Evidence map›Paper›PMID 28744667›Full record

ArticleCancer chemotherapy and pharmacology2017

Exposure-response relationship of ramucirumab in patients with advanced second-line colorectal cancer: exploratory analysis of the RAISE trial.

Allen Lee Cohn, Takayuki Yoshino, Volker Heinemann, Radka Obermannova, György Bodoky, Jana Prausová, Rocio Garcia-Carbonero, Tudor Ciuleanu, Pilar Garcia-Alfonso, David C Portnoy and 11 more

Abstract read
In one paragraph

Article in Cancer chemotherapy and pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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.

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

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

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
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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

21 authors.

Allen Lee CohnRocky Mountain Cancer Center, 1800 Williams Street, Denver, CO, 80218, USA. allen.cohn@usoncology.com.
Takayuki YoshinoNational Cancer Center Hospital East, Chiba, Japan.
Volker HeinemannLudwig-Maximilians-University Hospital Munich, Munich, Germany.
Radka ObermannovaMasaryk Memorial Cancer Institute, Brno, Czech Republic.
György BodokySzent László Hospital, Budapest, Hungary.
Jana PrausováUniversity Hospital Motol, Prague, Czech Republic.
Rocio Garcia-CarboneroHospital Virgen del Rocio, Seville, Spain.
Tudor CiuleanuInstitutul Oncologic Cluj-Napoca, Cluj-Napoca, Romania.
Pilar Garcia-AlfonsoHospital General Universitario Gregorio Marañón, Madrid, Spain.
David C PortnoyWest Clinic, Memphis, TN, USA.
Eric Van CutsemUniversity Hospitals Gasthuisberg, Louvain, Belgium.
Kentaro YamazakiShizuoka Cancer Center, Shizuoka, Japan.
Philip R ClinganSouthern Medical Day Care Centre, Wollongong, Australia.
Jonathon PolikoffKaiser Permanente San Diego, San Diego, CA, USA.
Sara LonardiIstituto Oncologico Veneto IOV - IRCCS, Padua, Italy.
Lisa M O'BrienEli Lilly and Company, Indianapolis, IN, USA.
Ling GaoEli Lilly and Company, Bridgewater, NJ, USA.
Ling YangEli Lilly and Company, Bridgewater, NJ, USA.
David FerryEli Lilly and Company, Bridgewater, NJ, USA.
Federico NasroulahEli Lilly and Company, Buenos Aires, Argentina.
Josep TaberneroVall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo characterize ramucirumab exposure-response relationships for efficacy and safety in patients with metastatic colorectal cancer (mCRC) using data from the RAISE study.

methodsSparse pharmacokinetic samples were collected; a population pharmacokinetic analysis was conducted. Univariate and multivariate Cox proportional hazards models analyzed the relationship between predicted ramucirumab minimum trough concentration at steady state (C

resultsPharmacokinetic samples from 906 patients were included in exposure-efficacy analyses; samples from 905 patients were included in exposure-safety analyses. A significant association was identified between C

conclusionsExploratory exposure-response analyses suggested a positive relationship between efficacy and ramucirumab exposure with manageable toxicities in patients from the RAISE study with mCRC over the ranges of exposures achieved by a dose of 8 mg/kg every 2 weeks in combination with FOLFIRI.

Indexed as

AgedAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsColorectal NeoplasmsDisease-Free SurvivalFemaleHumansMaleRamucirumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsRamucirumabColorectal cancerExposure–responseFOLFIRIRamucirumabSecond line

Identifiers

PMID28744667
PMCPMC5573752

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Registered trials

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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.