Low-intensity induction chemotherapy before chemoradiotherapy for rectal cancer: 10-year overall survival in the LARC-RRP trial
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Updated: Jun 4, 2026

Robot-assisted Total Mesorectal Excision and Lateral Pelvic Lymph Node Dissection for Locally Advanced Middle-low Rectal Cancer
Published on: February 12, 2022
Anne Hansen Ree1,2, Sebastian Meltzer1, Kjersti Flatmark2,3,4
1Department of Oncology, Akershus University Hospital, 1478 Lørenskog, Norway.
Objectives:
Total neoadjuvant therapy (TNT) for locally advanced rectal cancer (LARC) often uses intensive oxaliplatin-based chemotherapy alongside standard radiotherapy to prevent metastatic progression. The optimal intensity of the chemotherapy component, given a contribution of radiotherapy to clonogenic cell elimination in the primary tumor, remains uncertain. We aimed to assess long-term outcomes of a TNT regimen with low-intensity induction chemotherapy before chemoradiotherapy, as evaluated in the LARC-RRP trial.
Methods:
Between 2005 and 2010, 87 LARC patients (36% with T4 organ-infiltrating tumor) were enrolled in the single-arm trial. Induction chemotherapy was given over 4 weeks prior to chemoradiotherapy and surgery. We report 10-year overall survival by tumor regression grade (TRG) and performed descriptive comparisons with contemporary trials whose experimental TNT arms used more intensive chemotherapy.
Results:
At 10 years, overall survival was 83% (95% confidence interval, 71-90) for patients with complete or near-complete tumor cell elimination in the surgical specimen (TRG 1-2; 70% of the cohort) versus 52% (95% confidence interval, 31-69) for others (log-rank P = .0005). LARC-RRP survival outcomes were comparable with those reported in more contemporary TNT trials.
Conclusions:
The LARC-RRP results raise the possibility that shorter-duration chemotherapy combined with standard radiotherapy may suffice to protect against systemic recurrence of high-risk LARC.
Advances In Knowledge:
These long-term data support investigation of less intensive chemotherapy within TNT regimens and may guide the design of risk-stratified TNT trials.