Evidence map›Paper›PMID 34485698›Full record

ArticleExpert review of precision medicine and drug development2021

Novel insights into the pathogenesis and treatment of NRAS mutant melanoma.

Jeffrey Zhao, Carlos Galvez, Kathryn Eby Beckermann, Douglas B Johnson, Jeffrey A Sosman

Abstract read
In one paragraph

Article in Expert review of precision medicine and drug development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
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

5 authors.

Jeffrey ZhaoNorthwestern University Feinberg School of Medicine.
Carlos GalvezNorthwestern Medicine, Division of Hematology and Oncology.
Kathryn Eby BeckermannVanderbilt University Medical Center, Department of Medicine, Division of Hematology and Oncology, 1301 Medical Center Drive, Nashville, 37232, USA.
Douglas B JohnsonVanderbilt University Medical Center, Department of Medicine, Division of Hematology and Oncology, 1301 Medical Center Drive, Nashville, 37232, USA.
Jeffrey A SosmanNorthwestern Medicine, Division of Hematology and Oncology.

Funding

Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
Princess Margaret Phase I Consorium (PMP1C)UM1CA186644 · NCI · UNIVERSITY HEALTH NETWORK · PI Philippe Bedard, Kevin D Courtney · 2014 to 2026
$16.6M
Long-Term Cardiovascular Sequelae of Cancer ImmunotherapiesR01HL155990 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOHNSON, DOUGLAS B, MOSLEHI, JAVID J · 2021 to 2025
$3.3M
(PQ8) Patient- and tumor-specific biomarkers and mechanisms that predict irAEs resulting from checkpoint inhibitionR01CA227481 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BALKO, JUSTIN M, JOHNSON, DOUGLAS B · 2019 to 2023
$2.6M
The distinct role of cysteinyl leukotriene receptor for myeloid-derived suppressive cellsR01CA250101 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2020 to 2025
$2.5M
WEE1 inhibition and tumor immunityR01CA222963 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2018 to 2023
$2.2M
The role of GPSM3 in tumor-promoting emergency myelopoiesisR01CA208354 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2017 to 2021
$1.8M
An In Silico, Medical Record-based Model for Understanding the INitiation of Autoimmune Events (IMMUNE)R61AR076824 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KHO, ABEL N., WALUNAS, THERESA L · 2019 to 2019
$395k
NCI NIH HHS K12 CA090625NCI NIH HHS R01 CA208354NCI NIH HHS R01 CA222963NCI NIH HHS R01 CA227481NCI NIH HHS R01 CA250101NCI NIH HHS UM1 CA186644NHLBI NIH HHS R01 HL155990NIAMS NIH HHS R61 AR076824
6 · The paper itself

Abstract

introductionNRAS was the first mutated oncogene identified in melanoma and is currently the second most common driver mutation in this malignancy. For patients with NRAS AREAS COVERED: This review surveys new developments in all aspects of disease pathogenesis and potential treatment - including those that have failed, stalled, or progressed through various phases of preclinical and clinical development. EXPERT OPINION: There are no currently approved targeted therapies for BRAF wild-type melanoma patients harboring NRAS driver mutations though an array of agents are in early phase clinical trials. The diverse strategies taken exploit combined MAP kinase signaling blockade with inhibition of cell cycle mediators, inhibition of the autophagy pathway, and alteration of kinases involved in actin cytoskeleton signaling. Future advances of developmental therapeutics into late stage trials may yield new options beyond immunotherapy for patients with advanced stage disease and NRAS mutation status.

Indexed as

clinical trialsdrug developmentgenomicsmelanocytemelanomamolecular geneticsNRASoncologypharmacologyprecision medicinetargeted therapiestumor biology

Identifiers

PMID34485698
PMCPMC8415440

What OpenQuestion holds

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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.