Evidence map›Paper›PMID 31142503›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

IL15 by Continuous Intravenous Infusion to Adult Patients with Solid Tumors in a Phase I Trial Induced Dramatic NK-Cell Subset Expansion.

Kevin C Conlon, E Lake Potter, Stefania Pittaluga, Chyi-Chia Richard Lee, Milos D Miljkovic, Thomas A Fleisher, Sigrid Dubois, Bonita R Bryant, Michael Petrus, Liyanage P Perera and 8 more

Registry-linked trialAbstract readClinical Trial, Phase I
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01572493 (A Phase I Study of a Continuous Intravenous Infusion of Recombinant Human Interleukin IL-15), which is not on this map. Cited by 93 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 1 pooled it
5.4field-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.

NCT01572493 phase1completednot on this map

A Phase I Study of a Continuous Intravenous Infusion of Recombinant Human Interleukin IL-15 (rhIL-15) in Adults With Metastatic Cancers

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2012 to 2019Enrolled38ConditionsLymphoma, CarcinomaArmsrh IL-15 (10 DAYS), rh IL-15 (5 DAYS)
3 · Its place in the literature

Who cites it

93 citing papers in PubMed, 1 synthesis or guideline pooled it, 132 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Enhanced CD56 Expression and Increased Number of CD56American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
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  11. Review
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  13. Article
  14. Natural killer cell-based immunotherapy for cancer.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Review
  15. Review
  16. Article
  17. Review
  18. Cytokines in cancer.Cancer cell · 2025
    Review
  19. Review
  20. Article

33 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

18 authors at 3 institutions in 1 country.

Kevin C ConlonLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
E Lake PotterImmunoTechnology Section Vaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland.
Stefania PittalugaLaboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Chyi-Chia Richard LeeLaboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Milos D MiljkovicLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Thomas A FleisherNIH Clinical Center, Department of Laboratory Medicine, NIH, Bethesda, Maryland.
Sigrid DuboisLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Bonita R BryantLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Michael PetrusLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Liyanage P PereraLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Jennifer HsuLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
William D FiggGenitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.ORCID 0000-0003-2428-5613
Cody J PeerGenitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Joanna H ShihBiometric Research Program, Division of Cancer Treatment and Diagnosis, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Jason L YovandichBiological Resources Branch, Division of Cancer Treatment and Diagnosis, Developmental Therapeutics Program, NCI, NIH, Frederick, Maryland.
Stephen P CreekmoreBiological Resources Branch, Division of Cancer Treatment and Diagnosis, Developmental Therapeutics Program, NCI, NIH, Frederick, Maryland.
Mario RoedererImmunoTechnology Section Vaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland.
Thomas A WaldmannLymphoid Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland. tawald@helix.nih.gov.
Center for Cancer Research · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health Clinical Center · US

Funding

Sample Processing and Analytical Methods Development for New Anticancer AgentsZICSC006536 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$18.1M
Functional And Phenotypic Characterization Of T Cells In ManZIAAI005021 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2022
$14.4M
Using Clinical Pharmacology Principles to Develop New Anticancer TherapiesZICSC006537 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$14.4M
Development Of Flow Cytometric Technologies For Immune AssaysZIAAI005020 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2019
$9.6M
Intramural NIH HHS ZIC SC006537
6 · The paper itself

Abstract

purposeThe first-in-human clinical trial with human bolus intravenous infusion IL15 (rhIL15) was limited by treatment-associated toxicity. Here, we report toxicity, immunomodulation, and clinical activity of rhIL15 administered as a 10-day continuous intravenous infusion (CIV) to patients with cancers in a phase I trial. PATIENTS AND

methodsPatients received treatment for 10 days with CIV rhIL15 in doses of 0.125, 0.25, 0.5, 1, 2, or 4 μg/kg/day. Correlative laboratory tests included IL15 pharmacokinetic (PK) analyses, and assessment of changes in lymphocyte subset numbers.

resultsTwenty-seven patients were treated with rhIL15; 2 μg/kg/day was identified as the MTD. There were eight serious adverse events including two bleeding events, papilledema, uveitis, pneumonitis, duodenal erosions, and two deaths (one due to likely drug-related gastrointestinal ischemia). Evidence of antitumor effects was observed in several patients, but stable disease was the best response noted. Patients in the 2 μg/kg/day group had a 5.8-fold increase in number of circulating CD8

conclusionsThis phase I trial identified the MTD for CIV rhIL15 and defined a treatment regimen that produced significant expansions of CD8

Indexed as

CytokinesFemaleHumansImmunohistochemistryImmunologic FactorsImmunomodulationInflammation MediatorsInfusions, IntravenousInterleukin-15Killer Cells, NaturalLymphocyte ActivationLymphocyte CountLymphocytes, Tumor-InfiltratingLymphocyte SubsetsNeoplasmsTreatment OutcomeCytokinesImmunologic FactorsInflammation MediatorsInterleukin-15

Identifiers

PMID31142503
PMCPMC6697593
OpenAlexW2946952121

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.