The purpose of this study is to help answer the following research questions: If the study drug Pemetrexed can help patients with rectal cancer; If molecular biological parameters are correlated respectively changing due to cytotoxic treatment with Pemetrexed; To evaluate adverse events
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
37
500 mg/m2, intravenous (IV), every 21 days x 3 cycles
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Gothenburg, Sweden
Feasibility of Pemetrexed Prior to Surgery
Feasibility was defined as the ability to receive the total planned dose of Pemetrexed administered over a period of no more than 9 weeks permitting scheduling conflict. A ±5 percent variance in the calculated total dose was allowed.
Time frame: 3 cycles (21-day cycles)
Pathological Complete Response (pCR)
Pathological complete response was defined as the absence of any tumor cells.
Time frame: surgery following 3 cycles (21-day cycles) of chemotherapy
Number of Participants With Complete Tumor Resection
Time frame: surgery following 3 cycles (21-day cycles) of chemotherapy
Number of Participants Receiving Sphincter Saving Surgery
Time frame: surgery following 3 cycles (21-day cycles) of chemotherapy
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