Evidence map›Paper›PMID 30715153›Full record

Trial reportAnnals of oncology : official journal of the European Society for Medical Oncology2019

Five-year survival outcomes for patients with advanced melanoma treated with pembrolizumab in KEYNOTE-001.

O Hamid, C Robert, A Daud, F S Hodi, W J Hwu, R Kefford, J D Wolchok, P Hersey, R Joseph, J S Weber and 10 more

2 registry-linked trialsAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Annals of oncology : official journal of the European Society for Medical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 569 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
569citing papers in PubMed, 8 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.

NCT01295827 phase1completednot on this map

Phase I Study of Single Agent Pembrolizumab (MK-3475) in Patients With Progressive Locally Advanced or Metastatic Carcinoma, Melanoma, and Non-Small Cell Lung Carcinoma (KEYNOTE 001)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2011 to 2018Enrolled1,260ConditionsCancer, Solid TumorArmsPembrolizumab
NCT06125223 not yet recruitingnot on this mapstarted 2023, after this paper: background citation

A Single-arm, Prospective, Phase II Study of PABLIXIMAB Combined With TP Chemotherapy as Neoadjuvant Therapy for Locally Advanced Head and Neck Squamous-cell Carcinoma

TypeobservationalSponsorXijing HospitalRan2023 to 2026Enrolled45ConditionsSquamous Cell Carcinoma of Head and Neck, Neoadjuvant Therapy, Immunotherapy
3 · Its place in the literature

Who cites it

569 citing papers in PubMed, 8 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Survival after cessation of immunotherapies in melanoma: A systematic review and meta-analysis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Pooled it
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  5. Biological Sample Collection to Advance Research and Treatment: A Fight Osteosarcoma Through European Research and Euro Ewing Consortium Statement.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Guideline
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  9. Trial
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  14. Review
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  19. Adaptive resistance in cancer immunotherapy.Cellular & molecular immunology · 2026
    Review
  20. Article

509 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

O HamidMedical Oncology, The Angeles Clinic and Research Institute, Los Angeles, USA. Electronic address: ohamid@theangelesclinic.org.
C RobertDepartment of Dermatology, Gustave Roussy, Villejuif; Department of Medicine, University of Paris-Sud, Paris, France.
A DaudDepartment of Medicine, University of California, San Francisco, San Francisco.
F S HodiMedical Oncology, Dana-Farber Cancer Institute, Boston.
W J HwuDepartment of Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA.
R KeffordMedical Oncology, Westmead Hospital, Westmead; Medical Oncology, Melanoma Institute Australia, Sydney; Medical Oncology, Macquarie University, Macquarie Park; Medical Oncology, University of Sydney, Sydney, Australia.
J D WolchokDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.
P HerseyMedical Oncology, University of Sydney, Sydney, Australia; Department of Medicine, Centenary Institute, Sydney, Australia.
R JosephMedical Oncology, Mayo Clinic Cancer Center-Florida, Jacksonville.
J S WeberDepartment of Medicine, Perlmutter Cancer Center, NYU Langone Health, New York.
R DroncaMedical Oncology, Mayo Clinic Cancer Center-Florida, Jacksonville.
T C MitchellDivision of Hematology Oncology, Abramson Cancer Center, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia.
A PatnaikMedical Oncology, South Texas Accelerated Research Therapeutics, San Antonio.
H M ZarourDepartment of Immunology, University of Pittsburgh Cancer Institute, Pittsburgh, USA.
A M JoshuaMedical Oncology, Melanoma Institute Australia, Sydney; Medical Oncology, University of Sydney, Sydney, Australia; Kinghorn Cancer Centre, St. Vincent's Hospital, Medical Oncology, Garvan Institute of Medical Research, Sydney; Medical Oncology, University of New South Wales, Sydney, Australia.
Q ZhaoMerck & Co., Inc., Kenilworth.
E JensenMerck & Co., Inc., Kenilworth.
S AhsanMerck & Co., Inc., Kenilworth.
N IbrahimMerck & Co., Inc., Kenilworth.
A RibasDepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundPembrolizumab demonstrated robust antitumor activity and safety in the phase Ib KEYNOTE-001 study (NCT01295827) of advanced melanoma. Five-year outcomes in all patients and treatment-naive patients are reported herein. Patients whose disease progressed following initial response and who received a second course of pembrolizumab were also analyzed. PATIENTS AND

methodsPatients aged ≥18 years with previously treated or treatment-naive advanced/metastatic melanoma received pembrolizumab 2 mg/kg every 3 weeks, 10 mg/kg every 3 weeks, or 10 mg/kg every 2 weeks until disease progression, intolerable toxicity, or patient/investigator decision to withdraw. Kaplan-Meier estimates of overall survival (OS) and progression-free survival (PFS) were calculated. Objective response rate and PFS were based on immune-related response criteria by investigator assessment (data cut-off, September 1, 2017).

resultsKEYNOTE-001 enrolled 655 patients with melanoma; median follow-up was 55 months. Estimated 5-year OS was 34% in all patients and 41% in treatment-naive patients; median OS was 23.8 months (95% CI, 20.2-30.4) and 38.6 months (95% CI, 27.2-not reached), respectively. Estimated 5-year PFS rates were 21% in all patients and 29% in treatment-naive patients; median PFS was 8.3 months (95% CI, 5.8-11.1) and 16.9 months (95% CI, 9.3-35.5), respectively. Median response duration was not reached; 73% of all responses and 82% of treatment-naive responses were ongoing at data cut-off; the longest response was ongoing at 66 months. Four patients [all with prior response of complete response (CR)] whose disease progressed during observation subsequently received second-course pembrolizumab. One patient each achieved CR and partial response (after data cut-off). Treatment-related AEs (TRAEs) occurred in 86% of patients and resulted in study discontinuation in 7.8%; 17% experienced grade 3/4 TRAE.

conclusionsThis 5-year analysis of KEYNOTE-001 represents the longest follow-up for pembrolizumab to date and confirms the durable antitumor activity and tolerability of pembrolizumab in advanced melanoma. CLINICAL TRIAL REGISTRY: ClinicalTrials.gov, NCT01295827.

Indexed as

AdultAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDrug Administration ScheduleFollow-Up StudiesHumansKaplan-Meier EstimateMelanomaResponse Evaluation Criteria in Solid TumorsSkin NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumablong-term follow-upmelanomametastaticoverall survivalpembrolizumabtreatment-naive

Identifiers

PMID30715153
PMCPMC6503622

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.