Cm. Haskell et al., PHASE-II STUDY OF INTRAVENOUS ADENOSINE 5'-TRIPHOSPHATE IN PATIENTS WITH PREVIOUSLY UNTREATED STAGE IIIB AND STAGE-IV NONSMALL CELL LUNG-CANCER, Investigational new drugs, 16(1), 1998, pp. 81-85
Fifteen patients with Stage IIIB or IV non-small cell lung cancer gave
informed consent to receive three or more 96-hour infusions of ATP at
a dose of 50 mcg/kg/min or higher to determine whether ATP has antine
oplastic activity against this tumor type and to better define the spe
ctrum of toxicity for ATP given as a single agent. There were no objec
tive complete or partial responses observed. The median survival of th
e overall group was 187 days and the median time to tumor progression
was 113 days. The major toxic side effects were chest pain and dyspnea
, leading to the cessation of treatment in 5 patients. We conclude tha
t ATP at this dose and schedule of administration is an inactive agent
in patients with advanced non-small cell lung cancer.