Evidence map›Paper›PMID 28838379›Full record

Trial reportLung cancer (Amsterdam, Netherlands)2017

Phase II study of olaratumab with paclitaxel/carboplatin (P/C) or P/C alone in previously untreated advanced NSCLC.

David E Gerber, Paul Swanson, Ariel Lopez-Chavez, Lucas Wong, Afshin Dowlati, Nathan A Pennell, Damien M Cronier, Amy Qin, Robert Ilaria, Jan Cosaert and 2 more

3 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Lung cancer (Amsterdam, Netherlands), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 16% 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.

NCT02677116 phase1completednot on this map

A Phase 1, Open-Label, Dose-Escalation Study of Olaratumab as a Single Agent and in Combination With Doxorubicin, Vincristine/Irinotecan, or High-Dose Ifosfamide in Pediatric Patients With Relapsed or Refractory Solid Tumors

TypeinterventionalSponsorEli Lilly and CompanyRan2016 to 2019Enrolled68ConditionsNeoplasm MetastasisArmsOlaratumab, Doxorubicin, Vincristine, Irinotecan, Ifosfamide
NCT02783599 phase1completednot on this map

A Phase 1b Trial to Assess the Modulation of Biological Markers in Patients With Potentially Resectable Soft Tissue Sarcoma Treated With Olaratumab Monotherapy Followed by Olaratumab Plus Doxorubicin Combination Therapy

TypeinterventionalSponsorEli Lilly and CompanyRan2016 to 2018Enrolled51ConditionsSoft Tissue SarcomaArmsOlaratumab, Doxorubicin, External Beam Radiotherapy
NCT03086369 phase1 / phase2completednot on this map

A Phase 1b (Open-Label) / Phase 2 (Randomized, Double-Blinded) Study Evaluating Nab-Paclitaxel and Gemcitabine With or Without Olaratumab in the Treatment of First-Line Metastatic Pancreatic Cancer

TypeinterventionalSponsorEli Lilly and CompanyRan2017 to 2021Enrolled184ConditionsMetastatic Pancreatic CancerArmsOlaratumab, Nab-paclitaxel, Gemcitabine, Placebo
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

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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 9 institutions in 3 countries.

David E GerberThe University of Texas, Southwestern Medical Center at Dallas, Harry Hines Blvd., Mail Code 8852, Dallas, TX 75390-8852, USA. Electronic address: david.gerber@utsouthwestern.edu.
Paul SwansonHematology/Oncology Associates of the Treasure Coast, Port Saint Lucie, FL 34952, USA. Electronic address: paulmswanson@msn.com.
Ariel Lopez-ChavezOregon Health and Science University, Portland, OR 97239, USA. Electronic address: lopezcha@ohsu.edu.
Lucas WongScott & White Clinic, Hematology-Oncology, Temple, TX 76508, USA. Electronic address: lwong@sw.org.
Afshin DowlatiCase Western Reserve University, Cleveland, OH 44106, USA. Electronic address: afshin.dowlati@case.edu.
Nathan A PennellCleveland Clinic, Cleveland, OH 44195, USA. Electronic address: penneln@ccf.org.
Damien M CronierEli Lilly and Company, Windlesham GU20 6PH, UK. Electronic address: cronier_damien@lilly.com.
Amy QinEli Lilly and Company, Bridgewater, NJ 08807, USA. Electronic address: amy.qin@lilly.com.
Robert IlariaEli Lilly and Company, Indianapolis, IN 46285, USA. Electronic address: Ilaria_robert_l@lilly.com.
Jan CosaertSotio a.s., 170 00 Prague 7, Czech Republic. Electronic address: jan.cosaert2@gmail.com.
Ashwin ShahirEli Lilly and Company, United Kingdom of Great Britain and Northern Ireland, UK.
Maria Q BaggstromWashington University, St. Louis, MO 63130, USA. Electronic address: mbaggstr@dom.wustl.edu.
Eli Lilly (United Kingdom) · GBEli Lilly (United States) · USCase Western Reserve University · USCleveland Clinic · USHematology Oncology Associates · USOregon Health & Science University · USSotio (Czechia) · CZThe University of Texas Southwestern Medical Center · USWashington University in St. Louis · US

Funding

Development of New Cancer Treatments and InvestigatorsK24CA201543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC · 2016 to 2020
$737k
NCI NIH HHS K24 CA201543
6 · The paper itself

Abstract

backgroundIn non-small cell lung cancer (NSCLC), platelet-derived growth factor receptor (PDGFR) mediates angiogenesis, tissue invasion, and tumor interstitial pressure. Olaratumab (IMC-3G3) is a fully human anti-PDGFRα monoclonal antibody. This Phase II study assessed safety and efficacy of olaratumab+paclitaxel/carboplatin (P/C) versus P/C alone for previously untreated advanced NSCLC. MATERIALS AND

methodsPatients received up to six 21-day cycles of P 200mg/m

results131 patients were: 67 with olaratumab+P/C and 64 with P/C; 74% had nonsquamous NSCLC. Median PFS was similar between olaratumab+P/C and P/C (4.4 months each) (HR 1.29; 95% CI [0.86-1.93]; p=0.21). Median OS was similar between olaratumab+P/C (11.8 months) and P/C (11.5 months) (HR 1.04; 95% CI [0.68-1.57]; p=0.87). Both arms had similar toxicity profiles. All evaluable cases were PDGFR-negative by immunohistochemistry. Tumor stroma PDGFR expression was evaluable in 23/131 patients, of which 78% were positive.

conclusionsThe addition of olaratumab to P/C did not result in significant prolongation of PFS or OS in advanced NSCLC. Olaratumab studies in other patient populations, including soft tissue sarcoma (NCT02783599), pancreatic cancer (NCT03086369), and pediatric malignancies (NCT02677116) are underway.

Indexed as

AgedAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungCombined Modality TherapyDrug Administration ScheduleFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingPaclitaxelRemission InductionSurvival AnalysisTreatment OutcomeAntibodies, MonoclonalolaratumabPaclitaxelNSCLCOlaratumabPaclitaxel/carboplatinPDGFR

Identifiers

PMID28838379
PMCPMC5672830
OpenAlexW2738263035

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.