A modified regimen of pegylated liposomal doxorubicin, bortezomib and dexamethasone (DVD) is effective and well tolerated for previously untreated multiple myeloma patients

被引:25
作者
Berenson, James R. [1 ]
Yellin, Ori
Chen, Chien-Shing [2 ]
Patel, Ravi [3 ]
Bessudo, Alberto [4 ]
Boccia, Ralph V. [5 ]
Yang, Hank H.
Vescio, Robert [6 ]
Yung, Elizabeth
Mapes, Russell
Eades, Benjamin
Hilger, James D.
Wirtschafter, Eric [7 ]
Hilger, Jacqueline [8 ]
Nassir, Youram [9 ]
Swift, Regina A.
机构
[1] Inst Myeloma & Bone Canc Res, W Hollywood, CA 90069 USA
[2] Loma Linda Univ, Sch Med, Div Hematol & Oncol, Loma Linda, CA 92350 USA
[3] Comprehens Blood & Canc Ctr, Bakersfield, CA USA
[4] Pacific Oncol Hematol Associates, Encinitas, CA USA
[5] Ctr Canc & Blood Disorders, Bethesda, MD USA
[6] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[7] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[8] Millennium Pharmaceut Inc, Cambridge, MA USA
[9] Canc Care Inst, Los Angeles, CA USA
关键词
multiple myeloma; dexamethasone; bortezomib; pegylated liposomal doxorubicin; PHASE-III; THERAPY; COMBINATION; TRIAL; MULTICENTER; SENSITIVITY; RECURRENT; CANCER; CELLS;
D O I
10.1111/j.1365-2141.2011.08884.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The combination of pegylated liposomal doxorubicin (PLD), bortezomib and dexamethasone has shown efficacy in the treatment of multiple myeloma (MM) patients. Our earlier retrospective study suggested that modification of the doses, schedules and route of administration of these drugs appears to reduce toxicity without compromising anti-MM activity. As a result, we evaluated this modified drug combination in the frontline setting in a prospective multicentre phase II trial. Thirty-five previously untreated MM patients were enrolled. Dexamethasone IV 40 mg, bortezomib 1 mg/m(2) and PLD 5 mg/m(2) were administered on days 1, 4, 8 and 11 of a 4-week cycle. Patients were treated to their maximum response plus two additional cycles. The treatment regimen was discontinued after a maximum of eight cycles. Our modified schedule and dosing regimen achieved a high overall response rate of 86%, while showing a marked decrease in the incidence and severity of peripheral neuropathy, palmar-plantar erythrodysesthesia and myelo-suppression compared to the standard dosing on a 3-week cycle using these drugs. This modified regimen of dexamethasone, bortezomib and PLD shows improved tolerability and safety while maintaining a high response rate when compared to standard treatment with these agents in the frontline setting.
引用
收藏
页码:580 / 587
页数:8
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