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. Author manuscript; available in PMC: 2010 Sep 2.
Published in final edited form as: Anticancer Drugs. 2010 Aug;21(7):716–723. doi: 10.1097/CAD.0b013e32833cb658

Table 7.

Summary of final response status assessments by patient

Primary diagnosis Assigned treatment Completed cycles of treatment Best overall overall responsea
Renal cell carcinoma Edotecarin + 5-FU/LV Cycle 3 PD
Pancreatic cancer Edotecarin + 5FU/LV Cycle 18 SD
Adenocarcinoma of pancreas Edotecarin + 5-FU/LV Cycle 3 PD
Epidermoid lung carcinoma Edotecarin + 5-FU/LV Cycle 3 PD
1/3 esophagus carcinoma Edotecarin + 5-FU/LV Cycle 9 SD
Adrenal carcinoma Edotecarin + 5-FU/LV Cycle 3 SD
Pancreatic adenocarcinoma Edotecarin + 5-FU/LV Cycle 3 PD
Hepatocarcinoma Edotecarin + 5-FU/LV Cycle 12 CR
Moderately differentiated adenocarcinoma duodenum Edotecarin + 5-FU (w/bolus) +LV Cycle 7 SD
Gastric carcinoid Edotecarin + 5-FU (w/bolus) +LV Cycle 9 SD
Ampullary cancer Edotecarin + 5-FU (w/bolus) +LV Cycle 6 SD
Small cell neuroendocrine carcinoma liver metastases Edotecarin + 5-FU (w/bolus) +LV Cycle 3 PD
Bronchus carcinoma Edotecarin + 5-FU (w/bolus) +LV Cycle 8 SD
Superior pole of left kidney cancer Edotecarin + 5-FU (w/bolus) +LV Cycle 3 PD

5-FU, 5-fluorouracil; CR, complete response; LV, leucovorin; PD, progression of disease; SD, stable disease.

a

As determined by the investigator.