Evidence map›Paper›PMID 35072744›Full record

ArticleCancer immunology, immunotherapy : CII2022

Divergent prognostic effects of pre-existing and treatment-emergent thyroid dysfunction in patients treated with immune checkpoint inhibitors.

Mitchell S von Itzstein, Amrit S Gonugunta, Yiqing Wang, Thomas Sheffield, Rong Lu, Sadia Ali, Farjana J Fattah, Donglu Xie, Jennifer Cai, Yang Xie and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  11. The Combined Effect of Immune Checkpoint Inhibitors and Tyrosine Kinase Inhibitors on Thyroid Function.Thyroid : official journal of the American Thyroid Association · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Mitchell S von ItzsteinDepartment of Internal Medicine, Division of Hematology and Oncology, Harold C. Simmons Comprehensive Cancer Center, University of Texas, Southwestern Medical Center, 5323 Harry Hines Blvd., Mail Code 8852, Dallas, TX, 75390-8852, USA.
Amrit S GonuguntaSchool of Medicine, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Yiqing WangDepartment of Population and Data Sciences, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Thomas SheffieldDepartment of Population and Data Sciences, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Rong LuDepartment of Population and Data Sciences, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Sadia AliDepartment of Internal Medicine, Division of Endocrinology, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Farjana J FattahHarold C. Simmons Comprehensive Cancer Center, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Donglu XieAcademic Information Systems, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Jennifer CaiAcademic Information Systems, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
Yang XieHarold C. Simmons Comprehensive Cancer Center, University of Texas, Southwestern Medical Center, Dallas, TX, 75390, USA.
David E GerberDepartment of Internal Medicine, Division of Hematology and Oncology, Harold C. Simmons Comprehensive Cancer Center, University of Texas, Southwestern Medical Center, 5323 Harry Hines Blvd., Mail Code 8852, Dallas, TX, 75390-8852, USA. david.gerber@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USPalo Alto University · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
Cancer Biology Training GrantT32CA124334 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 2007 to 2021
$5.3M
Finding the optimal balance of immunotherapy efficacy and toxicity.U01AI156189 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC, WAKELAND, EDWARD K. · 2020 to 2024
$3.1M
Development of New Cancer Treatments and InvestigatorsK24CA201543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC · 2016 to 2020
$737k
Harold C. Simmons Comprehensive Cancer Center Data Sciences Shared Resource 1P30 CA 142543-03National Institute of Allergy and Infectious Diseases 1U01AI156189-01NCATS NIH HHS UL1 TR001105NCI NIH HHS K24 CA201543NCI NIH HHS K24CA201543-01NCI NIH HHS P30 CA142543NCI NIH HHS T32 CA124334NIAID NIH HHS U01 AI156189UT Southwestern Cancer Biology Training Grant 5T32CA124334-13UT Southwestern Center for Translational Medicine UL1TR001105
6 · The paper itself

Abstract

backgroundThyroid dysfunction is among the most common autoimmune diseases and immune checkpoint inhibitor (ICI)-induced immune-related adverse events (irAE). We determined the association between longitudinal thyroid function and clinical outcomes in patients treated with ICI.

methodsWe identified all patients treated with ICI at UT Southwestern Medical Center from January 1, 2011, through December 31, 2020. We defined normal thyroid stimulating hormone (TSH) and free thyroxine (FT4) levels according to institutional reference range. We defined clinical thyroid dysfunction using established criteria incorporating labs and treatment. We determined the association between thyroid function and overall survival (OS) using Kaplan-Meier curves, log-rank tests, and multivariate Cox proportional hazards model.

resultsA total of 1781 patients were included in analyses, of whom 381 (21%) had abnormal baseline TSH. Patients with abnormal baseline TSH were more likely to be female, have kidney cancer, and initiate levothyroxine after ICI initiation (all P < 0.001). Patients with abnormal baseline TSH had inferior OS (median 16 vs 27 months; P < 0.001). Among patients with normal baseline TSH, those who had abnormal TSH after ICI initiation had improved OS (median 41 vs 22 months; P < 0.001). In a multivariate Cox model, abnormal baseline TSH was associated with worse OS (HR 1.62; 95% CI, 1.30-2.02; P < 0.001), while initiation of levothyroxine after ICI initiation was associated with improved OS (HR 0.62; 95% CI, 0.44-0.88; P = 0.008).

conclusionsICI-induced thyroid dysfunction is associated with improved survival, although abnormal TSH prior to ICI initiation is associated with inferior survival. PRECIS: Thyroid abnormalities occur commonly in the general population and as immunotherapy toxicities. We found that immunotherapy-induced thyroid dysfunction is associated with better survival, but pre-existing thyroid abnormalities convey worse outcomes.

Indexed as

Immune Checkpoint InhibitorsThyroid DiseasesFemaleHumansMalePrognosisRetrospective StudiesThyrotropinThyroxineImmune Checkpoint InhibitorsThyrotropinThyroxineAutoimmuneEndocrineImmune-related adverse eventImmunotherapyThyroid dysfunctionThyroid stimulating hormone (TSH)

Identifiers

PMID35072744
PMCPMC9308834
OpenAlexW4207018371

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.