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Holch, Julian Walter ORCID logoORCID: https://orcid.org/0000-0002-4755-0179; Ohnmacht, Alexander J.; Stintzing, Sebastian ORCID logoORCID: https://orcid.org/0000-0002-3297-5801; Heinrich, Kathrin ORCID logoORCID: https://orcid.org/0000-0003-3580-2313; Weiss, Lena ORCID logoORCID: https://orcid.org/0000-0002-8101-3529; Probst, Victoria ORCID logoORCID: https://orcid.org/0009-0008-8038-7351; Stahler, Arndt ORCID logoORCID: https://orcid.org/0000-0003-1041-0137; Fischer von Weikersthal, Ludwig; Decker, Thomas; Kiani, Alexander ORCID logoORCID: https://orcid.org/0000-0002-2494-4087; Kaiser, Florian; Heintges, Tobias; Kahl, Christoph; Kullmann, Frank ORCID logoORCID: https://orcid.org/0000-0001-5575-1010; Link, Hartmut ORCID logoORCID: https://orcid.org/0000-0002-9659-0265; Höffkes, Heinz-Gert; Moehler, Markus; Modest, Dominik Paul; Menden, Michael P. und Heinemann, Volker ORCID logoORCID: https://orcid.org/0000-0002-1349-3321 (2. Mai 2025): FOLFIRI with cetuximab or bevacizumab in RAS wild-type metastatic colorectal cancer: Refining first-line treatment selection by combining clinical parameters. In: European Journal of Cancer, Bd. 220, 115388 [PDF, 1MB]

Abstract

Background

Primary tumor sidedness (PTS) with discrimination of left-sided (LC) and right-sided tumors (RC) guides patient selection for targeted first-line therapy in RAS wild-type (RAS-WT) metastatic colorectal cancer (mCRC). This study assessed the hypothesis whether considering PTS with additional clinical parameters better predicts the treatment benefit of targeted first-line treatment.

Methods

In FIRE-3, first-line treatment with folinic acid, fluorouracil and irinotecan (FOLFIRI) plus cetuximab (FOLFIRI/Cet) was compared to FOLFIRI plus bevacizumab (FOLFIRI/Bev) in patients with RAS-WT mCRC and unresectable metastasis. We evaluated whether combining PTS with number of metastatic sites (NOM), liver-limited disease status (LLD), age, sex, or carcinoembryonic antigen level (CEA) better predicts treatment benefit regarding overall survival (OS). Here, Cox regression models with second-order interactions were applied. Further, the results were validated by policy learning and Lasso regression analysis.

Findings

Among 400 RAS-WT mCRC patients, combining PTS with LLD status in a Cox regression model outperformed PTS alone for predicted treatment benefit (P = 0·005; c‑index=0·603). Significant OS benefit from FOLFIRI/Cet over FOLFIRI/Bev was observed in LC/non-LLD patients (HR=0·62; 95 %-confidence interval [CI]=0·46–0·82; P = 0·002), but mitigated in LC/LLD patients (HR=0·83; 95 %-CI=0·53–1·29; P = 0·400). In RC/non-LLD patients, FOLFIRI/Bev demonstrated a significant OS advantage over FOLFIRI/Cet (HR=2·09; 95 %‑CI=1·20–3·63; P = 0·010). However, RC/LLD patients showed potential benefit from FOLFIRI/Cet, though not statistically significant (HR=0·59; 95 %-CI=0·25–1·39; P = 0·218).

Interpretation

Incorporating PTS and LLD status might improve selection of targeted first-line treatment in RAS-WT mCRC patients. FOLFIRI/Cet appears to be particularly beneficial for LC/non-LLD patients with mitigated benefit in patients with LC/LLD. In contrast, FOLFIRI/Bev is significantly favoured over FOLFIRI/Cet in patients with RC/non-LLD. Notably, RC/LLD patients may still benefit from anti-EGFR therapy despite right-sided primary tumor. These results are hypothesis-generating and warrant further validation.

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