Journal of Clinical Oncology, Vol 21, Issue 14
(July), 2003: 2732-2739
© 2003 American Society for Clinical Oncology
DTPACE: An Effective, Novel Combination Chemotherapy With Thalidomide for Previously Treated Patients With Myeloma
Choon-Kee Lee,
Bart Barlogie,
Nikhil Munshi,
Maurizio Zangari,
Athanasios Fassas,
Joth Jacobson,
Frits van Rhee,
Michele Cottler-Fox,
Firas Muwalla,
Guido Tricot
From The Myeloma Institute for Research and Therapy, The University of Arkansas for Medical Sciences, Little Rock, AR; Jerome Lipper Multiple Myeloma Center, Department of Adult Oncology, Dana Farber Cancer Institute, Boston, MA; Cancer Research and Biostatistics, Seattle, WA.
Address reprint requests to Choon-Kee Lee, MD, The Myeloma Institute for Research and Therapy, The University of Arkansas for Medical Sciences, Slot 776, 4301 West Markham, Little Rock, AR 72205; email: leechoonkee{at}uams.edu.
Purpose: To improve outcome in previously treated patients (at least two cycles of standard therapy) with multiple myeloma, thalidomide was combined with cytotoxic chemotherapy as induction therapy.
Patients and Methods: The regimen consisted of 4-days of oral dexamethasone, daily thalidomide, and 4 days of continuous-infusion cisplatin, doxorubicin, cyclophosphamide, and etoposide (DTPACE). Response to two cycles of DTPACE for induction was evaluated in 236 patients. Before being treated with DTPACE, 148 patients (63%) had shown progressive disease while receiving standard chemotherapy, and 55 patients (23%) had chromosome 13 abnormalities.
Results: The partial remission rate (PR) after two cycles of DTPACE was 32%, with 16% attaining a complete remission (CR) or near-CR (nCR; defined as only immunofixation electrophoresispositive). Patients with high lactate dehydrogenase (LDH; n = 98) showed a better response than those with normal LDH (n = 138): PR or better, 43% v 27% (P = .01); CR + nCR, 25% v 11% (P = .01). Patients with chromosome 13 abnormalities (n = 55) responded equally well as the other patients (n = 181): PR or better, 35% v 33% (P = .84); CR + nCR, 17% v 15% (P = .73). Patients who received 100% dose of DTPACE for two cycles (n = 115) achieved higher response rates than those with less than 100% dose (n = 121): PR or better, 49% v 17% (P < .0001); CR + nCR, 27% v 6% (P < .0001).
Conclusion: Combination therapy of oral dexamethasone and thalidomide with infusional chemotherapy is effective as induction therapy before autotransplantation, especially in patients with high-risk features.

CiteULike Complore Connotea Del.icio.us Digg Facebook Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
A. A Saad, M. Sharma, and G. M Higa
Treatment of Multiple Myeloma in the Targeted Therapy Era
Ann. Pharmacother.,
February 1, 2009;
43(2):
329 - 338.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Tricot, B. Barlogie, M. Zangari, F. van Rhee, A. Hoering, J. Szymonifka, and M. Cottler-Fox
Mobilization of peripheral blood stem cells in myeloma with either pegfilgrastim or filgrastim following chemotherapy
Haematologica,
November 1, 2008;
93(11):
1739 - 1742.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. San-Miguel, J.-L. Harousseau, D. Joshua, and K. C. Anderson
Individualizing Treatment of Patients With Myeloma in the Era of Novel Agents
J. Clin. Oncol.,
June 1, 2008;
26(16):
2761 - 2766.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Q. Bashir, C.-K. Lee, R. W. Stuart, M. L. Smith, J. Ryder, and R. Gonzalez
Phenotypic Evolution of Waldenstrom's Macroglobulinemia to Extramedullary Plasmacytoma
J. Clin. Oncol.,
May 10, 2008;
26(14):
2408 - 2410.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Manochakian, K. C. Miller, and A. A. Chanan-Khan
Clinical Impact of Bortezomib in Frontline Regimens for Patients with Multiple Myeloma
Oncologist,
August 1, 2007;
12(8):
978 - 990.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Barlogie, G. Tricot, E. Anaissie, J. Shaughnessy, E. Rasmussen, F. van Rhee, A. Fassas, M. Zangari, K. Hollmig, M. Pineda-Roman, et al.
Thalidomide and Hematopoietic-Cell Transplantation for Multiple Myeloma
N. Engl. J. Med.,
March 9, 2006;
354(10):
1021 - 1030.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Tricot, M. Reiner, M. Burns, M. Zangari, F. van Rhee, B. Barlogie, and M. Cottler-Fox
Mobilization of Stem Cells with DT-PACE Plus Pegfilgrastim vs. DT-PACE Plus Filgrastim in Previously Treated MM Patients.
Blood (ASH Annual Meeting Abstracts),
November 16, 2005;
106(11):
1972 - 1972.
[Abstract]
|
 |
|

|
 |

|
 |
 
A. Z. Badros, O. Goloubeva, A. P. Rapoport, B. Ratterree, N. Gahres, B. Meisenberg, N. Takebe, M. Heyman, J. Zwiebel, H. Streicher, et al.
Phase II Study of G3139, a Bcl-2 Antisense Oligonucleotide, in Combination With Dexamethasone and Thalidomide in Relapsed Multiple Myeloma Patients
J. Clin. Oncol.,
June 20, 2005;
23(18):
4089 - 4099.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
V. Eleutherakis-Papaiakovou, A. Bamias, and M. A. Dimopoulos
Thalidomide in cancer medicine
Ann. Onc.,
August 1, 2004;
15(8):
1151 - 1160.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Barlogie, J. Shaughnessy, G. Tricot, J. Jacobson, M. Zangari, E. Anaissie, R. Walker, and J. Crowley
Treatment of multiple myeloma
Blood,
January 1, 2004;
103(1):
20 - 32.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. A. Dimopoulos, A. Anagnostopoulos, and D. Weber
Treatment of Plasma Cell Dyscrasias With Thalidomide and Its Derivatives
J. Clin. Oncol.,
December 1, 2003;
21(23):
4444 - 4454.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|