Ettinger D S, Finkelstein D M, Donehower R C, Chang A Y, Green M, Blum R, Hahn R G, Ruckdeschel J C
Johns Hopkins Oncology Center, Baltimore, Maryland ff205.
Med Pediatr Oncol. 1989;17(3):197-201. doi: 10.1002/mpo.2950170306.
One hundred forty-four patients with non-small cell lung cancer, the majority (72%) of whom had received previous chemotherapy, were evaluable in this randomized phase II study of N-methylformamide (N-MF), spirogermanium, and 4-demethoxydaunorubicin. There were two partial responses, one each with spirogermanium and 4-demethoxydaunorubicin. There were eight life-threatening complications (mostly hematologic) and two lethal complications (N-MF, hematologic; 4-demethoxydaunorubicin, gastrointestinal). The overall survival ranged from 9 days to 533 days with a median of 17.6 weeks. The following factors were associated with poor survival: Poor initial performance status, prior weight loss, presence of liver or subcutaneous metastases.