Evidence map›Paper›PMID 32860331›Full record

Trial reportCancer medicine2020

Patient-reported tolerability of veliparib combined with cisplatin and etoposide for treatment of extensive stage small cell lung cancer: Neurotoxicity and adherence data from the ECOG ACRIN cancer research group E2511 phase II randomized trial.

Laurie E Steffen McLouth, Fengmin Zhao, Taofeek K Owonikoko, Josephine L Feliciano, Nisha A Mohindra, Suzanne E Dahlberg, James L Wade, Gordan Srkalovic, Bradley W Lash, Joseph W Leach and 5 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01642251 (Phase I and Randomized Phase II Double Blind Clinical Trial of Cisplatin and Etoposide in Combination With Veliparib), which is not on this map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 30% 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.

NCT01642251 phase1 / phase2completednot on this map

Phase I and Randomized Phase II Double Blind Clinical Trial of Cisplatin and Etoposide in Combination With Veliparib (ABT-888) or Placebo as Frontline Therapy for Extensive Stage Small Cell Lung Cancer

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2012 to 2018Enrolled156ConditionsExtensive Stage Small Cell Lung Carcinoma, Large Cell Lung Carcinoma, Neuroendocrine Carcinoma, Small Cell CarcinomaArmsCisplatin, Etoposide, Veliparib, Placebo
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. 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

15 authors at 12 institutions in 1 country.

Laurie E Steffen McLouthDepartment of Behavioral Science, Center for Health Equity Transformation, University of Kentucky College of Medicine, Lexington, KY, USA.ORCID 0000-0002-4888-6520
Fengmin ZhaoDana-Farber Cancer Institute & ECOG-ACRIN Biostatistics Center, Boston, MA, USA.
Taofeek K OwonikokoEmory University, Atlanta, GA, USA.
Josephine L FelicianoJohns Hopkins University, Baltimore, MD, USA.
Nisha A MohindraNorthwestern University, Chicago, IL, USA.
Suzanne E DahlbergDana-Farber Cancer Institute & ECOG-ACRIN Biostatistics Center, Boston, MA, USA.
James L WadeHeartland NCORP, Decatur, IL, USA.
Gordan SrkalovicSparrow Herbert-Herman Cancer Center, Lansing, MI, USA.
Bradley W LashGuthrie Clinic - Robert Packer Hospital, Sayre, USA.
Joseph W LeachMetro Minnesota NCORP, Minneapolis, MN, USA.
Ticiana A LealUniversity of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Charu AggarwalUniversity of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-3181-9460
David CellaNorthwestern University, Chicago, IL, USA.
Suresh S RamalingamEmory University, Atlanta, GA, USA.
Lynne I WagnerDepartment of Social Sciences & Health Policy, Wake Forest School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0001-9685-4796
ECOG-ACRIN Cancer Research Group · USEmory University · USNorthwestern University · USHeartland Cancer Research · USJohns Hopkins University · USMetro-Minnesota Community Oncology Research Consortium · USSparrow Hospital · USSUNY Upstate Medical University · USUniversity of Kentucky · USUniversity of Pennsylvania · USUniversity of Wisconsin Carbone Cancer Center · USWake Forest University · US

Funding

ECOG-ACRIN NCORP Research Base - TMISTUG1CA189828 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$199.7M
Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$167.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO · 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
Heartland Cancer Research NCORPUG1CA189830 · NCI · DECATUR MEMORIAL HOSPITAL · PI Bryan A. Faller · 2014 to 2026
$40.9M
Michigan Cancer Research Consortium NCORPUG1CA189971 · NCI · SAINT JOSEPH MERCY HEALTH SYSTEM · PI Tareq Al baghdadi · 2014 to 2026
$36.6M
Naional Cancer Institute, Naitonal Clinical Trials Network U10 Lead Academic SiteU10CA180790 · NCI · MAYO CLINIC ROCHESTER · PI ALBERTS, STEVEN R, BOUGHEY, JUDY CAROLINE · 2014 to 2018
$6.6M
National Clinical Trials Network Research at the University of WisconsinUG1CA233277 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Lisa M Barroilhet, Andrew M. Baschnagel · 2019 to 2026
$4.9M
Postdoctoral Training Program in Cancer SurvivorshipR25CA122061 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI AVIS, NANCY E · 2008 to 2018
$3.8M
Johns Hopkins University NCTN Lead Academic Site ProgramU10CA180802 · NCI · JOHNS HOPKINS UNIVERSITY · PI ARMSTRONG, DEBORAH K, BRAHMER, JULIE RENEE · 2014 to 2018
$3.3M
Winship Cancer Institute, National Clinical Trials Network Lead Academic ParticipU10CA180864 · NCI · EMORY UNIVERSITY · PI BEITLER, JONATHAN, RAMALINGAM, SURESH S · 2014 to 2018
$2.9M
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
NCI NIH HHS R25 CA122061NCI NIH HHS T32 CA122061NCI NIH HHS U10 CA180790NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180799NCI NIH HHS U10 CA180802NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180864NCI NIH HHS UG1 CA189828NCI NIH HHS UG1 CA189830NCI NIH HHS UG1 CA189863NCI NIH HHS UG1 CA189971NCI NIH HHS UG1 CA233277
6 · The paper itself

Abstract

objectivesThe ECOG-ACRIN Cancer Research Group trial E2511 recently demonstrated a potential benefit for the addition of veliparib to cisplatin-etoposide (CE) in patients with extensive stage small cell lung cancer (ES-SCLC) in a phase II randomized controlled trial. Secondary trial endpoints included comparison of the incidence and severity of neurotoxicity, hypothesized to be lower in the veliparib arm, and tolerability of the addition of veliparib to CE. Physician-rated and patient-reported neurotoxicity was also compared. MATERIALS AND

methodsPatients randomized to veliparib plus CE (n = 64) or placebo plus CE (n = 64) completed the 11-item Functional Assessment of Cancer Therapy Gynecologic Oncology Group Neurotoxicity (questionnaire pre-treatment, end of cycle 4 [ie 3 months after randomization] and 3 months post-treatment [ie 6-months]). Adherence analysis was based on treatment forms. RESULTS AND

conclusionNo significant differences in mean or magnitude of change in neurotoxicity scores were observed between treatment arms at any time point. However, patients in the placebo arm reported worsening neurotoxicity from baseline to 3-months (M difference = -1.5, P = .045), compared to stable neurotoxicity in the veliparib arm (M difference = -0.2, P = .778). Weakness was the most common treatment-emergent (>50%) and moderate to severe (>16%) symptom reported, but did not differ between treatment arms. The proportion of adherence to oral therapy in the overall sample was 75%. Three percent of patients reported clinically significant neurotoxicity that was not captured by physician assessment. Neurotoxicity scores were not different between treatment arms. The addition of veliparib to CE appeared tolerable, though weakness should be monitored. CLINICALTRIALS. GOV IDENTIFIER: NCT01642251.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBenzimidazolesCarboplatinEtoposideFemaleHumansLung NeoplasmsMaleMedication AdherenceMiddle AgedPatient Reported Outcome MeasuresPeripheral Nervous System DiseasesSmall Cell Lung CarcinomaBenzimidazolesCarboplatinEtoposideveliparibchemotherapy-induced peripheral neuropathypatient-reported outcomessmall celltolerabilityveliparib

Identifiers

PMID32860331
PMCPMC7571824
OpenAlexW3082642899

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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.