Evidence map›Paper›PMID 40789739›Full record

ArticleJournal for immunotherapy of cancer2025

Risk of disease progression after discontinuing immunotherapy in 105 patients with Merkel cell carcinoma who responded to PD-1 pathway blockade.

Lisa Tachiki, Yasman Moshiri, Daniel S Hippe, Emily Gong, Lauren Zawacki, Thomas Pulliam, Kristina Lachance, Candice Church, Alex Fu, Emily Huynh and 10 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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

2 citing papers in PubMed.

  1. Review
  2. 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

20 authors.

Lisa TachikiDepartment of Medicine, Division of Hematology/Oncology, University of Washington, Seattle, Washington, USA ltachiki@uw.edu.ORCID http://orcid.org/0000-0001-8057-8029
Yasman MoshiriDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Daniel S HippeClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Emily GongDepartment of Dermatology, Stanford University School of Medicine, Stanford, California, USA.ORCID http://orcid.org/0009-0009-2740-3081
Lauren ZawackiClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Thomas PulliamDepartment of Dermatology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-3511-6348
Kristina LachanceDepartment of Dermatology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0002-2697-268X
Candice ChurchDepartment of Dermatology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-1582-8292
Alex FuDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Emily HuynhDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Allison J RemingtonClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Nikhil HarikrishnanDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Marika BiermaDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Coley Doolittle-AmievaClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Tomoko AkaikeDepartment of Dermatology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-4525-6408
Song Y ParkDepartment of Dermatology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-4366-1821
Nora A AlexanderDepartment of Dermatology, University of Washington, Seattle, Washington, USA.
Lisa ZabaDepartment of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Shailender BhatiaDepartment of Medicine, Division of Hematology/Oncology, University of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0002-3816-2238
Paul T NghiemClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-2784-963X

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Jianhong Cao · 1985 to 2026
$296.4M
Understand & overcome resistance to PD-1P01CA225517 · NCI · UNIVERSITY OF WASHINGTON · PI Justin J Taylor · 2019 to 2026
$22.7M
TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
Exhaustion mechanisms in Merkel cell polyomavirus-specific T cellsF30CA254168 · NCI · UNIVERSITY OF WASHINGTON · PI PULLIAM, THOMAS · 2020 to 2023
$168k
NCI NIH HHS F30 CA254168NCI NIH HHS P01 CA225517NCI NIH HHS P30 CA015704NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) are the preferred systemic therapy for most patients with advanced Merkel cell carcinoma (MCC). However, the optimal duration of treatment for patients responding to ICI is unclear. Emerging data from retrospective analyses indicate a higher risk of MCC progression after ICI discontinuation, as compared with continuing ICI.

methodsWe performed a retrospective cohort study to evaluate the rate of progressive disease (PD) after treatment discontinuation in patients with advanced MCC who experienced objective responses to first-line ICI. We evaluated whether the risk of PD was associated with the reason for treatment discontinuation (elective vs due to toxicity) and depth of response (complete vs partial response (CR vs PR)).

resultsAmong 105 responders, 58 discontinued ICI (median treatment duration: 12 months), and 47 continued ICI (median treatment duration: 20 months) at data cut-off. With a median follow-up of 34 months from ICI initiation, 33% of the entire cohort experienced disease progression at 2 years. 2 years after ICI initiation, 39% of patients who discontinued ICI had disease progression, compared with 14% of patients who continued ICI (HR=2.34 (95% CI: 1.07 to 5.12), p=0.034). Among patients who discontinued ICI, those with PR had a numerically higher rate of progression compared with patients with CR at 2 years after ICI discontinuation (56% vs 29%, respectively; HR=1.74 (95% CI: 0.72 to 4.20), p=0.22). Patients who discontinued due to toxicity had numerically higher rates of progression at 2 years (N=28) compared with patients who discontinued electively (N=30) (45% vs 31%, respectively; HR=2.08 (95% CI: 0.79 to 5.46), p=0.14). Among responders who stayed on ICI and had not progressed by 1 year, those who electively discontinued ICI had a high chance of remaining progression-free at 2 years (89%), similar to those who continued ICI (96%, p=0.59).

conclusionsThis study highlights the high progression risk following ICI discontinuation in advanced MCC, especially among patients with non-CRs or those discontinuing early. While elective discontinuation may be appropriate after durable CRs (response≥1 year), greater caution is warranted in other settings.

Indexed as

Carcinoma, Merkel CellImmune Checkpoint InhibitorsImmunotherapyProgrammed Cell Death 1 ReceptorSkin NeoplasmsAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedRetrospective StudiesImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorComplete response - CRImmune Checkpoint InhibitorsImmunotherapyPartial responseSkin Cancer

Identifiers

PMID40789739
PMCPMC12352153

What Socratic 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 Socratic graph.