical Center, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: BRAF V600E mutation is the most common and clinically significant genetic alteration in advanced thyroid cancers. This study provides real-world experience with BRAF and MEK inhibitors other than dabrafenib and trametinib in the treatment of advanced thyroid cancers harboring this mutation. Methods: A case series of four patients with advanced thyroid cancer (three papillary and one anaplastic) treated with various BRAF and MEK inhibitors. All patients had confirmed BRAF V600E mutation. Results: Among three patients treated with BRAF/MEK inhibitors for radioiodine refractory metastatic PTC, and one patient with ATC, all (100%) demonstrated a partial response (PR) during therapy, yielding an overall response rate (ORR) of 100%. Stable disease was observed in multiple treatment phases, contributing to a high overall disease control rate. Three patients had disease-related death, while one remained under treatment at last follow-up. The course of treatment was complicated by significant toxicities, leading to dose reductions or treatment discontinuations. Despite initial responses, all cases eventually progressed, necessitating sequential treatment strategies. Overall survival ranged from 6.0 to 25.3 months, with a median follow-up of 18.3 months since the initiation of BRAF and MEK inhibitors. Conclusions: This case series highlights the potential benefits and challenges of targeted therapies in advanced thyroid cancer. While BRAF and MEK inhibitors offer new treatment options, toxicity management and the development of resistance remain significant hurdles. The limited FDA-approved options for BRAF V600E-positive thyroid cancer compared to melanoma underscore the need for further research to optimize and expand treatment strategies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsProtein Kinase InhibitorsProto-Oncogene Proteins B-rafThyroid NeoplasmsAdultAgedFemaleHumansImidazolesMaleMiddle AgedMutationOximesPyridonesPyrimidinonesBRAF protein, humandabrafenibImidazolesOximesProtein Kinase InhibitorsProto-Oncogene Proteins B-rafPyridonesPyrimidinonestrametinibanaplastic thyroid carcinomaBRAF V600E mutationpapillary thyroid carcinomareal-world evidencetargeted therapy

Identifiers

PMID41727688
PMCPMC12916350

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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.