Evidence map›Paper›PMID 30924091›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2019

Skeletal muscle loss during anti-EGFR combined chemotherapy regimens predicts poor prognosis in patients with RAS wild metastatic colorectal cancer.

O Köstek, N C Demircan, A Gökyer, A Küçükarda, B S Sunal, M B Hacıoğlu, H Eslame, S Solak, E Yılmaz, S Uzunoğlu and 3 more

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 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

13 authors at 1 institution in 1 country.

O KöstekDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey. osmankostek@hotmail.com.ORCID http://orcid.org/0000-0002-1901-5603
N C DemircanDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
A GökyerDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
A KüçükardaDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
B S SunalDepartment of Radiology, Trakya University School of Medicine, Edirne, Turkey.
M B HacıoğluDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
H EslameTrakya University School of Medicine, Edirne, Turkey.
S SolakDepartment of Radiology, Trakya University School of Medicine, Edirne, Turkey.
E YılmazDepartment of Radiology, Trakya University School of Medicine, Edirne, Turkey.
S UzunoğluDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
N TunçbilekDepartment of Radiology, Trakya University School of Medicine, Edirne, Turkey.
I ÇiçinDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
B ErdoğanDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Trakya University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe aimed to assess whether anti-EGFR combined chemotherapy regimens are related with loss of skeletal muscle mass and to compare cetuximab and panitumumab therapies in the aspect of skeletal muscle area change as well as to assess whether skeletal muscle mass loss has prognostic significance in the RAS wild mCRC patients. MATERIALS AND

methodsA total of 56 patients (30 patients in cetuximab arm and 26 patients in panitumumab) who had computed tomography images were retrospectively evaluated at the diagnosis and follow up during the treatment period before progression.

resultsDuring treatment period 24 patients (42.8%) had muscle loss. Of these, 7 (29.2%) patients were treated at first-line and 17 (70.8%) patients were treated at second-line setting. There was no significant difference in the aspect of skeletal muscle loss among cetuximab and panitumumab combined treatment regimens. Median PFS was 9.1 (8.6-9.6) months in muscle loss group and 13.9 (7.2-20.6) months in muscle stable group (p = 0.001). Median OS was 23.4 (95% CI 15.8-31.0) months in muscle stable group and 19.1 (95% CI 17.0-21.3) months in muscle loss group (p = 0.57) at first-line setting. For second-line, median OS was 21.2 (14.7-27.7) months in muscle stable group and 14.4 (6.0-22.4) months in muscle loss group (p = 0.003).

conclusionsDecrease in skeletal muscle mass before progression on CT imaging is an independent indicator for shorter PFS value in RAS WT mCRC patients who received anti-EGFR combined chemotherapy regimens at both the first and second-line settings. Beside that shorter overall survival values also were significantly seen in patients who had muscle loss during anti-EGFR therapy in the second-line setting.

Indexed as

AgedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCamptothecinCetuximabColorectal NeoplasmsErbB ReceptorsFemaleFluorouracilGenes, rasHumansLeucovorinMaleMiddle AgedMuscle, SkeletalMuscular AtrophyAntineoplastic Agents, ImmunologicalCamptothecinCetuximabEGFR protein, humanErbB ReceptorsFluorouracilLeucovorinOrganoplatinum CompoundsPanitumumabAnti-EGFR treatmentMetastatic colorectal cancerPrognosisSkeletal muscle mass

Identifiers

PMID30924091
OpenAlexW2926559506

What OpenQuestion holds

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Read underepoch 390

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.