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      Adjuvant Chemotherapy with Etoposide, 5-Fluorouracil and Leucovorin(ELF) in Gastric Cancer

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      https://www.riss.kr/link?id=A76517442

      • 저자

        Han Jo Kim (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Yong Kwan Lee (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Yun Seok Jung (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Hyun Jung Kim (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Sang Cheol Lee (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Sang Byung Bae (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Chan Kyu Kim (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Nam Su Lee (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Kyu Taeg Lee (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Sung Kyu Park (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Jong Ho Won (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Dae Sik Hong (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea) ;  Hee Sook Park (Department of Hematology-Oncology, department of internal medicine Soonchunhyang University College of Medicine, Seoul, Korea)

      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2008

      • 작성언어

        Korean

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      • 자료형태

        학술저널

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        123-134(12쪽)

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      다국어 초록 (Multilingual Abstract)

      Background: Gastric cancer is one of a major health problem and leading cause of cancer mortality despite worldwide decline in incidence. Surgical resection is the only treatment modality of proven effectiveness. Many phase III trials of adjuvant ther...

      Background: Gastric cancer is one of a major health problem and leading cause of cancer mortality despite worldwide decline in incidence. Surgical resection is the only treatment modality of proven effectiveness. Many phase III trials of adjuvant therapy have been conducted, however postoperative treatment modalities have not proven to be superior to postsurgical observation alone. We evaluated the effect of etoposide, leucovorin, 5-fluorouracil(ELF) regimen on the prevention of relapse and survival benefit after postoperative adjuvant chemotherapy.
      Material and Methods: Our study is retrospective, non-randomized study without controlled group. Between March 1998 and January 2005, 41 patients with completely resected gastric cancer received six courses of ELF chemotherapy of 4 weeks cycle. Endpoints were toxicities of treatment, overall survival, disease free survival.
      Results: Fourty one patients were entered into the trial. According to American Joint Comittee for Cancer screening(AJCC) TNM stage, 5 cases were in stage IB, 14 II, 13 IIIA, 5 IIIB, respectively and 4 cases were in stage IV without distant metastasis. With a median follow-up time of 40.3 months, 4-years overall survival and disease free survival was 68%, 63.7%, respectively. Severe neutropenia was observed in 19.5%, anemia was 2.4%, and thrombocytopenia was 2.4%. Severe nausea and vomiting was observed in 7.3%, but diarrhea, mucositis, alopecia, convulsion, edema and therapy related death was not observed.
      Conclusions : The ELF adjuvant chemotherapy may be effective for resectable gastric cancer with minimal toxicities, but randomized multicenter controlled phase III study is needed to confirm its efficacy and safety.

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