Evidence map›Paper›PMID 33500258›Full record

Observational studyJournal for immunotherapy of cancer2021

Real-world experience with elective discontinuation of PD-1 inhibitors at 1 year in patients with metastatic melanoma.

Rebecca Pokorny, Jordan P McPherson, Benjamin Haaland, Kenneth F Grossmann, Carolyn Luckett, Benjamin Newell Voorhies, Daniel S Sageser, Jocelyn Wallentine, Zachary Tolman, Siwen Hu-Lieskovan and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal for immunotherapy of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Survival after cessation of immunotherapies in melanoma: A systematic review and meta-analysis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
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  13. Real-world management of patients with complete response under immune-checkpoint inhibition for advanced melanoma.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025
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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

11 authors at 2 institutions in 1 country.

Rebecca PokornyDepartment of Pharmacy, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Jordan P McPhersonDepartment of Pharmacy, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Benjamin HaalandDivision of Oncology and Department of Population Health Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Kenneth F GrossmannDepartment of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Carolyn LuckettDepartment of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Benjamin Newell VoorhiesDivision of Oncology, Department of Medicine, Intermountain Healthcare, Salt Lake City, Utah, USA.
Daniel S SageserDepartment of Pharmacy, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Jocelyn WallentineDepartment of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Zachary TolmanDepartment of Pharmacy, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Siwen Hu-LieskovanDepartment of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Umang SwamiDepartment of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA umang.swami@hci.utah.edu.ORCID 0000-0003-3518-0411
University of Utah · USIntermountain Healthcare · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
NCATS NIH HHS UL1 TR002538NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

backgroundRandomized trials evaluating programmed cell death protein 1 (PD-1) inhibitors in metastatic melanoma either permitted treatment for 2 years (pembrolizumab) or more (nivolumab). The optimal duration of therapy is currently unknown due to limited data, and shorter therapies may be effective.

methodsData of patients with metastatic cutaneous melanoma treated with single-agent PD-1 inhibitors at Huntsman Cancer Institute from January 1, 2015, to December 31, 2018, was reviewed to identify a continuous series of patients who made the joint decision with their provider to electively discontinue therapy at 1 year (>6 months and <18 months) in the setting of ongoing treatment response or disease stability. Patients were excluded if they received PD-1 inhibitors with other systemic therapy, had prior exposure to PD-1 therapy, or discontinued treatment due to disease progression or immune-related adverse event. Best objective response (BOR) per RECIST V.1.1 at treatment discontinuation, progression-free survival (PFS), and retreatment characteristics was analyzed.

resultsOf 480 patients who received PD-1 inhibitors, 52 met the inclusion criteria. The median treatment duration from first to the last dose was 11.1 months (95% CI 10.5 to 11.4). BOR was complete response in 13 (25%), partial response in 28 (53.8%), and stable disease in 11 (21.2%) patients. After a median follow-up of 20.5 months (range 3-49.2) from treatment discontinuation, 39 (75%) patients remained without disease progression, while 13 (25%) had progression (median PFS 3.9 months; range 0.7-30.9). On multivariable analysis, younger age, history of brain metastasis, and higher lactate dehydrogenase at the time of anti-PD-1 discontinuation were associated with recurrence. Patients with recurrent melanoma were managed with localized treatment, anti-PD-1 therapies, and BRAF-MEK inhibitors. All patients except one were alive at data cutoff.

conclusionIn this large real-world, observational cohort study, the majority of patients with metastatic melanoma after 1 year of anti-PD-1 therapy remained without progression on long-term follow-up. The risk of disease progression even in patients with residual disease on imaging was low. After prospective validation, elective PD-1 discontinuation at 1 year may reduce financial and immunotherapy-related toxicity without sacrificing outcomes.

Indexed as

AdultAgedAged, 80 and overCutaneous Malignant MelanomaDecision Making, SharedFemaleHumansImmune Checkpoint InhibitorsMaleMelanomaMiddle AgedNeoplasm MetastasisProgrammed Cell Death 1 ReceptorResponse Evaluation Criteria in Solid TumorsRisk AssessmentSkin NeoplasmsImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorimmunotherapymelanoma

Identifiers

PMID33500258
PMCPMC7843310
OpenAlexW3121649431

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.