A Phase-II Study Of TOMUDEX Plus Radiotherapy In Subject With Inoperable or Recurrent Rectal Cancer

• Confirmed diagnosis of inoperable/recurrent rectal cancer
• Age > 18 years
• At least 1 measurable lesion should be present
• WHO performance score \< 2
• Life expentancy of at least 12 weeks
• Subjects will be considered appropriate to receive systemic chemotherapy and pelvic radiotherapy
• Documented informed consent to participate in the trial

Exclusion Criteria:

• Previous systemic chemotherapy
• Previous radiotherapy to the planned exposure area
• Subjects with distant metastases
• (a)white blood cell \< 4.0x109/L (unless absolute neutrophil count is >2.0x109/L or (b) Platelet count \< 100x109/L
• Serum creatinine above the upper limit of the normal range
• (a) Serum bilirubin > 1.25 times the upper limit of the normal range or (b) Asparate aminotransferase(AST) or Alanine amiontransferase (ALT) >2.5 times the upper limit of the normal range
• Any severe concurrent medical condition which would make it undesirable, in the clinician's opinion, for the patient to participate in the trial or which would jeopardise compliance with the trial period
• Pregnancy or breast feeding. Women of childbearing age must use effective contraception
• Previous or current malignancies at other sites, with the exception of adequately treated in-situ carcinoma of the cervix uteri and basal or squamous cell carcinoma of the skin
• Patient participation in other studies