ArticleFrontiers in oncology2025
Oxaliplatin versus irinotecan as first-line therapy in metastatic colorectal cancer with prior adjuvant treatment: a retrospective study on efficacy, sequential therapy, and the impact of thrombocytopenia.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- 16S rRNA Gene Sequencing Analysis and Caspase-3 Expression by Propolis Ameliorated Oxaliplatin-Induced Toxicity in Female Rattus norvegicus Pre- and During Pregnancy.Biological trace element research · 2026Article
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Authors and funding
5 authors.
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Abstract
Background: The comparative efficacy of oxaliplatin versus irinotecan as first-line therapy in mCRC patients with prior adjuvant treatment remains unclear. Objectives: To compare the efficacy of first-line oxaliplatin-based versus irinotecan-based chemotherapy in metastatic colorectal cancer (mCRC) patients with prior adjuvant treatment and explore factors influencing survival outcomes. Methods: This retrospective single-center study analyzed 227 mCRC patients (2005-2014) receiving oxaliplatin (n=106) or irinotecan (n=121) as first-line therapy. Survival outcomes, treatment sequences, and adverse events were evaluated via multivariate analysis. Results: Compared with the irinotecan group, the oxaliplatin group had a numerically longer median OS (29.9 vs. 23.0 months; HR = 0.75, Conclusion: Despite the limitations of a retrospective, single-center design, first-line oxaliplatin provides superior OS in mCRC patients with prior adjuvant therapy, independent of the treatment sequence. The OS disparity stems from the differential use of chemotherapy interchange, driven by oxaliplatin-induced thrombocytopenia during adjuvant treatment, which may lead to premature regimen abandonment. Clinicians should prioritize thrombocytopenia prevention and avoid arbitrary oxaliplatin discontinuation. These findings highlight the importance of managing oxaliplatin-associated toxicity to preserve subsequent treatment options, though they require validation in prospective studies.
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