Evidence map›Paper›PMID 31821732›Full record

Trial reportCancer medicine2020

Pharmacokinetics of doxorubicin following concomitant intravenous administration of olaratumab (IMC-3G3) to patients with advanced soft tissue sarcoma.

Victor M Villalobos, Gary Mo, Mark Agulnik, Seth M Pollack, Daniel A Rushing, Arun Singh, Brian A Van Tine, Rhian McNaughton, Rodney L Decker, Wei Zhang and 2 more

Open access · goldAbstract readClinical Trial, Phase IRandomized 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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Development of a First-in-Class Click Chemistry-Based Cancer Therapeutic, from Preclinical Evaluation to a First-in-Human Dose Escalation Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    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

12 authors at 8 institutions in 2 countries.

Victor M VillalobosUniversity of Colorado Denver, Anschutz Medical Campus, Aurora, CO, USA.
Gary MoEli Lilly and Company, Indianapolis, IN, USA.
Mark AgulnikDivision of Hematology/Oncology, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Seth M PollackDivision of Oncology, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA, USA.
Daniel A RushingSimon Cancer Center Indiana University Medical Center, Indianapolis, IN, USA.
Arun SinghDivision of Hematology-Oncology, University of California, Los Angeles, CA, USA.
Brian A Van TineDivision of Medical Oncology, Department of Internal Medicine, Siteman Cancer Center, St. Louis School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-4572-6668
Rhian McNaughtonEli Lilly and Company, Windlesham, Surrey, UK.
Rodney L DeckerEli Lilly and Company, Indianapolis, IN, USA.
Wei ZhangEli Lilly and Company, Indianapolis, IN, USA.
Ashwin ShahirEli Lilly and Company, Windlesham, Surrey, UK.
Damien M CronierEli Lilly and Company, Indianapolis, IN, USA.
Eli Lilly (United States) · USEli Lilly (United Kingdom) · GBIndiana University Health · USNorthwestern University · USSt. Louis VA Medical Center · USUniversity of California, Los Angeles · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOlaratumab, a fully human monoclonal antibody, selectively binds to human platelet-derived growth factor receptor alpha and blocks ligand binding. This study assessed the effect of olaratumab on the pharmacokinetics (PK) of doxorubicin and the safety of olaratumab alone and in combination with doxorubicin.

methodsThis open-label randomized phase 1 trial enrolled 49 patients ages 27 to 83 with metastatic or locally advanced soft tissue sarcoma (STS). Patients participated in 21-day treatment cycles (up to 8) until they met discontinuation criteria. In cycles 1 and 2, patients received olaratumab (15 mg/kg in Part A, 20 mg/kg in Part B) and doxorubicin (75 mg/m

resultsPK properties of doxorubicin administered alone or in combination with olaratumab (15 or 20 mg/kg) were similar for AUC(0-t

conclusionsOlaratumab at 15 or 20 mg/kg before doxorubicin infusion had no clinically relevant effect on systemic exposure to doxorubicin compared with doxorubicin alone in patients with metastatic or locally advanced STS.

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsDisease ProgressionDoxorubicinDrug InteractionsFemaleHumansInfusions, IntravenousMaleMiddle AgedNeoplasm StagingSarcomaAntibodies, MonoclonalDoxorubicinolaratumabdoxorubicinmonoclonal antibodyolaratumabpharmacokineticssoft tissue sarcoma

Identifiers

PMID31821732
PMCPMC6997100
OpenAlexW2995188062

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.