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Colon Cancer · Medical Oncology

MOSAIC

In resected stage II/III colon cancer, does adding oxaliplatin to fluoropyrimidine improve disease control and survival?

Population
2246 patients with completely resected stage II or III colon cancer
5-year DFS
73.3% vs 67.4%
Absolute improvement 5.9 points; NNT 17
6-year OS
78.5% vs 76.0%
Stage III: 72.9% vs 68.7%
Grade 3 sensory neuropathy
12.5% vs 0.2%
Absolute increase 12.3 points; NNH 8

Absolute Effect

NNT: 17, based on 5-year disease-free survival. The absolute DFS gain was 5.9 percentage points.

NNH: 8, based on grade 3 sensory neuropathy. Oxaliplatin introduced a substantial cumulative neurologic toxicity burden that became central to later duration-de-escalation studies.

Clinical interpretation

MOSAIC established oxaliplatin-containing adjuvant therapy as an important efficacy advance, but its absolute benefit must be weighed against neuropathy. This benefit–harm tension is precisely why treatment duration and patient risk matter.

Primary source

André T, et al. J Clin Oncol. 2009;27:3109–3116.

Read the primary publication →

Current-practice context · reviewed 14 October 2026

MOSAIC established the benefit of adding oxaliplatin to adjuvant fluoropyrimidine chemotherapy for stage III colon cancer, with a more selective role in high-risk stage II disease. Current decisions balance recurrence risk, mismatch-repair status, comorbidity, neuropathy risk and duration data from IDEA; do not treat every stage II patient with oxaliplatin-based chemotherapy.

MOSAIC primary report ↗ · Current guideline guidance ↗