Evidence map›Paper›PMID 32019858›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Tumor Mutational Burden and

Romualdo Barroso-Sousa, Tanya E Keenan, Sonia Pernas, Pedro Exman, Esha Jain, Ana C Garrido-Castro, Melissa Hughes, Brittany Bychkovsky, Renato Umeton, Janet L Files and 11 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 3 pooled it
12.4field-weighted citation impact, top 1% 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

117 citing papers in PubMed, 3 syntheses or guidelines pooled it, 183 citations in OpenAlex.

  1. Pooled it
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  10. Reprogramming the Immune Landscape of Inflammatory Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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57 more citing papers are in PubMed but not listed here.

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

21 authors at 4 institutions in 2 countries.

Romualdo Barroso-Sousa *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-1825-9876
Tanya E Keenan *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Sonia PernasDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-1485-5080
Pedro ExmanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Esha JainDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Ana C Garrido-CastroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-5989-6636
Melissa HughesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Brittany BychkovskyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Renato UmetonDepartment of Informatics and Analytics, Dana-Farber Cancer Institute, Boston, Massachusetts.
Janet L FilesPathology, Brigham and Women's Hospital, Boston, Massachusetts.
Neal I LindemanPathology, Brigham and Women's Hospital, Boston, Massachusetts.
Laura E MacConaillPathology, Brigham and Women's Hospital, Boston, Massachusetts.
F Stephen HodiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Ian E KropDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Deborah DillonPathology, Brigham and Women's Hospital, Boston, Massachusetts.
Eric P WinerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-8819-1723
Nikhil WagleDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Nancy U LinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-2263-5413
Elizabeth A MittendorfHarvard Medical School, Boston, Massachusetts.
Eliezer M Van Allen *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. sara_tolaney@dfci.harvard.edu eliezerm_vanallen@dfci.harvard.edu.
Sara M Tolaney *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. sara_tolaney@dfci.harvard.edu eliezerm_vanallen@dfci.harvard.edu.
Harvard University · USBrigham and Women's Hospital · USDana-Farber Cancer Institute · USBroad Institute · US

Funding

Tissue and Pathology CoreP50CA168504 · NCI · DANA-FARBER CANCER INST · PI MYLES A BROWN · 2013 to 2026
$30.1M
NCI NIH HHS P50 CA168504
6 · The paper itself

Abstract

purposeFew patients with metastatic triple-negative breast cancer (mTNBC) benefit from immune checkpoint inhibitors (ICI). On the basis of immunotherapy response correlates in other cancers, we evaluated whether high tumor mutational burden (TMB) ≥10 nonsynonymous mutations/megabase and EXPERIMENTAL

designWe identified patients with mTNBC, who consented to targeted DNA sequencing and were treated with ICIs on clinical trials between April 2014 and January 2019 at Dana-Farber Cancer Institute (Boston, MA). Objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) were correlated with tumor genomic features.

resultsSixty-two women received anti-PD-1/L1 inhibitors alone (23%) or combined with targeted therapy (19%) or chemotherapy (58%). High TMB (18%) was associated with significantly longer PFS (12.5 vs. 3.7 months;

conclusionsAmong patients with mTNBC treated with anti-PD-1/L1 therapies, high TMB and

Indexed as

MutationAdultAgedB7-H1 AntigenBiomarkers, TumorCohort StudiesFemaleFollow-Up StudiesHumansImmune Checkpoint InhibitorsImmunotherapyMiddle AgedPrognosisProgrammed Cell Death 1 ReceptorPTEN PhosphohydrolaseSurvival RateB7-H1 AntigenBiomarkers, TumorCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID32019858
PMCPMC7269810
OpenAlexW3004453915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.