Evidence map›Paper›PMID 25649350›Full record

Trial reportCancer immunology research2015

Survivorship in Immune Therapy: Assessing Chronic Immune Toxicities, Health Outcomes, and Functional Status among Long-term Ipilimumab Survivors at a Single Referral Center.

Douglas B Johnson, Debra L Friedman, Elizabeth Berry, Ilka Decker, Fei Ye, Shilin Zhao, Alicia K Morgans, Igor Puzanov, Jeffrey A Sosman, Christine M Lovly

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Cancer immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
5.2field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
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  13. Article
  14. Review
  15. Review
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  17. Review
  18. Endocrine toxicities of immune checkpoint inhibitors.Nature reviews. Endocrinology · 2021
    Review
  19. The dark side of immunotherapy.Annals of translational medicine · 2021
    Review
  20. 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

10 authors at 1 institution in 1 country.

Douglas B JohnsonDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee. douglas.b.johnson@vanderbilt.edu.
Debra L FriedmanDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
Elizabeth BerryDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Ilka DeckerDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Fei YeDepartment of Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Shilin ZhaoDepartment of Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Alicia K MorgansDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Igor PuzanovDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Jeffrey A SosmanDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Christine M LovlyDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee. Department of Cancer Biology, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt University Medical Center · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
NCATS NIH HHS UL1 TR000445NCI NIH HHS K12 CA090625NCI NIH HHS K12 CA 0906525
6 · The paper itself

Abstract

Ipilimumab, a novel immune checkpoint inhibitor, is associated with long-term survival in approximately 20% of patients with advanced melanoma and is also being evaluated in the adjuvant setting. With this growing cohort of survivors, long-term health outcomes, chronic toxicities, and functional outcomes among survivors treated with ipilimumab need to be defined. Using retrospective medical record abstraction, we evaluated disease status, chronic immune- and non-immune-related health events, pharmacologic management of symptoms, and functional status in patients with melanoma, with overall survival ≥2 years following ipilimumab treatment at Vanderbilt University. Ninety patients received ipilimumab for metastatic disease or as adjuvant therapy between January 2006 and September 2012, and 33 patients survived ≥2 years, with a median overall survival of 60.1 months. Of these, 24 patients were alive at the last follow-up (73%), with 14 patients free of disease (42%). Gastrointestinal and dermatologic adverse events were frequent but largely transient. By contrast, patients with hypophysitis universally required ongoing corticosteroids, although largely remained asymptomatic with appropriate hormone replacement. Surviving patients generally had excellent performance status (ECOG 0-1 in 23 of 24). Chronic neurologic toxicities caused substantial morbidity and mortality in 2 patients who received whole-brain radiotherapy >5 years before analysis, and in one patient with chronic, painful peripheral neuropathy. No previously undescribed cardiac, pulmonary, gastrointestinal, hematologic, or neoplastic safety signals were identified. In conclusion, ipilimumab was associated with largely excellent functional outcomes among long-term survivors. Chronic endocrine dysfunction and occasional neurologic toxicity (primarily associated with whole-brain radiation) were observed in a small number of patients.

Indexed as

Antibodies, MonoclonalAntineoplastic AgentsColitisDiarrheaDisease-Free SurvivalExanthemaHumansImmunotherapyIpilimumabMelanomaNeuralgiaPituitary DiseasesPruritusTreatment OutcomeAntibodies, MonoclonalAntineoplastic AgentsIpilimumab

Identifiers

PMID25649350
PMCPMC4420706
OpenAlexW2154441168

What OpenQuestion holds

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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.