Korean J Hematol 1996; 31(2):
Published online June 30, 1996
© The Korean Society of Hematology
현용준, 윤휘중, 이원욱, 김정희, 김시영, 조경삼
경희대학교 의과대학 내과학교실
Background: Adult lymphoblastic lymphoma was associated with a poor prognosis,
and long-term survivors were few. After the early-1980s, however, several investigators
have reported high therapeutic effects of ALL(acute lymphoblastic leukemia) protocols in
this disease. We evaluated clinical features of lymphoblastic lymphoma and the results
of L-l7M chemotherapeutic regimen, which was initially designed for therapy of ALL, in
adult patients with lymphoblastic lymphoma.
Methods: Fourteen Patients with lymphoblastic lymphoma received L-l7M
chemotherapy; 11 chemotherapy-naive patients, 3 previously chemotherapy-received
patients. L-l7M chromotherapy contained multiple drugs including vincristine,
prednisolone, adriamycin, cyclophosphamidle, daunorubicin, cytarabine, 6-thioguanine,
methotrexate, L-asparaginase, dactinomycin, and BCNU, which were employed in various
combinations during the induction, consolidation and maintenance phases.
Results: The age of patients ranged from 14 to 35 years, with a median of 23 years.
The male-to-female ratio was 1.3 : 1. The most common symptoms or signs were
multiple lymphnode enlargement. Five patients had mediastinal mass. Lymphoma
involved BM in 10 patients. Immunophenotyping study showed 9 T-cell type and 3
B-cell type. Three patients with B-cell type had shorter survival compared to T-cell
type. In 14 patients, median duration of survival after initial diagnosis was 229
weeks(7-379+). In evaluable patients(13), median duration of survival after
the star of L-l7M was 123 weeks(4-351+). Ten patients achieved complete
remission with L-l7M, and 8 of them are still in remission for duration of
18+to 345+weeks. Two out of ten patients(20%) relapsed in
lymph node and bone marrow. Median duration of granulocytopenia was 8 days(0∼34
days) during the induction phase and 17 days(6∼41 days) in consolidation phase.
Non-hematologic toxicities were nausea, vomiting, alopecia, stomititis, diarrhea, and
hepatotoxicity.
Conclusion: Our results suggest that L-l7M chemotherapy is effective in adult
lymphoblastic lymphoma.
Keywords Non-Hodgkin lymphoma, Adult Iymphoblastic Iymphoma, L-l7M chemorapy
Korean J Hematol 1996; 31(2): 289-298
Published online June 30, 1996
Copyright © The Korean Society of Hematology.
현용준, 윤휘중, 이원욱, 김정희, 김시영, 조경삼
경희대학교 의과대학 내과학교실
Yong Jun Hyun, Hwi Joong Yoon, Won Wook Lee, Jeong Hee Kim, Si Young Kim, Kyung Sam Cho
Department of Internal Medicine, College of Medicine, Kyung Hee University, Seoul, Korea
Background: Adult lymphoblastic lymphoma was associated with a poor prognosis,
and long-term survivors were few. After the early-1980s, however, several investigators
have reported high therapeutic effects of ALL(acute lymphoblastic leukemia) protocols in
this disease. We evaluated clinical features of lymphoblastic lymphoma and the results
of L-l7M chemotherapeutic regimen, which was initially designed for therapy of ALL, in
adult patients with lymphoblastic lymphoma.
Methods: Fourteen Patients with lymphoblastic lymphoma received L-l7M
chemotherapy; 11 chemotherapy-naive patients, 3 previously chemotherapy-received
patients. L-l7M chromotherapy contained multiple drugs including vincristine,
prednisolone, adriamycin, cyclophosphamidle, daunorubicin, cytarabine, 6-thioguanine,
methotrexate, L-asparaginase, dactinomycin, and BCNU, which were employed in various
combinations during the induction, consolidation and maintenance phases.
Results: The age of patients ranged from 14 to 35 years, with a median of 23 years.
The male-to-female ratio was 1.3 : 1. The most common symptoms or signs were
multiple lymphnode enlargement. Five patients had mediastinal mass. Lymphoma
involved BM in 10 patients. Immunophenotyping study showed 9 T-cell type and 3
B-cell type. Three patients with B-cell type had shorter survival compared to T-cell
type. In 14 patients, median duration of survival after initial diagnosis was 229
weeks(7-379+). In evaluable patients(13), median duration of survival after
the star of L-l7M was 123 weeks(4-351+). Ten patients achieved complete
remission with L-l7M, and 8 of them are still in remission for duration of
18+to 345+weeks. Two out of ten patients(20%) relapsed in
lymph node and bone marrow. Median duration of granulocytopenia was 8 days(0∼34
days) during the induction phase and 17 days(6∼41 days) in consolidation phase.
Non-hematologic toxicities were nausea, vomiting, alopecia, stomititis, diarrhea, and
hepatotoxicity.
Conclusion: Our results suggest that L-l7M chemotherapy is effective in adult
lymphoblastic lymphoma.
Keywords: Non-Hodgkin lymphoma, Adult Iymphoblastic Iymphoma, L-l7M chemorapy
Nisha Marwah, Manali Satiza, Niti Dalal, Sudhir Atri, Monika Gupta, Sunita Singh, Rajeev Sen
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