Korean J Hematol 1996; 31(1):

Published online March 31, 1996

© The Korean Society of Hematology

불응성 다발성 골수종 환자에 대한 VAD(Vincristine, Doxorubicin, Dexamethasone) 복합화학요법의 제 2상 임상연구

이종태, 김인호, 안진석, 이기형, 김태유, 박영이, 김효수, 허대석, 방영주

서울대학교 의과대학 내과학교실

Phase Ⅱ Trial of VAD (Vincristine, doxorubicin, and Dexamethasone) in Refractory Multiple Myeloma

Jong Tae Lee, In Ho Kim, Jin Seok Ahn, Ki Hyeong Lee, Tae Yu Kim, Young I Park, Hyo Soo Kim, Dae Seog Heo, Yung, Jue Bang, Seonyang Park, Byoung Kook Kim, Noe Kyeong Kim

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea

Abstract

Background : Multiple myeloma(MM) remains as an incurable malignant disorder as a
result of resistance to chemotherapy. With standard dose of alkylating agents such as
melphalan and prednisone (MP) or alkylating agent combinations with or without
doxorubicin, responses are achieved in approximately 50% of patients, and relapse
typically ensues after a median of 18 months. Therefore, salvage therapy becomes
important for half of the patients with newly diagnosed MM who fail to achieve
remission(primary refractory) and for responders who have a relapse despite
myelosuppressive doses of chemotherapy(secondary refractory). The VAD regimen,
comprising vincristine and doxorubicin given by continuous infusion along with high
doses of dexamethasone has achieved a marked tumor reduction in about one half of
patients. So we investigated the efficacy of VAD regimen for patients with refractory
multiple myeloma.
Methods: Twenty-two patients with refractory multiple myeloma were treated
according to the VAD protocols proposed by Barlogie et al.
Results: Of the 21 evaluable patients who completed at least one course of therapy, 9
had a complete response(43%). The response rates were 23% for primary refractory
disease patients and 75% for those with secondary refractory disease(P<0.05). The
median duration of response was 3 months(2∼18months) and the median survival for all
22 patients was 5 months(2∼21months+). Peripheral neuropathy was documented in 10
patients(45%). Bacterial infection was observed in 4 patients(1 spontaneous bacterial
peritonitis, 1 pneumonia, 1 sepsis, 1 bacteremia), of whom 2 patients died. Three patients
had mild Herpes zoster infection. Leukopenia and thrombocytopenia were observed in 8
and 2 patients, respectively.
Conclusion : These findings indicate that VAD regimen is effective for the refractory
multiple myeloma, especially for the secondary refractory multiple myeloma, but the
treatment related toxicities were serious.

Keywords Multiple myeloma, VAD chemotherapy, Vincristine, Doxorubicin, Dexamethasone

Article

Korean J Hematol 1996; 31(1): 145-153

Published online March 31, 1996

Copyright © The Korean Society of Hematology.

불응성 다발성 골수종 환자에 대한 VAD(Vincristine, Doxorubicin, Dexamethasone) 복합화학요법의 제 2상 임상연구

이종태, 김인호, 안진석, 이기형, 김태유, 박영이, 김효수, 허대석, 방영주

서울대학교 의과대학 내과학교실

Phase Ⅱ Trial of VAD (Vincristine, doxorubicin, and Dexamethasone) in Refractory Multiple Myeloma

Jong Tae Lee, In Ho Kim, Jin Seok Ahn, Ki Hyeong Lee, Tae Yu Kim, Young I Park, Hyo Soo Kim, Dae Seog Heo, Yung, Jue Bang, Seonyang Park, Byoung Kook Kim, Noe Kyeong Kim

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea

Abstract

Background : Multiple myeloma(MM) remains as an incurable malignant disorder as a
result of resistance to chemotherapy. With standard dose of alkylating agents such as
melphalan and prednisone (MP) or alkylating agent combinations with or without
doxorubicin, responses are achieved in approximately 50% of patients, and relapse
typically ensues after a median of 18 months. Therefore, salvage therapy becomes
important for half of the patients with newly diagnosed MM who fail to achieve
remission(primary refractory) and for responders who have a relapse despite
myelosuppressive doses of chemotherapy(secondary refractory). The VAD regimen,
comprising vincristine and doxorubicin given by continuous infusion along with high
doses of dexamethasone has achieved a marked tumor reduction in about one half of
patients. So we investigated the efficacy of VAD regimen for patients with refractory
multiple myeloma.
Methods: Twenty-two patients with refractory multiple myeloma were treated
according to the VAD protocols proposed by Barlogie et al.
Results: Of the 21 evaluable patients who completed at least one course of therapy, 9
had a complete response(43%). The response rates were 23% for primary refractory
disease patients and 75% for those with secondary refractory disease(P<0.05). The
median duration of response was 3 months(2∼18months) and the median survival for all
22 patients was 5 months(2∼21months+). Peripheral neuropathy was documented in 10
patients(45%). Bacterial infection was observed in 4 patients(1 spontaneous bacterial
peritonitis, 1 pneumonia, 1 sepsis, 1 bacteremia), of whom 2 patients died. Three patients
had mild Herpes zoster infection. Leukopenia and thrombocytopenia were observed in 8
and 2 patients, respectively.
Conclusion : These findings indicate that VAD regimen is effective for the refractory
multiple myeloma, especially for the secondary refractory multiple myeloma, but the
treatment related toxicities were serious.

Keywords: Multiple myeloma, VAD chemotherapy, Vincristine, Doxorubicin, Dexamethasone

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