Irinotecan, cisplatin and mitomycin in inoperable gastro-oesophageal and pancreatic cancers – a new active regimen
2002

New Treatment for Inoperable Gastro-Oesophageal and Pancreatic Cancers

Sample size: 45 publication 10 minutes Evidence: moderate

Author Information

Author(s): Slater S, Shamash J, Wilson P, Gallagher C J, Slevin M L

Primary Institution: St Bartholomew's Hospital

Hypothesis

Can a combination of irinotecan, cisplatin, and mitomycin improve treatment outcomes for inoperable gastro-oesophageal and pancreatic cancers?

Conclusion

The combination of irinotecan, mitomycin, and cisplatin shows promise in treating inoperable gastro-oesophageal and pancreatic cancers, with a response rate of 42% and median survival times of 9.5 months and 8 months, respectively.

Supporting Evidence

  • 42% of patients with gastro-oesophageal cancer showed a response to the treatment.
  • Median survival for gastro-oesophageal cancer patients was 9.5 months.
  • 42% of patients with pancreatic cancer also responded to the treatment.
  • Median survival for pancreatic cancer patients was 8 months.
  • Five treatment-related deaths occurred during the study.

Takeaway

Doctors tested a new mix of three cancer drugs on patients who couldn't have surgery, and it helped many of them live longer.

Methodology

Patients with inoperable cancer were treated with a combination of irinotecan, cisplatin, and mitomycin, and their responses were evaluated after six cycles of treatment.

Potential Biases

The study may have bias due to the limited number of patients and the high drop-off rate from treatment.

Limitations

The study had a small sample size and a high rate of non-evaluable patients due to toxicity.

Participant Demographics

Patients included 31 with gastro-oesophageal cancer and 14 with pancreatic cancer, with varying performance statuses.

Statistical Information

P-Value

0.0018

Confidence Interval

95% c.i. 6.7, 15.2 for gastro-oesophageal cancer; 95% c.i. 2.9, 24.7 for pancreatic cancer

Statistical Significance

p=0.0018

Digital Object Identifier (DOI)

10.1038/sj.bjc.6600553

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