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All 45 patients were evaluable for tolerability.
Patients were evaluable for tolerability and efficacy if they had received at least one and four courses of treatment, respectively.
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All patients were evaluable for safety analysis and efficacy evaluation.
All patients were evaluable for safety.
14 patients were evaluable for pharmacokinetic analysis.
All patients were evaluable for toxicity and 31 (78%) were evaluable for response.
infusion every 4 weeks) and were evaluable for toxicity and 18 (15 NSCLC, 3 SCLC) were evaluable for efficacy.
A total of 28 patients were evaluable for tumour response (Figure 2).
Seventy-nine patients were evaluable for safety, and data from 70 patients were used for efficacy analysis.
Results: Ten patients were enrolled, and 9 were evaluable for response.
Results: all patients were evaluable for response and toxicity (intention to treat analysis).
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