Evidence map›Paper›PMID 28934759›Full record

ArticleBritish journal of cancer2017

Clinically significant mutations in HIV-infected patients with lung adenocarcinoma.

Jonathan Thaler, Carlie Sigel, Mary Beth Beasley, Juan Wisnivesky, Kristina Crothers, Joshua Bauml, Kristen Hysell, Brinda Emu, Laetitia Borsu, Keith Sigel

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 5 institutions in 1 country.

Jonathan ThalerDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Carlie SigelDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Mary Beth BeasleyDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Juan WisniveskyDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Kristina CrothersDepartment of Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA.
Joshua BaumlDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Kristen HysellDepartment of Medicine, Yale University School of Medicine, New Haven, CT 06510, USA.
Brinda EmuDepartment of Medicine, Yale University School of Medicine, New Haven, CT 06510, USA.
Laetitia BorsuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Keith SigelDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Icahn School of Medicine at Mount Sinai · USMemorial Sloan Kettering Cancer Center · USYale University · USUniversity of Pennsylvania · USUniversity of Washington · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Benefits and Harms of Lung Cancer Screening in HIV InfectionR01CA173754 · NCI · UNIVERSITY OF WASHINGTON · PI BRAITHWAITE, RONALD SCOTT, CROTHERS, KRISTINA ANNE · 2013 to 2017
$2.5M
Optimizing Lung Cancer Treatment in HIV Infected PersonsR01CA210806 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIGEL, KEITH MAGNUS · 2017 to 2020
$2.3M
The Cost-Effectiveness of Lung Cancer Screening in HIV InfectionK07CA180782 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIGEL, KEITH MAGNUS · 2014 to 2018
$646k
NCATS NIH HHS UL1 TR001863NCI NIH HHS K07 CA180782NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA173754NCI NIH HHS R01 CA210806
6 · The paper itself

Abstract

backgroundLung cancer is a major cause of death in HIV-infected (HIV+) persons. In this study, we compared the prevalence of tumour EGFR and KRAS mutations in a cohort of lung adenocarcinoma patients by HIV status.

methodsWe collected data from 55 HIV+ patients with lung adenocarcinoma matched to 136 uninfected comparators. We compared the prevalence of EGFR and KRAS mutations by HIV status. We then compared survival by HIV status and by cancer mutation status among HIV+ subjects.

resultsPresence of KRAS and EGFR genetic alterations did not vary by HIV status (all P>0.1). There was no difference in overall survival by HIV status or by mutation status among HIV+ subjects.

conclusionsWe found no major differences in the prevalence of EGFR or KRAS lung adenocarcinoma mutations by HIV status, suggesting that mutational testing should be conducted similarly regardless of the HIV status.

Indexed as

MutationAdenocarcinomaBiomarkers, TumorCohort StudiesErbB ReceptorsFemaleFollow-Up StudiesHIV-1HIV InfectionsHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingPrognosisProto-Oncogene Proteins p21(ras)Biomarkers, TumorEGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID28934759
PMCPMC5672933
OpenAlexW2759060165

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.