Evidence map›Paper›PMID 37260297›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

Additional Oncogenic Alterations in RAS-Driven Differentiated Thyroid Cancers Associate with Worse Clinicopathologic Outcomes.

Athanasios Bikas, Sara Ahmadi, Theodora Pappa, Ellen Marqusee, Kristine Wong, Matthew A Nehs, Nancy L Cho, Jacob Haase, Gerard M Doherty, Kartik Sehgal and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. The Molecular Heterogeneity of NRAS Variants in Thyroid Nodules.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2026
    Article
  3. [Inhibitory effect of lonafarnib on anaplastic thyroid carcinoma cells and xenograft tumor growth in nude mice].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2026
    Article
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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

13 authors at 2 institutions in 1 country.

Athanasios BikasDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-6362-3772
Sara AhmadiDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-0566-6771
Theodora PappaDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-5336-9117
Ellen MarquseeDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-6004-0616
Kristine WongHarvard Medical School, Boston, Massachusetts.ORCID 0000-0003-4139-1581
Matthew A NehsHarvard Medical School, Boston, Massachusetts.ORCID 0000-0002-5671-9749
Nancy L ChoHarvard Medical School, Boston, Massachusetts.ORCID 0009-0006-8381-2929
Jacob HaaseDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0003-0960-6546
Gerard M DohertyHarvard Medical School, Boston, Massachusetts.ORCID 0009-0001-9722-4144
Kartik SehgalHarvard Medical School, Boston, Massachusetts.ORCID 0000-0003-4391-6943
Justine A BarlettaHarvard Medical School, Boston, Massachusetts.ORCID 0000-0002-7167-4358
Erik K AlexanderDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-1313-2462
Iñigo LandaDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-2817-8295
Brigham and Women's Hospital · USHarvard University · US

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
TERT transcriptional deregulation in thyroid cancer progressionK22CA230381 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI LANDA-LOPEZ, INIGO · 2020 to 2022
$587k
NCATS NIH HHS UL1 TR002541NCI NIH HHS K22 CA230381
6 · The paper itself

Abstract

purposeRAS mutations occur across the spectrum of thyroid neoplasms, and more tools are needed for better prognostication. The objective of this study was to evaluate how additional genetic events affecting key genes modify prognosis in patients with RAS-mutant thyroid cancers, and specifically differentiated thyroid cancers (DTC). EXPERIMENTAL

designWe performed a clinical-genomic analysis of consecutive patients with DTC, poorly differentiated (PDTC), or anaplastic thyroid cancer (ATC) between January 2014 and December 2021, in whom a custom-targeted next-generation sequencing assay was performed. Patients harboring RAS mutations were included, and we compared their clinical features and outcomes based upon the presence of additional oncogenic alterations.

resultsSeventy-eight patients were identified, with 22% (17/78) harboring a driver RAS mutation plus an additional oncogenic alteration. All six (100%) ATCs had an additional mutation. Compared with DTCs harboring a solitary RAS mutation, patients with DTC with RAS and additional mutation(s) were more likely to be classified as American Thyroid Association high-risk of recurrence (77% vs. 12%; P < 0.001) and to have larger primary tumors (4.7 vs. 2.5 cm; P = 0.002) and advanced stage (III or IV) at presentation (67% vs. 3%; P < 0.001). Importantly, over an average 65-month follow-up, DTC-specific-mortality was more than 10-fold higher (20% vs. 1.8%; P = 0.011) when additional mutations were identified.

conclusionsIdentification of key additional mutations in patients with RAS-mutant thyroid cancers confers a more aggressive phenotype, increases mortality risk in DTC, and can explain the diversity of RAS-mutated thyroid neoplasia. These data support genomic profiling of DTCs to inform prognosis and clinical decision-making.

Indexed as

AdenocarcinomaThyroid Carcinoma, AnaplasticThyroid NeoplasmsHumansMutationPrognosisProto-Oncogene Proteins B-rafProto-Oncogene Proteins B-raf

Identifiers

PMID37260297
PMCPMC10524472
OpenAlexW4376641969

What OpenQuestion holds

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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.