ArticleAmerican journal of cancer research2025
Combination of anti-epidermal growth factor receptor antibodies plus trifluridine-tipiracil as rechallenge strategy improves treatment outcomes in patients with RAS/BRAF wild-type refractory metastatic colorectal cancer.
Article in American journal of cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Advancements in Image-Based Analyses for Morphology and Staging of Colon Cancer: A Comprehensive Review.BioMed research international · 2025Pooled it
- Who Truly Benefits from Anti-EGFR Rechallenge in Metastatic Colorectal Cancer? From Clinical Enrichment to ctDNA-Guided Molecular Hyperselection.Journal of gastrointestinal cancer · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Trifluridine/tipiracil (FTD-TPI) plus bevacizumab is an established option for refractory metastatic colorectal cancer (mCRC). Rechallenging RAS/BRAF-wild-type tumours with an anti-EGFR antibody in combination with FTD-TPI is emerging, yet the two strategies have not been directly compared. We retrospectively identified consecutive RAS/BRAF-wild-type, chemotherapy-refractory mCRC patients treated at National Taiwan University Hospital between December 2018 and March 2023. All had received first-line anti-EGFR therapy; subsequent treatment comprised FTD-TPI with either anti-EGFR rechallenge (n = 20) or an anti-VEGF agent (n = 10). Anti-EGFR rechallenge yielded a higher objective response rate (30% vs 0%; P = 0.074) and disease-control rate (70% vs 30%; P = 0.440), plus numerically longer median progression-free (3.4 vs 2.3 months; P = 0.524) and overall survival (12.7 vs 9.9 months; P = 0.644). After adjustment for age, sex, tumour sidedness and time from metastatic diagnosis to FTD-TPI, anti-EGFR therapy remained the only independent predictor of response (posterior OR ≈ 7; 95% credible interval 1.1-66). These data suggest that FTD-TPI plus anti-EGFR rechallenge provides greater tumour shrinkage and at least comparable survival versus FTD-TPI plus anti-VEGF in heavily pre-treated, wild-type mCRC, supporting further prospective evaluation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.