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Also, patients who discontinued treatment, or those who died from a treatment-related toxicity before response evaluation, were considered evaluable for response.
In addition, those patients who were developing rapid tumour progression, or those who died of progressive disease before the response evaluation, would also be considered evaluable for response.
All eligible patients were evaluated for survival and toxicity, and they were considered evaluable for response when they had completed three treatment cycles.
All of the eligible patients were evaluated for survival and toxicity, and all of the patients were considered evaluable for response.
Nine patients completed at least one 6 week cycle of treatment and were considered evaluable for response.
Thirty-two patients were therefore considered evaluable for response.
Similar(23)
All patients who received more than 6 vaccinations were considered evaluable for tumor response, and all patients entered were included in the survival analysis.
Patients who received two or more cycles of the protocol treatment were considered evaluable for tumour response and those who had completed one or more cycles were considered evaluable for toxicity.
Patients who completed at least 28 days of vaccination, corresponding to two vaccinations in Regimen I and four vaccinations in Regimens II and III, respectively, were considered evaluable for treatment response and survival (PP).
Analyses were performed on a modified intent-to-treat (mITT) population (patients were considered evaluable for tumor response if they had received at least one dose of ETPF combination).
Thirty-seven patients with tumour-related symptoms were considered evaluable for clinical benefit response.
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