Evidence map›Paper›PMID 41742069›Full record

ArticleBMC cancer2026

ERBITAG: Non-interventional study on the efficacy of cetuximab in first-line therapy in patients with RAS wild-type metastatic colorectal cancer.

Stephan W Sahm, Ulf Peter Neumann, Mark-Oliver Zahn, Michael Schwittay, Christoph Maintz, Thomas Goehler, Oleg Rubanov, Christiane Hering-Schubert, Jan Janssen, Karsten Stenzel and 2 more

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Stephan W SahmEthikrat (Vors.), Ketteler Krankenhaus, Lichtenplattenweg 85, Offenbach am Main, 63071, Germany. Stephan.Sahm@t-online.de.
Ulf Peter NeumannKlinik für Allgemein-, Viszeral- und Transplantationschirurgie, Universitätsklinikum Essen, Essen, Germany.
Mark-Oliver ZahnMVZ Onkologische Kooperation Harz, Goslar, Germany.
Michael SchwittayTumorzentrum und Hausarztpraxis Rötha, Rötha, Germany.
Christoph MaintzHämatologie-Onkologie, MVZ West GmbH Würselen, Würselen, Germany.
Thomas GoehlerHämatologie-Onkologie, Onkozentrum Dresden / Freiberg / Meißen, Dresden, Germany.
Oleg RubanovHämatologie-Onkologie, Praxis für Hämatologie und Onkologie, Hameln, Germany.
Christiane Hering-SchubertInnere Medizin III, St. Georgklinikum Eisenach, Eisenach, Germany.
Jan JanssenHämatologie-Onkologie, Hämatologie und internistische Onkologie Westerstede, Westerstede, Germany.
Karsten StenzelMedical Affairs Oncology, Merck Healthcare GmbH, Weiterstadt, Germany.
Julia ReinkeMedical Affairs Oncology, Merck Healthcare GmbH, Weiterstadt, Germany.
Friedrich OverkampOncoConsult Overkamp GmbH, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic colorectal cancer (mCRC) is a difficult-to-treat disease with poor clinical outcomes. Systemic chemotherapy in combination with targeted anti-EGFR therapy has expanded the treatment options for mCRC. However, the therapeutic efficacy of anti-EGFR regimens and relevant prognostic factors vary according to age, performance status and tumor location. The non-interventional ERBITAG study was performed to evaluate the efficacy and safety of cetuximab in first-line therapy in RAS WT mCRC patients under routine clinical practice.

methodsERBITAG is a non-interventional study of wild-type (WT) RAS mCRC patients initiating a first-line therapy with cetuximab from 2010 to 2018. Overall survival (OS) and progression-free survival (PFS) were analyzed using the Kaplan-Maier methods. χ²-test was used to compare selected categorial variables.

resultsOf a total of 728 patients included, baseline characteristics were: median 67 years, male sex 69%, ECOG performance status ≤ 1 81.3%, left-sided tumors 64.5%, liver metastasis 73.4% and prior hepatic metastasis resection before cetuximab-based treatment 16.4%. Median PFS was 10.9 months, median OS was 23.6 months and ORR was 58.0%. Resection rate of liver and/or lung metastases under cetuximab-based therapy was 13.9% and 18.9% of liver metastases. The most common treatment-emergent event (TEAE) was acne-like rash (all grades: 46.8%; grade 3–4: 4.7%). Subgroup analysis showed better outcomes in younger patients (ORR, OS), patients with left-sided tumors (ORR, PFS, OS) and lower grade tumors (ORR, PFS, OS), patients with resected liver and/or lung metastases (PFS, OS) and patients with treatment breaks (OS). Skin prophylaxis with systemic antibiotics and/or topical steroids (ORR, OS, PFS) was associated with better outcomes.

conclusionsThe ERBITAG study provides insights into the use of cetuximab in a large RAS WT mCRC cohort in real-life clinical practice in Germany. Cetuximab in combination with first-line chemotherapy demonstrates clinical outcomes and safety data similar to results from the other pivotal randomized controlled trials.

trial registrationStudy Number: EMR062202-515 ( https://www.pei.de/SharedDocs/awb/nis-0101-0200/0114.html ) Registered on 04-MAY-2010.

Indexed as

Antineoplastic Agents, ImmunologicalCetuximabColorectal NeoplasmsLiver NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedProgression-Free Survivalras ProteinsTreatment OutcomeAntineoplastic Agents, ImmunologicalCetuximabras ProteinsCetuximabCetuximab-based combinational chemotherapyColorectal cancerFirst-line therapyMetastatic colorectal cancerNon-interventional studyRAS WTSkin prophylaxis

Identifiers

PMID41742069
PMCPMC12951997

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.