Chinese Clinical Oncology

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Olanzapine combined granisetron and dexamethasone for the prevention of chemotherapyinduced emesis and nausea in cancer patients: A phase Ⅰ trial

YUAN Lingyan, JIAO Xiaodong, WANG Zhan, QIAN Jianxin, LI Li, WANG Jiejun   

  1. Department of Oncology, Shanghai Changzheng Hospital Affiliated to the Second Military Medical University, Shanghai 200072, China
  • Received:2013-01-11 Revised:2013-02-15 Online:2013-06-30 Published:2013-06-30
  • Contact: WANG Jiejun

Abstract: Objective To investigate the maximum tolerated dose of olanzapine for preventing emesis and nausea during chemotherapy in cancer patients. Methods This study was designed with olanzapine,using a six-cohort dose escalation of at least 3 patients per cohort,combining granisetron and dexamethasone for the prevention of chemotherapyinduced emesis and nausea in cancer patients. The initial dose cohort of olanzapine was 25mg; the terminal one was 20mg. Olanzapine was administered from one day before experiment to 14th day of experiment(d-1-d14) per night. If no dose-limiting toxicity was observed, the study could escalate to the next cohort. Results Eighteen patients were enrolled in the protocol and fifteen patients completed it. Two patient experienced a doselimiting toxicity(grade 3) of dry mouth and somnolence in 15mg cohort. Thus the study stopped on this cohort. In this study adverse events above grade 2 were somnolence, sedation, dizziness, akathisia, constipation, fatigue and bone marrow suppression.
Conclusion Olanzapine is well tolerated and safe in using recommended dose 15mg on d-1 to d14 per night.

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