Phase II trial of oral S-1 combined with gemcitabine in metastatic pancreatic cancer
2006

Combining S-1 and Gemcitabine for Pancreatic Cancer

Sample size: 33 publication 10 minutes Evidence: moderate

Author Information

Author(s): Nakamura K, Yamaguchi T, Ishihara T, Sudo K, Kato H, Saisho H

Primary Institution: Chiba University

Hypothesis

Can the combination of S-1 and gemcitabine improve treatment outcomes in metastatic pancreatic cancer patients?

Conclusion

The combination of gemcitabine and S-1 is well tolerated and shows a high response rate in patients with metastatic pancreatic cancer.

Supporting Evidence

  • 16 patients had objective responses, including one complete response and 15 partial responses.
  • The overall response rate was 48%.
  • Median survival time was 12.5 months.
  • 1-year survival rate was 54%.
  • Grade 3–4 toxicities included neutropenia (55%) and leucopenia (33%).

Takeaway

Doctors tested a new medicine called S-1 with another medicine called gemcitabine to help people with a serious type of cancer, and it worked pretty well.

Methodology

Patients received S-1 orally for 14 days and gemcitabine on specific days, with cycles repeated every 21 days.

Potential Biases

Potential selection bias due to the non-randomized nature of the trial.

Limitations

The study was limited to a small sample size and lacked a control group.

Participant Demographics

Median age was 61 years, with 64% male and 36% female participants.

Statistical Information

P-Value

p<0.05

Confidence Interval

95% CI, 33–65

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1038/sj.bjc.6603168

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