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Vomiting associated with pentostatin and pentostatin plus alpha-interferon: unique pattern and potential mechanisms
Journal of Pain and Symptom Management
|August 1, 1990
Summary
Pentostatin, used for lymphoid cancers, frequently causes severe nausea and vomiting, especially when combined with alpha interferon. This side effect became the dose-limiting toxicity in many patients during clinical trials.
Area of Science:
- Oncology
- Pharmacology
Background:
- Pentostatin (2'-deoxycoformycin) is an antineoplastic agent for lymphoid malignancies.
- Existing data on pentostatin-induced nausea and vomiting (N&V) is insufficient for supportive care recommendations.
Purpose of the Study:
- To evaluate the incidence, duration, and severity of N&V in a phase I study of pentostatin.
- To identify N&V as a potential dose-limiting toxicity.
Main Methods:
- Phase I clinical trial assessing pentostatin, alone and with alpha interferon.
- Systematic recording of N&V incidence, onset, duration, and severity.
Main Results:
- Vomiting incidence increased from 20% (pentostatin alone) to 50% with concurrent alpha interferon.
- Nausea and vomiting was dose-limiting in 6 of 15 patients.
- Delayed onset (>24 hr) and prolonged duration (>48 hr) were common for vomiting episodes.
Conclusions:
- Nausea and vomiting is a significant and potentially dose-limiting toxicity of pentostatin, particularly with combination therapy.
- Delayed and prolonged N&V requires careful consideration for antiemetic management.
- Further research into mechanisms and optimal antiemetic strategies is warranted.