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Prediction of response to anti-EGFR antibody-based therapies by multigene sequencing in colorectal cancer patients.

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BMC Cancer2015PMID 26508446PMC4624582stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (7)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 7

Curated evidence

Evidence citing this paper (2)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
26508446
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–2 of 2 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
FBXW7 Mutation1
Cetuximab + PanitumumabSubstitutesMalignant Colorectal NeoplasmCURATED_BROADERPredictiveBSupports Resistance2accepted
EID718

65 patients were retrospectively analyzed for mutational profiles predictive of response to EGFR-inhibitors (cetuximab or panitumumab). FBXW7 mutation was found to be more prevalent in non-responders … (full text at CIViC)

PMID 26508446 · Lupini et al., 2015 · Open in CIViC

civic
SMAD4 Mutation1
Cetuximab + PanitumumabSubstitutesMalignant Colorectal NeoplasmCURATED_BROADERPredictiveBSupports Resistance2accepted
EID719

In a retrospective analysis of 65 patients with metastatic colorectal cancer, SMAD4 mutations were more common among patients with no benefit from EGFR-inhibition (cetuximab or panitumumab) (4 patient… (full text at CIViC)

PMID 26508446 · Lupini et al., 2015 · Open in CIViC

civic