Experiment 1142694

Details

PropertyValue
Pharmacology
Administration routeIV
OrganismEmpty organism
CitationISSEL,BF: ELNHORN,LH: COMIS,RL: LAWSON,RD: BAKER,LH: HARVEY,HA: LANOTTI,VA: WAMPLER,GL: DANIELS,JR: ANDERSON,PN: HONG,WK: RENTSCHLER,RE: PIKLER,GM: MAROUN,JA: WERNZ,JC: ROSENBAUM,PF:. (1985). MULTICENTER PHASE II TRIAL OF ETOPOSIDE IN REFRACTORY SMALL CELL LUNG CANCER.. 69(1)
Amount utilized
Compound isolated
DiseaseIN THIS MULTICENTER PHASE II TRIAL ON ONE HUNDRED AND SIXTEEN PATIENTS WITH REFRACTORY SMALL CELL LUNG CANCER. PATIENTS WERE TREATED INITIALLY ON DAYS 1-5 IV WITH COURSES REPEATING EVERY 3-4 WEEKS WITH 80MG/SQ.M. SUBSEGUENT COURSES WERE DE-ESCALATED BY 20% TO MAINTAIN BLOOD COUNT. THIRTY ONE PATIENTS RECEIVE THE DRUG BY IV THE FIRST DAY AND THEN ORALLY DAYS 2-5 AT 160MG/SQ.M. THERE WAS ONE COMPLETE REMISSION AND 10 PARTIAL REMISSIONS ON THE REGULAR IV SCHEDULE. ON THE IV-PO SCHEDULE, 4 PATIENTS ACHIEVED PARTIAL REMISSION. LEUKOPENIA WAS SEEN IN ALL PATIENTS AND THROMBOCYTOPENIA WAS SEEN IN 25%. FIVE PATIENTS IN THE IV GROUP AND 1 PATIENT IN THE IV-PO GROUP DIED OF GRANULOCYTOPENIA RELATED SEPSIS. NON-HEMATOLOGICAL TOXICITY INCLUDED NAUSEA AND VOMITING WHICH OCCURRED IN 23% OF THE PATIENTS AND ANOREXIA WHICH OCCURRED IN 10%.
Dose amount80.0 MG
Number1
Qualitative resultEQUIVOCAL
AnimalHUMAN ADULT
Per unitSQ M BODY SURFACE
Dose expressionDOSE