# First-line anlotinib versus bevacizumab plus CapeOX in RAS/BRAF wild-type unresectable metastatic colorectal cancer (ANCHOR): a multicenter, prospective, randomized, phase 3 trial

Source: https://onco.cc/key-papers/paper-nct04854668-signal-transduct-target-ther-2026/  
OnCo record `paper-nct04854668-signal-transduct-target-ther-2026` (Key paper). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)"; commercial use needs a licence.

## TL;DR

Published report from the BRAF Wild Metastatic Colorectal Can trial registered as NCT04854668, in Signal transduction and targeted therapy (2026), chosen as the most cited paper whose own text cites the registry id.

## Summary

Bevacizumab plus chemotherapy is the standard first-line therapy for metastatic colorectal cancer (mCRC). To date, no phase 3 trial has compared first-line oral multitargeted TKI versus bevacizumab plus chemotherapy in RAS/BRAF wild-type mCRC. The open-label, noninferiority, randomized, phase 3 trial (ANCHOR; NCT04854668; CTR20210940) evaluated first-line anlotinib versus bevacizumab plus oxaliplatin and capecitabine (CapeOX) in this setting. Patients were centrally randomized (1:1) to receive 4-8 cycles of CapeOX in combination with either anlotinib (12 mg once daily on days 1-14) or bevacizumab (7.5 mg/kg on day 1) every 3 weeks, followed by maintenance therapy with anlotinib or bevacizumab plus capecitabine until unacceptable toxicity or disease progression. The primary endpoint was progression-free survival (PFS) assessed by an independent review committee in the intention-to-treat population. The hazard ratio (HR) for the noninferiority margin was 1.09. Between May 25, 2021, and August 30, 2023, 373 patients were assigned to the anlotinib group and 375 to the bevacizumab group. at February 2, 2025, the median follow-up was 25.1 months (95% confidence interval [CI] 23.8-26.3). The median PFS was 11.0 months (95% CI 9.8-11.2) in the anlotinib group versus 11.0 months (9.7-11.2) in the bevacizumab group (stratified HR, 1.00; 95% CI 0.84-1.18; p = 0.87). The incidences of grade ≥3 treatment-related adverse events were 64.9% and 44.8%, respectively. Compared with bevacizumab plus CapeOX, anlotinib plus CapeOX showed similar antitumor activity but failed to reach the prespecified noninferiority margin for PFS and was associated with increased manageable toxicity.

Indexed on Europe PMC as PubMed record 42675036 (DOI 10.1038/s41392-026-02938-4). Its abstract cites the registry id NCT04854668, which is how it was matched to this trial; no figure has been checked by an editor.

## Fields

- Kind: Key paper
- Last checked: 2026-09-22
- Tags: europepmc-ingest
- Journal: Signal transduction and targeted therapy
- Year: 2026
- DOI: 10.1038/s41392-026-02938-4
- Authors: Liu Y, Zhang Y, Lin R, et al.
- What it means: This is the paper Europe PMC returns for registry id NCT04854668 with the most citations, so it is the natural first reading for anyone following the BRAF Wild Metastatic Colorectal Can trial. Read the abstract above alongside the trial page and the registry entry; the record was linked automatically and its figures have not been checked by hand.
- Caveats: Matched to the trial by the registry id cited in the Europe PMC record; the summary reproduces the record's abstract and no figure has been verified against the full paper.

## Sources

- Signal Transduct Target Ther 2026: https://doi.org/10.1038/s41392-026-02938-4
- PubMed: https://pubmed.ncbi.nlm.nih.gov/42675036/
- Europe PMC: https://europepmc.org/article/MED/42675036
- ClinicalTrials.gov NCT04854668: https://clinicaltrials.gov/study/NCT04854668

## Connected records

- trials: [A Study of Anlotinib Hydrochloride Capsule Combined With Chemotherapy as First-line Treatment in Subjects With RAS/BRAF Wild Metastatic Colorectal Can](https://onco.cc/trials/nct04854668/)

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