Evidence map›Paper›PMID 31462288›Full record

Trial reportBMC cancer2019

No evidence for changes in skeletal muscle mass or weight during first-line chemotherapy for metastatic colorectal cancer.

Sami Antoun, Mohamed Amine Bayar, Valérie Dyevre, Emilie Lanoy, Cristina Smolenschi, Michel Ducreux

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

Trial report in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00423696 (Phase II Randomized Study of First-Line Therapy Comprising Bevacizumab and Irinotecan Hydrochloride, Leucovorin Calcium, and Fluorouracil), which is not on this map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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.

NCT00423696 phase2completednot on this map

Phase II Randomized Study of First-Line Therapy Comprising Bevacizumab and Irinotecan Hydrochloride, Leucovorin Calcium, and Fluorouracil (FOLFIRI) Versus Bevacizumab and Irinotecan Hydrochloride and Capecitabine (XELIRI) in Patients With Unresectable Metastatic Colorectal Cancer [ACCORD]

TypeinterventionalSponsorUNICANCERRan2006 to 2011Enrolled145ConditionsColorectal CancerArmsbevacizumab, capecitabine, fluorouracil, irinotecan hydrochloride, leucovorin calcium
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Chemotherapy-Induced Sarcopenia.Current treatment options in oncology · 2020
    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

6 authors at 1 institution in 1 country.

Sami AntounMedical Emergency Unit in Oncology, Gustave Roussy Cancer Campus, 94800, Villejuif, France. sami.antoun@gustaveroussy.fr.
Mohamed Amine BayarDepartment of Biostatics and Epidemiology, Gustave Roussy Cancer Campus, 94800, Villejuif, France.
Valérie DyevreDepartment of Biostatics and Epidemiology, Gustave Roussy Cancer Campus, 94800, Villejuif, France.
Emilie LanoyDepartment of Biostatics and Epidemiology, Gustave Roussy Cancer Campus, 94800, Villejuif, France.
Cristina SmolenschiDepartment Medical Oncology, Gustave Roussy Cancer Campu, 94800, Villejuif, France.
Michel DucreuxDepartment Medical Oncology, Gustave Roussy Cancer Campu, 94800, Villejuif, France.
Institut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies over the past 10 years strongly support an association between skeletal muscle mass (SMM) depletion and outcome in metastatic colorectal cancer (mCRC). Factors influencing SMM changes over time are, however, poorly studied. We analyzed the impact of SMM on overall survival and chemotherapy toxicities in mCRC patients treated with first-line chemotherapy. Changes in weight and body composition were evaluated during follow-up.

methodsPatients enrolled in the randomized phase II ACCORD trial comparing two chemotherapy regimens were screened. Body composition parameters (SMM, adipose tissue) were assessed prospectively with computed tomography (CT) imaging, and toxicities were recorded. Mixed models were used to assess weight and BC changes during 4 months of treatment follow-up.

resultsAmong 145 patients included in ACCORD, 76 had available baseline CT scans and were included in the current study. Mean age was 60.6 ± 10.0 years, 50% were women, 82% had colon cancer, and 62% had two or more metastatic sites. At baseline, 49% had lost at least 5% of their initial weight, including 26% who had lost more than 10%; 53% had SMM depletion. In this homogenous cohort, there were no statistically significant associations between SMM depletion and overall survival, progression-free survival or chemotherapy toxicity. There were no decreases in weight or SMM during follow-up. Weight and SMM changes were not influenced by diarrhea either grade 3-4 or any grade (reported in 74% of patients). For patients with weight loss ≥10% at baseline, SMM increased significantly after 4 months of follow-up and after disease stabilization following chemotherapy (P = 0.008).

conclusionsIn a homogenous mCRC cohort, SMM depletion was not associated with survival or chemotherapy toxicity. Despite most patient experiencing diarrhea, no changes in weight or SMM were found during 4 months of follow-up. However, hypotheses deriving from our exploratory study have to be tested in further larger sample size studies.

trial registrationClinicaltrials.gov NCT00423696 (2011).

Indexed as

AgedAntineoplastic AgentsBody CompositionBody WeightColorectal NeoplasmsFemaleHumansMaleMiddle AgedMuscle, SkeletalNeoplasm MetastasisProspective StudiesSurvival AnalysisTomography, X-Ray ComputedTreatment OutcomeAntineoplastic AgentsBody compositionChemotherapy toxicityMetastatic colorectal cancerMuscle mass depletionOverall survivalWeight loss

Identifiers

PMID31462288
PMCPMC6714393
OpenAlexW2970328232

What OpenQuestion holds

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LicenceCC BY
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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.