Evidence map›Paper›PMID 23772560›Full record

ReviewAnnals of the New York Academy of Sciences2013

Development of ipilimumab: a novel immunotherapeutic approach for the treatment of advanced melanoma.

Jedd D Wolchok, F Stephen Hodi, Jeffrey S Weber, James P Allison, Walter J Urba, Caroline Robert, Steven J O'Day, Axel Hoos, Rachel Humphrey, David M Berman and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 2 pooled it
18.4field-weighted citation impact, top 1% 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

161 citing papers in PubMed, 2 syntheses or guidelines pooled it, 306 citations in OpenAlex.

  1. Pooled it
  2. Radical multimodality therapy for malignant pleural mesothelioma.The Cochrane database of systematic reviews · 2018
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Survival follow-up and ipilimumab retreatment of patients with advanced melanoma who received ipilimumab in prior phase II studies.Annals of oncology : official journal of the European Society for Medical Oncology · 2014
    Trial
  8. Trial
  9. Review
  10. Review
  11. Review
  12. [Molecular imaging and biology · 2025
    Article
  13. Review
  14. Review
  15. One Step Ahead: Preventing Tumor Adaptation to Immune Therapy.American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2025
    Review
  16. Review
  17. Review
  18. Immune checkpoint inhibitor-associated myocarditis: a historical and comprehensive review.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  19. Article
  20. Article

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

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

12 authors at 11 institutions in 5 countries.

Jedd D WolchokMemorial Sloan-Kettering Cancer Center, New York, New York 10021, USA. wolchokj@mskcc.org
F Stephen Hodi
Jeffrey S Weber
James P Allison
Walter J Urba
Caroline Robert
Steven J O'Day
Axel Hoos
Rachel Humphrey
David M Berman
Nils Lonberg
Alan J Korman
Bristol-Myers Squibb (Germany) · DEBeverly Hills Cancer Center · USBristol-Myers Squibb (United States) · USDana-Farber Cancer Institute · USGlaxoSmithKline (United States) · USInstitut Gustave Roussy · FRMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USProvidence Portland Medical Center · USPyrogenesis (Canada) · CAThe University of Texas MD Anderson Cancer Center · US

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

The immunotherapeutic agent ipilimumab has helped address a significant unmet need in the treatment of advanced melanoma. Ipilimumab is a fully human monoclonal antibody that targets cytotoxic T-lymphocyte antigen-4 (CTLA-4), thereby augmenting antitumor immune responses. After decades in which a number of clinical trials were conducted, ipilimumab was the first therapy to improve overall survival in a randomized, controlled phase III trial of patients with advanced melanoma. These results led to the regulatory approval of ipilimumab at 3 mg/kg for the treatment of unresectable or metastatic melanoma. More than 17,000 patients worldwide have received ipilimumab, either as a commercial drug at 3 mg/kg or in clinical trials and expanded access programs at different doses. Consistent with its proposed mechanism of action, the most common toxicities associated with ipilimumab therapy are inflammatory in nature. These immune-related adverse events were mostly reversible when effective treatment guidelines were followed. Importantly, long-term follow-up of patients who received ipilimumab in a phase III trial showed that 24% survived at least two years, and in phase II studies, a proportion of patients survived at least five years. Evaluation of ipilimumab is ongoing in the adjuvant setting for melanoma, and for advanced disease in nonsmall cell lung, small cell lung, prostate, ovarian, and gastric cancers.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsClinical Trials as TopicHumansImmunotherapyIpilimumabMelanomaSkin NeoplasmsSurvival RateTreatment OutcomeAntibodies, MonoclonalAntineoplastic AgentsIpilimumabcytotoxic T-lymphocyte antigen-4immuno-oncologyimmunotherapyipilimumabmelanomamonoclonal antibody

Identifiers

PMID23772560
PMCPMC3910157
OpenAlexW2111877246

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.