Colorectal cancer research emphasizes screening, immunotherapy for MSI-high tumors, and targeted therapies for specific mutations.
In the randomized, open-label COMMIT trial (NRG-GI004/SWOG-S1610), 82 patients with previously untreated dMMR/MSI-H metastatic colorectal cancer were randomized 1:1 to mFOLFOX6/bevacizumab/atezolizumab (FFX/bev/atezo) or atezolizumab alone. At the November 6, 2025 cutoff (median follow-up 46 months), progression-free survival favored the combination: HR=0.42 (95% CI, 0.22–0.80; P=0.0068), with median PFS of 24.5 versus 5.3 months.
Part 1 of a phase 1 trial of RO7589831 (VVD-133214), a covalent Werner syndrome helicase inhibitor, enrolled 88 patients with MSI and/or dMMR advanced solid tumors who had progressed on standard therapies. Among 66 MSI efficacy-evaluable patients, the disease control rate (DCR) was 74.2% (95% CI 63.9–82.9; 49/66) and the objective response rate (ORR) was 10.6% (7/66, confirmed RECIST v.1.1 partial responses).
A multicohort analysis of 589,766 adults aged 40 to 74 years without prior cancer, drawn from the Shanghai Men’s Health Study, the Shanghai Women’s Health Study and UK Biobank, estimated how much of the higher cancer incidence in males is attributable to 11 lifestyle factors and health conditions.
PATHFINDER 2, a prospective, interventional cohort study of 35,878 adults aged 50 and older with no clinical suspicion of cancer, evaluated the performance and safety of a blood-based multi-cancer early detection (MCED) test that analyzes cell-free DNA methylation patterns to detect a shared cancer signal and predict its tissue of origin.
An open-label phase 1b expansion cohort within a larger basket study tested Fc-enhanced anti-CTLA-4 antibody botensilimab plus anti-PD-1 antibody balstilimab in 123 patients with microsatellite-stable metastatic colorectal cancer without active liver metastases, most of whom were heavily pretreated.
A single-center, non-randomized phase 2 basket trial tested ado-trastuzumab emtansine (T-DM1) across five disease-specific cohorts of HER2-amplified solid tumors, asking whether a shared molecular driver predicts benefit from a HER2-targeted antibody-drug conjugate regardless of tumor origin.
A registry-based analysis of 11,681 US interventional cancer trials registered on ClinicalTrials.gov between 2008 and 2024 found that industry sponsors now outnumber federal sponsors nearly 5 to 1 (4.53-to-1 overall), with the ratio widening from 2.72-to-1 in 2008–2012 to 6.44-to-1 in 2019–2024.
The phase III STELLAR trial (NCT02533271) randomly assigned 591 patients with distal or middle-third locally advanced rectal cancer to a short-course radiotherapy-based total neoadjuvant therapy regimen (SCRT-TNT) or standard long-course chemoradiotherapy (CRT); this update reports 5-year outcomes at a median follow-up of 68.7 months.
Retrospective, single-center biomarker cohort study of 39 patients with dMMR metastatic colorectal cancer treated with anti-PD-1 monotherapy at Mayo Clinic, using integrated exome, transcriptome, and immune-repertoire profiling to test whether quantitative MSI burden — not just binary MSI-high status — predicts benefit from checkpoint blockade
Open-label, single-center phase I dose-escalation and dose-expansion trial of IM96, an autologous GUCY2C-targeted CAR T-cell product, in 20 treated patients with microsatellite-stable, third- or later-line metastatic colorectal cancer — a population with very few remaining options
Retrospective subset analysis of the CIRCULATE-Japan GALAXY registry (298 patients with resected colorectal liver metastases) testing whether ctDNA-defined molecular residual disease (MRD) status can identify who actually benefits from adjuvant chemotherapy (ACT) after liver resection