Evidence map›Paper›PMID 32884119›Full record

ArticleScientific reports2020

Real-world analyses of therapy discontinuation of checkpoint inhibitors in metastatic melanoma patients.

Marina Amaral de Ávila Machado, Cristiano Soares de Moura, Kelvin Chan, Jeffrey R Curtis, Marie Hudson, Michal Abrahamowicz, Rahima Jamal, Louise Pilote, Sasha Bernatsky

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Comparative neurologic toxicity profiles of chemotherapy versus immune checkpoint inhibitors in melanoma: a propensity score-matched analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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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 at 6 institutions in 2 countries.

Marina Amaral de Ávila MachadoDepartment of Medicine, McGill University, Montreal, Canada.
Cristiano Soares de MouraCentre for Outcomes Research and Evaluation, Research Institute of the McGill University Health Centre, Montreal, Canada.
Kelvin ChanSunnybrook Odette Cancer Centre, University of Toronto, Toronto, ON, Canada.
Jeffrey R CurtisDepartment of Medicine, University of Alabama At Birmingham, Birmingham, USA.
Marie HudsonJewish General Hospital and Lady Davis Research Institute for Medical Research, Montreal, Canada.
Michal AbrahamowiczDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Rahima JamalCentre Hospitalier de L'Université de Montréal, Centre de Recherche du CHUM, Université de Montréal, Montreal, Canada.
Louise PiloteDepartment of Medicine, McGill University, Montreal, Canada.
Sasha BernatskyDepartment of Medicine, McGill University, Montreal, Canada. sasha.bernatsky@mcgill.ca.
McGill University · CACentre Hospitalier de l’Université de Montréal · CAJewish General Hospital · CAMcGill University Health Centre · CASunnybrook Health Science Centre · CAUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 'real-world' patient population of metastatic melanoma is not fully represented in clinical trials investigating checkpoint inhibitors. We described therapy discontinuation in an unselected population-based cohort of adults with metastatic melanoma who started therapy with pembrolizumab, nivolumab, or nivolumab/ipilimumab from January 2015 to August 2017. Therapy discontinuation was defined as a gap between doses beyond 120 days, and/or initiation of another cancer therapy. We estimated drug-specific rate ratios for therapy discontinuation adjusted for age, sex, comorbidities, health care use, and past cancer therapies. We included 876 metastatic melanoma patients initiating pembrolizumab (44.3%), nivolumab/ipilimumab (31.2%), and nivolumab (24.5%). At 12 months of follow-up, the probabilities of therapy discontinuation were 49.9% (95% confidence interval, CI 43.6-56.5) for pembrolizumab, 58.8% (95% CI 50.5-67.3) for nivolumab, and 59.2% (95% CI 51.7-66.8) for nivolumab/ipilimumab. Stratified analyses based on prior cancer therapy, brain metastases at baseline, and sex showed similar trends. In multivariable analyses, compared with pembrolizumab, patients starting nivolumab (rate ratio 1.38, 95% CI 1.08-1.77) or nivolumab/ipilimumab (rate ratio 1.30, 95% CI 1.02-1.65) were more likely to discontinue therapy. Our findings indicate frequent discontinuations of checkpoint inhibitors at one year. The lower discontinuation associated with pembrolizumab should be confirmed in further studies.

Indexed as

Withholding TreatmentAgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalFemaleHumansImmune Checkpoint InhibitorsIpilimumabMaleMelanomaMiddle AgedNivolumabSkin NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsIpilimumabNivolumabpembrolizumab

Identifiers

PMID32884119
PMCPMC7471311
OpenAlexW3082399821

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.