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VM-26 in colorectal carcinoma: A Southwest Oncology Group study

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Summary

In this multi-institutional phase II study, VM-26 or Teniposide was administered to forty-two patients with advanced colorectal cancer. Patients were initially treated at 60 mg/M2 daily for 5 days with dose adjustments depending on toxicity. One complete response and one partial response were observed lasting six and four months respectively. Leukopenia was severe in 40% of patients. No drug related deaths were seen. In this Southwest Oncology Group (SWOG) study, VM-26 appeared to have minimal benefit in advanced colorectal cancer.

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Address for offprints: Southwest Oncology Group (SWOG 8426), Operations Office, 5430 Fredericksburg Road, Suite #618, San Antonio, TX 78229, USA

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Oishi, N., Fleming, T.R., Laufman, L. et al. VM-26 in colorectal carcinoma: A Southwest Oncology Group study. Invest New Drugs 8, 93–95 (1990). https://doi.org/10.1007/BF00216931

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