Impact of anti-EGFR and anti-VEGF antibodies on survival in BRAF <sup>V600E</sup> mutated metastatic colorectal cancer: A pooled analysis of eight clinical trials performed in the first-line treatment of mCRC (German AIO Study Group).

L Lena Weiss S Sebastian Stintzing D Dominik Paul Modest L Ludwig von Weikersthal (MVZ Praxis für Hämatologie und Internistische Onkologie, Amberg, Germany) A Arndt Stahler (Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Berlin, Germany) A Anke C. Reinacher-Schick (COLOPREDICT Platform and Department of Hematology, Oncology and Palliative Care, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany) T Thomas Decker (16Oncological Practice, Ravensburg, Germany) V Victoria Probst K Kathrin Heinrich I Ingo Schwaner (10Onkologische Schwerpunktpraxis Kurfürstendamm, Berlin, Germany) F Florian Kaiser (8ÜBAG-MVZ Dr. Vehling-Kaiser GmbH, Landshut, Germany) R Rudolf Pihusch (MVZ Praxis Pihusch, Rosenheim, Germany) M Martin Fuchs (Staedt. Klinikum Muenchen GmbH, Munich, Germany) S Swantje Held (AIO-Studien-gGmbH, Berlin, Germany) A Annabel Helga Sophie Alig (Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Berlin, Germany) B Birgit Gruenberger (Universitätsklinikum Wiener Neustadt, Wiener Neustadt, Austria) G Gerald W. Prager (Department of Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria) D David Tougeron (Department of Hepatology and Gastroenterology, Poitiers University Hospital, Poitiers, France) J Julien Taieb V Volker Heinemann

Abstract

3543 Background: BRAF V600E mutation in metastatic colorectal cancer (mCRC) is associated with poor prognosis. Registrational approval of anti-EGFR antibodies does not exclude their use in BRAF V600E mutated (mut) mCRC, while current guidelines explicitly advise against the use of anti-EGFR-directed therapy and recommend the use of chemotherapy plus anti-VEGF antibodies. The present analysis of single-patient data evaluates the therapeutic benefit from anti-EGFR- vs. anti-VEGF-directed therapy in BRAF V600E mut mCRC. Methods: We conducted a pooled analysis of eight first-line AIO-studies (FIRE-1, FIRE-3, FIRE-4, FIRE-4.5, CIOX, XELAVIRI, PANAMA, VOLFI) including 251 evaluable pts with BRAF V600E mut and RAS wild-type mCRC. Right-sided primary tumors (RSPT) included tumors from the caecum to the colon transversum, while left-sided tumors (LSPT) included the splenic flexure to the rectum. Results: Of 251 BRAF V600E mut pts, exact primary tumor location was available in 230 pts. In this cohort, 117 were male (50.9%) and 113 female (49.1%). LSPT was observed in 106 (46.1%) pts compared to 124 (53.9%) with RSPT. In the entire cohort, median OS (mOS) of LSPT vs. RSPT did not differ significantly (15.2 months vs. 13.4 months; HR 0.96; 95% CI, 0.70–1.29; P=0.77). Pts with LSPT showed a numerical survival benefit with anti-EGFR therapy compared to anti-VEGF therapy (17.8 months vs. 11.8 months; HR 0.71; 95% CI, 0.45–1.14; P=0.16). This effect was observed independent of sex. In contrast, pts with RSPT showed a trend towards inferior outcome with anti-EGFR vs. anti-VEGF therapy (11.6 months vs. 17.1 months; HR 1.31; 95% CI, 0.84–2.05; P=0.23). This effect was primarily driven by females, who experienced a significant survival disadvantage with anti-EGFR therapy (10.2 months vs. 17.1 months; HR 1.85; 95% CI, 1.05–3.25; P=0.031). For males, however, both anti-VEGF and anti-EGFR antibodies were associated with comparable outcome. Conclusions: The present analysis performed in the first-line treatment of BRAF V600E mut mCRC suggests a survival benefit from anti-EGFR antibodies in pts with LSPT, independent of gender. Male pts with RSPT appear to derive comparable benefit from anti-EGFR and anti-VEGF antibodies, while female pts exhibit a survival disadvantage from anti-EGFR antibodies. Clinical trial information: NCT00433927 (FIRE-3), NCT02934529 (FIRE-4), NCT04034459 (FIRE-4.5), NCT01249638 (ML22011), NCT00254137 (CIOX), NCT01991873 (PANAMA), NCT01328171 (VOLFI). [clinicaltrials.gov].

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 3543-3543
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

L

Lena Weiss

S

Sebastian Stintzing

D

Dominik Paul Modest

L

Ludwig von Weikersthal

MVZ Praxis für Hämatologie und Internistische Onkologie, Amberg, Germany

A

Arndt Stahler

Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Berlin, Germany

A

Anke C. Reinacher-Schick

COLOPREDICT Platform and Department of Hematology, Oncology and Palliative Care, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany

T

Thomas Decker

16Oncological Practice, Ravensburg, Germany

V

Victoria Probst

K

Kathrin Heinrich

I

Ingo Schwaner

10Onkologische Schwerpunktpraxis Kurfürstendamm, Berlin, Germany

F

Florian Kaiser

8ÜBAG-MVZ Dr. Vehling-Kaiser GmbH, Landshut, Germany

R

Rudolf Pihusch

MVZ Praxis Pihusch, Rosenheim, Germany

M

Martin Fuchs

Staedt. Klinikum Muenchen GmbH, Munich, Germany

S

Swantje Held

AIO-Studien-gGmbH, Berlin, Germany

A

Annabel Helga Sophie Alig

Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Berlin, Germany

B

Birgit Gruenberger

Universitätsklinikum Wiener Neustadt, Wiener Neustadt, Austria

G

Gerald W. Prager

Department of Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria

D

David Tougeron

Department of Hepatology and Gastroenterology, Poitiers University Hospital, Poitiers, France

J

Julien Taieb

V

Volker Heinemann