TY - JOUR
T1 - A modified regimen of pegylated liposomal doxorubicin, bortezomib and dexamethasone (DVD) is effective and well tolerated for previously untreated multiple myeloma patients
AU - Berenson, James R.
AU - Yellin, Ori
AU - Chen, Chien Shing
AU - Patel, Ravi
AU - Bessudo, Alberto
AU - Boccia, Ralph V.
AU - Yang, Hank H.
AU - Vescio, Robert
AU - Yung, Elizabeth
AU - Mapes, Russell
AU - Eades, Benjamin
AU - Hilger, James D.
AU - Wirtschafter, Eric
AU - Hilger, Jacqueline
AU - Nassir, Youram
AU - Swift, Regina A.
N1 - James R. Berenson, MD, Institute for Myeloma and Bone Cancer Research, 9201 W. Sunset Blvd., Suite 300, West Hollywood, CA 90069, USA. E‐mail: [email protected] The combination of pegylated liposomal doxorubicin (PLD), bortezomib and dexamethasone has shown efficacy in the treatment of multiple myeloma (MM) patients.
PY - 2011/12
Y1 - 2011/12
N2 - 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 40mg, bortezomib 1mg/m2 and PLD 5mg/m2 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 myelosuppression 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.
AB - 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 40mg, bortezomib 1mg/m2 and PLD 5mg/m2 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 myelosuppression 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.
KW - Bortezomib
KW - Dexamethasone
KW - Multiple myeloma
KW - Pegylated liposomal doxorubicin
UR - https://www.scopus.com/pages/publications/81155139575
UR - https://www.scopus.com/pages/publications/81155139575#tab=citedBy
U2 - 10.1111/j.1365-2141.2011.08884.x
DO - 10.1111/j.1365-2141.2011.08884.x
M3 - Article
C2 - 21950583
SN - 0007-1048
VL - 155
SP - 580
EP - 587
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 5
ER -