Evidence map›Paper›PMID 33646489›Full record

ArticleInvestigational new drugs2021

Phase IB study of sorafenib and evofosfamide in patients with advanced hepatocellular and renal cell carcinomas (NCCTG N1135, Alliance).

Nguyen H Tran, Nathan R Foster, Amit Mahipal, Thomas Byrne, Joleen Hubbard, Alvin Silva, Kabir Mody, Steven Alberts, Mitesh J Borad

Open access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Nitroaromatic Hypoxia-Activated Prodrugs for Cancer Therapy.Pharmaceuticals (Basel, Switzerland) · 2022
    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

9 authors at 6 institutions in 1 country.

Nguyen H TranDivision of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Nathan R FosterAlliance Statistics and Data Center, Mayo Clinic, Rochester, MN, USA.
Amit MahipalDivision of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Thomas ByrneDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ, USA.
Joleen HubbardDivision of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Alvin SilvaDepartment of Radiology, Mayo Clinic, AZ, Scottsdale, USA.
Kabir ModyDivision of Oncology, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Steven AlbertsDivision of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Mitesh J BoradMayo Clinic Cancer Center, Mayo Clinic, Phoenix, AZ, USA. borad.mitesh@mayo.edu.
Mayo Clinic in Arizona · USMayo Clinic · USAlliance Data (United States) · USJacksonville College · USMayo Clinic in Florida · USWinnMed · US

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
NCI, National Clinical Trials Network Lead Academic Participating Site (LAPS) UG1 (funded extension)UG1CA232760 · NCI · MAYO CLINIC ROCHESTER · PI Judy Caroline Boughey, Aaron Scott Mansfield · 2019 to 2026
$8.5M
Oncolytic Virotherapy in Hepatocellular CancerDP2CA195764 · NCI · MAYO CLINIC ARIZONA · PI BORAD, MITESH · 2014 to 2016
$2.7M
NCI NIH HHS DP2 CA195764NCI NIH HHS K12 CA090628NCI NIH HHS P30 CA015083NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233180
6 · The paper itself

Abstract

Background Sorafenib (Sor) remains a first-line option for hepatocellular carcinoma (HCC) or refractory renal cell carcinomas (RCC). PLC/PRF/5 HCC model showed upregulation of hypoxia with enhanced efficacy when Sor is combined with hypoxia-activated prodrug evofosfamide (Evo). Methods This phase IB 3 + 3 design investigated 3 Evo dose levels (240, 340, 480 mg/m

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularCarcinoma, Renal CellFemaleHumansKidney NeoplasmsLiver NeoplasmsMaleMaximum Tolerated DoseMiddle AgedNitroimidazolesPhosphoramide MustardsSorafenibTreatment OutcomeNitroimidazolesPhosphoramide MustardsSorafenibTH 302EvofosfamideHepatocellular cancerHypoxia activated pro-drug (HAP)

Identifiers

PMID33646489
PMCPMC8282689
OpenAlexW3135596333

What OpenQuestion holds

Textmetadata
LicenceTDM
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.