Background/Aim: Meckel's diverticulum carcinoma (MDCa) is extremely rare. It is often advanced when found, and the prognosis is poor. Effective treatment for this cancer has not yet been developed. We previously established a patient-derived xenograft (PDX) nude-mouse model of MDCa. In the present study, we investigated the efficacy of oxaliplatinum (L-OHP) and 5-fluorouracil (5-FU) on an MDCa PDX nude-mouse model. Materials and Methods: PDX mouse models of MDCa were divided into three groups (five mice per group): untreated control; L-OHP-treated; and 5-FUtreated. Tumor volumes of the three groups were compared after 2 weeks. Results: L-OHP arrested tumor growth (p=0.038) and 5-FU apparently eradicated the tumor (p=0.007). Conclusion: L-OHP and 5-FU are candidates for clinical first-line therapy of MDCa.Meckel's diverticulum (MD), a true diverticulum, is the most frequent congenital abnormality of the gastrointestinal tract, occurring in approximately 2% of the general population (1-9) with a reported incidence of cancer only 0.5% to 3.2%. MD carcinoma (MDCa) is extremely rare, as most tumors that arise in the MD are carcinoid (10). Because of its low incidence, there is as yet no established first-line chemotherapy, and prognosis is poor (10).In a previous study, a patient with MDCa, arising from gastric mucosa, failed first-line therapy with paclitaxel and cisplatinum and second-line therapy with S-1 and docetaxel. However, third-line chemotherapy with pemetrexed and carboplatinum resulted in reduction of the patient's ascites (11).Oxaliplatinum (L-OHP) is classified as a platinum-based cancer drug similar to cisplatinum (12). L-OHP inhibits DNA synthesis (13). In clinical practice, L-OHP is used primarily for advanced colorectal cancer (14).5-Fluorouracil (5-FU) is a fluoropyrimidine-antimetabolite chemotherapy agent (15), used for a variety of adenocarcinoma types, including gastric, liver, colorectal, and breast cancer (16,17).We have previously established a patient-derived xenograft (PDX) mouse model of MDCa by subcutaneously implanting MD carcinoma obtained from a patient into nude (nu/nu) mice ( 18). In the present study, we determined the efficiency of L-OHP and 5-FU using the PDX mouse model of MDCa.