Evidence map›Paper›PMID 38681767›Full record

ArticleFrontiers in endocrinology2024

Effects of immune checkpoint inhibitor associated endocrinopathies on cancer survival.

Lisa Yang, Sruthi Murthy, Alessio Cortellini, Emma A Lim, Michael Gonzalez, David J Pinato, Mariana Abdel-Malek, Sarah Mahmoud, Niamh M Martin

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

9 authors.

Lisa YangDepartment of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
Sruthi MurthyDepartment of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
Alessio CortelliniDepartment of Surgery & Cancer, Imperial College London, London, London, United Kingdom.
Emma A LimDepartment of Imaging, Imperial College Healthcare NHS Trust, London, United Kingdom.
Michael GonzalezDepartment of Medical Oncology, Imperial College Healthcare NHS Trust, London, United Kingdom.
David J PinatoDepartment of Surgery & Cancer, Imperial College London, London, London, United Kingdom.
Mariana Abdel-MalekDepartment of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
Sarah MahmoudDepartment of Pharmacy, Imperial College Healthcare NHS Trust, London, United Kingdom.
Niamh M MartinDepartment of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events (irAEs), of which endocrinopathies are common. We characterized endocrine and non-endocrine irAEs in cancer patients receiving ICIs, identified risk factors for their development and established whether endocrine and non-endocrine irAEs were differentially associated with improved cancer prognosis. Design and methods: Single-center, retrospective cohort study of patients with advanced or metastatic solid tumors receiving at least one ICI treatment cycle (242 men, 151 women, median age 65 years). Main outcome measures were incidence of any irAE during the study period, overall survival and time to treatment failure. Results: Non-endocrine irAEs occurred in 32% and endocrine irAEs in 12% of patients. Primary thyroid dysfunction was the most common endocrine irAE (9.5%) and the majority of endocrinopathies required permanent hormone replacement. Women had an increased risk of developing endocrine irAEs (p = 0.017). The biggest survival advantage occurred in patients who developed both endocrine and non-endocrine irAEs (overall survival: HR 0.16, CI 0.09-0.28). Time to treatment failure was also significantly improved in patients who developed endocrine irAEs (HR 0.49, CI 0.34 - 0.71) or both (HR 0.41, CI 0.25 - 0.64) but not in those who only developed non-endocrine irAEs. Conclusions: Women may have increased risk of endocrine irAEs secondary to ICI treatment. This is the first study to compare the effects of endocrine irAEs with non-endocrine irAEs on survival. Development of endocrine irAEs may confer survival benefit in ICI treatment and future, prospective studies are needed to elucidate this.

Indexed as

Endocrine System DiseasesImmune Checkpoint InhibitorsNeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesRisk FactorsSurvival RateImmune Checkpoint Inhibitorscancerendocrinopathyimmune checkpoint inhibitorimmune related adverse effects (irAEs)survival

Identifiers

PMID38681767
PMCPMC11045886

What Socratic holds

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LicenceCC BY
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 Socratic graph.