Dexamethasone, cyclophosphamide, idarubicin and etoposide (DC-IE): A novel, intensive induction chemotherapy regimen for patients with high-risk multiple myeloma

被引:11
作者
Ballester, OF
Moscinski, LC
Fields, KK
Hiemenz, JW
Zorsky, PE
Goldstein, SC
Saba, HI
Spiers, ASD
Kronish, L
Sullivan, P
Elfenbein, GJ
机构
[1] UNIV S FLORIDA,H LEE MOFFITT CANC CTR & RES INST,DIV PATHOL,TAMPA,FL 33612
[2] UNIV S FLORIDA,H LEE MOFFITT CANC CTR & RES INST,DIV HEMATOL ONCOL,TAMPA,FL 33612
关键词
myeloma; induction chemotherapy; time sequenced; idarubicin; etoposide;
D O I
10.1046/j.1365-2141.1997.d01-2083.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We evaluated toxicities and responses to a novel, dose intensive and time sequenced, chemotherapy programme (DC-IE) in 45 patients with high-risk myeloma. DC-IE consisted of: dexamethasone (days 1-4); cyclophosphamide (day 5); idarubicin and etoposide (days 8-10). Complete response (CR) was achieved in four patients, six patients achieved near complete responses (nCR) and 21 patients achieved a partial remission (PR). Overall response rate was 76% (CI 56-94%) for newly diagnosed patients (n = 21) and 62% (CI 36-81%) for relapsed/refractory patients (n = 24). Toxicities were limited to myelosuppression; two patients died of sepsis during neutropenia (4%). DC-IE is active and tolerable for high-risk multiple myeloma, including patients with relapsed or refractory disease to anthracycline containing regimens.
引用
收藏
页码:746 / 748
页数:3
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