Evidence map›Paper›PMID 38485189›Full record

Trial reportJournal for immunotherapy of cancer2024

Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Outcomes in histopathologic subgroups from the randomized, double-blind, phase 3 KEYNOTE-716 trial.

Dirk Schadendorf, Jason John Luke, Paolo A Ascierto, Georgina V Long, Piotr Rutkowski, Adnan Khattak, Michele Del Vecchio, Luis de la Cruz-Merino, Jacek Mackiewicz, Vanna Chiarion Sileni and 10 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03553836 (Adjuvant Therapy With Pembrolizumab Versus Placebo in Resected High-risk Stage II Melanoma), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 11% 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.

NCT03553836 phase3active not recruitingnot on this map

Adjuvant Therapy With Pembrolizumab Versus Placebo in Resected High-risk Stage II Melanoma: A Randomized, Double-blind Phase 3 Study (KEYNOTE-716)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2018 to 2033Enrolled976ConditionsMelanomaArmsPembrolizumab, Placebo
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. 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 at 15 institutions in 9 countries.

Dirk SchadendorfUniversity Hospital of Essen, University Duisburg-Essen, NCT-West, Essen Campus, German Cancer Consortium, Partner Site Essen & University Alliance Ruhr, One Health Research Centre, Essen, Germany dirk.schadendorf@uk-essen.de.ORCID 0000-0003-3524-7858
Jason John LukeCancer Immunotherapeutics Center, UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-1182-4908
Paolo A AsciertoMelanoma, Cancer Immunotherapy and Development Therapeutics Unit, Istituto Nazionale dei Tumori IRCCS "Fondazione G. Pascale", Naples, Italy.ORCID 0000-0002-8322-475X
Georgina V LongMelanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia.
Piotr RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0002-8920-5429
Adnan KhattakFiona Stanley Hospital, Perth, Western Australia, Australia.
Michele Del VecchioFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Luis de la Cruz-MerinoOncology Department, Virgen Macarena University Hospital; Department of Medicine, School of Medicine, University of Seville, Seville, Spain.ORCID 0000-0002-5333-0535
Jacek MackiewiczGreater Poland Cancer Center, Poznan, Poland.
Vanna Chiarion SileniMelanoma Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
John M KirkwoodUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Caroline RobertGustave Roussy and Paris-Saclay University, Villejuif, France.
Jean-Jacques GrobAix Marseille University, Hôpital de la Timone, Marseille, France.
Reinhard DummerUniversity of Zurich, Zurich, Switzerland.ORCID 0000-0002-2279-6906
Matteo S CarlinoWestmead Hospital, The University of Sydney, Melanoma Institute Australia, Sydney, New South Wales, Australia.
Yujie ZhaoMerck & Co Inc, Rahway, New Jersey, USA.ORCID 0000-0003-2896-4955
Mizuho KalabisMerck & Co Inc, Rahway, New Jersey, USA.
Clemens KreplerMerck & Co Inc, Rahway, New Jersey, USA.
Alexander EggermontUniversity Medical Centre Utrecht, Utrecht, The Netherlands.
Richard A ScolyerMelanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia.ORCID 0000-0002-8991-0013
Merck & Co., Inc., Rahway, NJ, USA (United States) · USThe University of Sydney · AUUPMC Hillman Cancer Center · USAix-Marseille Université · FREdith Cowan University · AUEssen University Hospital · DEFondazione IRCCS Istituto Nazionale dei Tumori · ITHospital Universitario Virgen Macarena · ESIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITIstituto Oncologico Veneto · ITPoznan University of Medical Sciences · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversité Paris-Saclay · FRUniversity Medical Center Utrecht · NLUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdjuvant pembrolizumab significantly improved recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) versus placebo in the phase 3 KEYNOTE-716 study of resected stage IIB or IIC melanoma. At the prespecified third interim analysis (data cut-off, January 4, 2022), the HR for RFS in the overall population was 0.64 (95% CI, 0.50 to 0.84) and the HR for DMFS was 0.64 (95% CI, 0.47 to 0.88). We present a post hoc analysis of efficacy by subtypes defined by histopathologic characteristics.

methodsPatients aged ≥12 years with newly diagnosed, resected stage IIB or IIC melanoma were randomly assigned (1:1) to pembrolizumab 200 mg every 3 weeks (2 mg/kg up to 200 mg for pediatric patients) or placebo. The primary end point was RFS per investigator review; DMFS per investigator review was secondary. Subgroups of interest were melanoma subtype (nodular vs non-nodular), tumor thickness (≤4 mm vs >4 mm), presence of ulceration (yes vs no), mitotic rate (<5 per mm

resultsBetween September 23, 2018, and November 4, 2020, 976 patients were assigned to pembrolizumab (n=487) or placebo (n=489). Median follow-up was 27.4 months (range, 14.0-39.4). The HR (95% CI) for RFS was 0.54 (0.37 to 0.79) for nodular and 0.77 (0.53 to 1.11) for non-nodular melanoma; 0.57 (0.37 to 0.89) for thickness ≤4 mm and 0.69 (0.50 to 0.96) for >4 mm; 0.66 (0.50 to 0.89) for ulceration and 0.57 (0.32 to 1.03) for no ulceration; 0.57 (0.35 to 0.92) for mitotic rate <5 per mm

conclusionsIn this post hoc analysis, the benefit of pembrolizumab was largely consistent with the overall study population regardless of histopathologic characteristics. These results support the use of adjuvant pembrolizumab in patients with resected stage IIB or IIC melanoma. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov, NCT03553836.

Indexed as

MelanomaSkin NeoplasmsAdjuvants, ImmunologicAdolescentAdultAntibodies, Monoclonal, HumanizedCombined Modality TherapyHumansAdjuvants, ImmunologicAntibodies, Monoclonal, HumanizedpembrolizumabImmune Checkpoint InhibitorsMelanomaSkin Neoplasms

Identifiers

PMID38485189
PMCPMC10941196
OpenAlexW4392820520

What OpenQuestion holds

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Registered trials

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.