Evidence map›Paper›PMID 39342463›Full record

Trial reportCancer2025

Southwest Oncology Group S0826: A phase 2 trial of SCH 727965 (NSC 727135, dinaciclib) in patients with stage IV melanoma.

Christopher D Lao, James Moon, Vincent T Ma, John P Fruehauf, Lawrence E Flaherty, Martin J Bury, William G Martin, Howard Gross, Wallace Akerley, Judith O Hopkins and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00937937 (A Phase II Trial of SCH 727965), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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.

NCT00937937 phase2active not recruitingnot on this map

A Phase II Trial of SCH 727965 (NSC 747135) in Patients With Stage IV Melanoma

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2009 to 2027Enrolled72ConditionsAcral Lentiginous Melanoma, Cutaneous Nodular Melanoma, Lentigo Maligna Melanoma, Low-CSD MelanomaArmsDinaciclib
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. 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

13 authors.

Christopher D LaoRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-5952-7267
James MoonSouthwest Oncology Group Statistical Center, Seattle, Washington, USA.
Vincent T MaCarbone Cancer Center, Department of Oncology, University of Wisconsin, Madison, Wisconsin, USA.ORCID https://orcid.org/0000-0002-8417-2787
John P FruehaufUniversity of California at Irvine, Orange, California, USA.
Lawrence E FlahertyBarbara Ann Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.
Martin J BuryCancer and Hematology Centers of Western Michigan, Cancer Research Consortium of West Michigan National Cancer Institute Community Research Program (NCORP), Grand Rapids, Michigan, USA.
William G MartinPacific Cancer Research Consortium NCORP, St Charles Cancer Center, Bend, Oregon, USA.
Howard GrossDayton National Cancer Institute Community Oncology Research Program, Dayton Physicians LLC-Hematology and Oncology, Dayton, Ohio, USA.
Wallace AkerleyHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Judith O HopkinsSoutheast Clinical Oncology Research Consortium NCORP, Novant Health Cancer Institute, Winston-Salem, North Carolina, USA.
Sapna P PatelUniversity of Colorado Cancer Center, Department of Medicine, University of Colorado, Aurora, Colorado, USA.
Vernon K SondakH. Lee Moffitt Cancer Center, Tampa, Florida, USA.ORCID https://orcid.org/0000-0003-1090-484X
Antoni RibasJonsson Comprehensive Cancer Center, University of California at Los Angeles, Los Angeles, California, USA.

Funding

SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Michael L. LeBlanc · 2014 to 2026
$115.2M
University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
Southeast Clinical Oncology Research Consortium, Inc. (SCOR)UG1CA189858 · NCI · SOUTHEAST CLINICAL ONCOL RES CONSORTIUM · PI Judith O Hopkins, William J Irvin · 2014 to 2026
$38.8M
Michigan Cancer Research Consortium NCORPUG1CA189971 · NCI · SAINT JOSEPH MERCY HEALTH SYSTEM · PI Tareq Al baghdadi · 2014 to 2026
$36.6M
Cancer Research Consortium of West Michigan (CRCWM)UG1CA189860 · NCI · COREWELL HEALTH · PI KATHLEEN YOST BUTLER · 2014 to 2026
$29.1M
The Pacific Cancer Research Consortium (PCRC), an NCORP Community SiteUG1CA189953 · NCI · SWEDISH MEDICAL CENTER, FIRST HILL · PI Alison Katherine Conlin, Charles Drescher · 2014 to 2026
$27.4M
Gulf South Minority/Underserved Clinical Trials Network (Gulf South M/U CTN)UG1CA189854 · NCI · LSU HEALTH SCIENCES CENTER · PI AUGUSTO C. OCHOA · 2014 to 2026
$27.1M
Dayton Clinical Oncology ProgramUG1CA189957 · NCI · DAYTON CLINICAL ONCOLOGY PROGRAM · PI Howard M Gross · 2014 to 2026
$10.7M
Next Generation Cancer Immunotherapies to Defeat MelanomaR35CA197633 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTONI RIBAS · 2015 to 2026
$10.4M
Institutional Career Development CoreKL2TR002374 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI Bo Liu, Marin Leigh Schweizer · 2017 to 2026
$9.7M
National Cancer Institute of the National Institutes of Health CA11083National Cancer Institute of the National Institutes of Health CA139519National Cancer Institute of the National Institutes of Health CA180801National Cancer Institute of the National Institutes of Health CA180818National Cancer Institute of the National Institutes of Health CA180819National Cancer Institute of the National Institutes of Health CA180834National Cancer Institute of the National Institutes of Health CA180835National Cancer Institute of the National Institutes of Health CA180888National Cancer Institute of the National Institutes of Health CA189817National Cancer Institute of the National Institutes of Health CA189853National Cancer Institute of the National Institutes of Health CA189854National Cancer Institute of the National Institutes of Health CA189858National Cancer Institute of the National Institutes of Health CA189860National Cancer Institute of the National Institutes of Health CA189953National Cancer Institute of the National Institutes of Health CA189957National Cancer Institute of the National Institutes of Health CA189971National Cancer Institute of the National Institutes of Health CA35128National Cancer Institute of the National Institutes of Health CA46282NCATS NIH HHS KL2 TR002374NCATS NIH HHS UL1 TR002373NCI NIH HHS P30 CA016042NCI NIH HHS R35 CA197633NCI NIH HHS U10 CA011083NCI NIH HHS U10 CA035128NCI NIH HHS U10 CA046282NCI NIH HHS U10 CA139519NCI NIH HHS U10 CA180801NCI NIH HHS U10 CA180818NCI NIH HHS U10 CA180819NCI NIH HHS U10 CA180834NCI NIH HHS U10 CA180835NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA189817NCI NIH HHS UG1 CA189853NCI NIH HHS UG1 CA189854NCI NIH HHS UG1 CA189858NCI NIH HHS UG1 CA189860NCI NIH HHS UG1 CA189953NCI NIH HHS UG1 CA189957NCI NIH HHS UG1 CA189971NCI NIH HHS UG1 CA233160
6 · The paper itself

Abstract

backgroundCell cycle inhibition is an established therapeutic approach for some cancers. A multicenter, single-arm, phase 2 trial (ClinicalTrials.gov identifier NCT00937937) of the cyclin-dependent kinase inhibitor SCH 727965 (NSC 747135; dinaciclib) was conducted in patients with metastatic melanoma to determine its clinical activity.

methodsPatients with metastatic melanoma of cutaneous or mucosal origin were eligible if they had zero to one previous treatments, a Zubrod performance status of 0-1, and adequate organ function. SCH 727965 50 mg/m

resultsSeventy-two patients were enrolled from July 1, 2009, to November 1, 2010, at 24 institutions. Sixty-eight percent of patients had M1c disease, and 43% had elevated lactate dehydrogenase levels. Twenty-eight patients (39%) experienced grade 4 adverse events, including 20 cases of neutropenia. Sixty-seven patients were evaluable for response. There was a response in zero of 67 patients (95% confidence interval [CI], 0%-5%), and stable disease was observed in 21%. The estimated median PFS was 1.4 months (95% CI, 1.4-1.5 months), and the 6-month PFS rate was 6% (2%-13%). The median OS was 8.2 months (95% CI, 5.5-10.5 months), and the 1-year OS rate was 38% (95% CI, 26%-49%).

conclusionsThis multicenter, US National Cancer Institute Cancer Therapy Evaluation Program-sponsored trial of SCH 727965 was conducted at a time when the current generation of effective therapies for melanoma were not available. Although the null hypothesis of 1-year OS was rejected, the minimal PFS impact and substantive toxicity indicated that this regimen lacks justification for further investigation as a single agent.

Indexed as

Cyclic N-OxidesIndolizinesMelanomaNeoplasm StagingPyridinium CompoundsAdultAgedAged, 80 and overBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedProgression-Free SurvivalSkin NeoplasmsBridged Bicyclo Compounds, HeterocyclicCyclic N-OxidesdinaciclibIndolizinesPyridinium CompoundsCDK inhibitioncyclin‐dependent kinase (CDK)dinaciclibmelanoma

Identifiers

PMID39342463
PMCPMC11694162

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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.