Korean J Hematol 1991; 26(1):
Published online March 31, 1991
© The Korean Society of Hematology
안흥석, 이용철, 박창훈, 임창열
전북대학교 의과대학 내과학교실
16 adult patients with acute myelogenous leukemia received TAD induction
chromotherapy consisting of 7-day courses of 6-thioguanine (100mg/㎡, every 12 hours)
and ars-C (100mg/㎡, daily), and 3-day courses of daunorublcin (45mg/㎡, daily). The
patients who didn't achieve complete remission after the first course of TAD received
an additional course of a modified TAD consisting of 5-day courses of 6-thioguanine
and ara-C, and 2-day courses of daunorubicin. Drug doses were identical to those used
in the first course of TAD. Patients who achieved complete remission after the first or
the second course of TAD received an alternating maintenance chemotherapy with
ara-C/6-thioguanine and ara-C/daunorubicin(maximum eight courses). 12 patients(75%)
achieved complete remission. Median remission duration was 13 months and median
survival 13 months. Bone marrown was profoundly depreseed in most patients after
TAD. Other toxicities of TAD were anorexia, nausea, vomiting, headache, alopecia,
stomatitis, diarrhea, hepatotoxicity and skin discoloration. No substantial cardiac, renal or
neurological toxicity was observed. These results indicate that TAD regimen is effective
in the treatment of acute myelogenous leukemia.
Keywords Chemotherapy, Acute Myelogenous Leukemia
Korean J Hematol 1991; 26(1): 73-80
Published online March 31, 1991
Copyright © The Korean Society of Hematology.
안흥석, 이용철, 박창훈, 임창열
전북대학교 의과대학 내과학교실
Hong Seok Ahn, Yong Cheol Lee, Chang Hun Park, Chang Yeol Yim
Department of Internal Medicine, Chonbuk National University, Medical School, Chonju, Chonbuk, Korea
16 adult patients with acute myelogenous leukemia received TAD induction
chromotherapy consisting of 7-day courses of 6-thioguanine (100mg/㎡, every 12 hours)
and ars-C (100mg/㎡, daily), and 3-day courses of daunorublcin (45mg/㎡, daily). The
patients who didn't achieve complete remission after the first course of TAD received
an additional course of a modified TAD consisting of 5-day courses of 6-thioguanine
and ara-C, and 2-day courses of daunorubicin. Drug doses were identical to those used
in the first course of TAD. Patients who achieved complete remission after the first or
the second course of TAD received an alternating maintenance chemotherapy with
ara-C/6-thioguanine and ara-C/daunorubicin(maximum eight courses). 12 patients(75%)
achieved complete remission. Median remission duration was 13 months and median
survival 13 months. Bone marrown was profoundly depreseed in most patients after
TAD. Other toxicities of TAD were anorexia, nausea, vomiting, headache, alopecia,
stomatitis, diarrhea, hepatotoxicity and skin discoloration. No substantial cardiac, renal or
neurological toxicity was observed. These results indicate that TAD regimen is effective
in the treatment of acute myelogenous leukemia.
Keywords: Chemotherapy, Acute Myelogenous Leukemia
Ho Jung Choi, Juhee Shin, Sunghan Kang, Jin Kyung Suh, Hyery Kim, Kyung-Nam Koh, Ho Joon Im
Blood Res 2020; 55(4): 262-274Yoon Seok Choi
Blood Res 2020; 55(S1): S58-S62Il-Young Jang, Dok Hyun Yoon, Shin Kim, Kyoungmin Lee, Kwang-Kuk Kim, Young-Min Lim, Won-Ki Min, and Cheolwon Suh
Blood Res 2014; 49(1): 42-48