Evidence map›Paper›PMID 30420448›Full record

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

E3611-A Randomized Phase II Study of Ipilimumab at 3 or 10 mg/kg Alone or in Combination with High-Dose Interferon-α2b in Advanced Melanoma.

Ahmad A Tarhini, Sandra J Lee, Xiaoxue Li, Uma N M Rao, Arun Nagarajan, Mark R Albertini, Jerry W Mitchell, Stuart J Wong, Mark A Taylor, Noel Laudi and 3 more

Abstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report 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. Cited by 9 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 4 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.

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

9 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Review
  7. Neoadjuvant Pembrolizumab and High-Dose IFNα-2b in Resectable Regionally Advanced Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  8. Article
  9. Review
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

13 authors.

Ahmad A TarhiniCleveland Clinic and Case Comprehensive Cancer Center, Cleveland, Ohio. tarhina1@ccf.org.
Sandra J LeeECOG-ACRIN Biostatistics Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Xiaoxue LiDana-Farber Cancer Institute, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Uma N M RaoUniversity of Pittsburgh Cancer Institute, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Arun NagarajanCleveland Clinic Florida, Weston, Florida.
Mark R AlbertiniUniversity of Wisconsin Carbone Cancer Center, Madison, Wisconsin.ORCID 0000-0002-6499-517X
Jerry W MitchellMt. Carmel Health System, Columbus, Ohio.
Stuart J WongMedical College of Wisconsin, Milwaukee, Wisconsin.
Mark A TaylorLewis Cancer and Research Pavilion at St. Joseph's, Savannah, Georgia.
Noel LaudiMinnesota Oncology Hematology PA, Minneapolis, Minnesota.
Phu V TruongUniversity of Kansas-Wichita, Wichita, Kansas.
Robert M ConryUniversity of Alabama at Birmingham, Birmingham, Alabama.
John M KirkwoodUniversity of Pittsburgh Cancer Institute, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO, CONSTANTINE A. GATSONIS · 2014 to 2026
$111.2M
Metro-Minnesota Community Oncology Research Consortium (MMCORC)UG1CA189863 · NCI · PARK NICOLLET INSTITUTE · PI JOLEEN M HUBBARD, Yan Ji · 2014 to 2026
$43.2M
Georgia NCI Community Oncology Research Program (NCORP)UG1CA189997 · NCI · NORTHSIDE HOSPITAL ATLANTA · PI Guilherme Cantuaria, Leonard R. Henry · 2014 to 2026
$20.9M
VCU Massey Comprehensive Cancer Center NCI Community Oncology Research ProgramUG1CA189869 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI HARRY D BEAR, Khalid Matin · 2014 to 2026
$14.1M
Columbus NCORP RFA-CA-18-016UG1CA189954 · NCI · COLUMBUS COMMUNITY CLINICAL ONCOLOGY PRG · PI Aruna Gowda, Malolan S Rajagopalan · 2014 to 2026
$9.8M
NCI NCTN-Network Lead Academic Participating Site at UPMC Hillman Cancer CenterUG1CA233184 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ADAM M BRUFSKY, John Munn Kirkwood · 2019 to 2026
$7.7M
NCI NCTN-Network Lead Academic Site at UPCIU10CA180844 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BRUFSKY, ADAM M, EDWARDS, ROBERT PAGE · 2014 to 2018
$4.5M
NCTN Deep South Research ConsortiumUG1CA233330 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Charles A. Leath, Andrew M McDonald · 2019 to 2026
$3.7M
National Clinical Trials Network Research at the University of WisconsinU10CA180799 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI ANDERSON, BETHANY M, KUSHNER, DAVID M · 2014 to 2018
$2.8M
NCTN Deep South Research ConsortiumU10CA180855 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BJORNSTI, MARY-ANN, FALKSON, CARLA I · 2014 to 2018
$2.6M
NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180799NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180844NCI NIH HHS U10 CA180855NCI NIH HHS UG1 CA189863NCI NIH HHS UG1 CA189869NCI NIH HHS UG1 CA189954NCI NIH HHS UG1 CA189997NCI NIH HHS UG1 CA233184NCI NIH HHS UG1 CA233330
6 · The paper itself

Abstract

purposeInterferon-α favors a Th1 shift in immunity, and combining with ipilimumab (ipi) at 3 or 10 mg/kg may downregulate CTLA4-mediated suppressive effects, leading to more durable antitumor immune responses. A study of tremelimumab and high-dose interferon-α (HDI) showed promising efficacy, supporting this hypothesis. PATIENTS AND

methodsE3611 followed a 2-by-2 factorial design (A: ipi10+HDI; B: ipi10; C: ipi3+HDI; D: ipi3) to evaluate (i) no HDI versus HDI (across ipilimumab doses) and (ii) ipi3 versus ipi10 (across HDI status). We hypothesized that median progression-free survival (PFS) would improve from 3 to 6 months with HDI versus no HDI and with ipi10 versus ipi3.

resultsFor eligible and treated patients (

conclusionsAlthough PFS was increased, the differences resulting from adding interferon-α or a higher dose of ipilimumab did not reach statistical significance and do not outweigh the added toxicity risks.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansInterferon-alphaInterferon alpha-2IpilimumabKaplan-Meier EstimateMaleMelanomaMiddle AgedNeoplasm MetastasisNeoplasm StagingTreatment OutcomeInterferon-alphaInterferon alpha-2Interferon-alpha2bIpilimumab

Identifiers

PMID30420448
PMCPMC6335150

What OpenQuestion holds

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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.