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Blood, 2 April 2009, Vol. 113, No. 14, pp. 3383-3391.
Prepublished online as a Blood First Edition Paper on November 17, 2008; DOI 10.1182/blood-2008-07-170746.


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Submitted July 28, 2008
Accepted November 9, 2008

Long-term outcome of patients with multiple myeloma after autologous hematopoietic cell transplantation and nonmyeloablative allografting

Marcello Rotta, Barry E Storer, Firoozeh Sahebi, Judith A. Shizuru, Benedetto Bruno, Thoralf Lange, Edward D. Agura, Peter A. McSweeney, Michael A Pulsipher, Parameswaran Hari, Richard T. Maziarz, Thomas R. Chauncey, Frederick R. Appelbaum, Mohamed L. Sorror, William Bensinger, Brenda M. Sandmaier, Rainer F. Storb, and David G. Maloney*

Fred Hutchinson Cancer Research Center, Seattle, WA, United States
University of Washington, Seattle, WA, United States
City Of Hope National Medical Center/So. California Kaiser Permanente Medical Group, Duarte, CA, United States
Stanford University, Stanford, CA, United States
University of Torino, Torino, Italy
University of Leipzig, Leipzig, Germany
Baylor University, Waco, TX, United States
Rocky Mountain Cancer Center, Denver, CO, United States
University of Utah, Salt Lake City, UT, United States
Medical College of Wisconsin, Milwaukee, WI, United States
Oregon Health & Science University, Portland, OR, United States
Puget Sound VA Medical Center, Seattle, WA, United States

* Corresponding author; email: dmaloney{at}fhcrc.org.

Autologous hematopoietic cell transplantation (HCT) followed by nonmyeloablative allogeneic HCT (Auto/AlloHCT) provides cytoreduction and graft-versus-myeloma effects. We report on long-term outcomes of 102 patients with multiple myeloma who received Auto/AlloHCT with a median follow-up of 6.3 years. Treatment consisted of high-dose melphalan and autograft followed by 2 Gy total body irradiation, ± fludarabine and AlloHCT from HLA-identical siblings. Postgrafting immunosuppression was cyclosporine or tacrolimus and mycophenolate mofetil. Forty-two percent of patients developed grade 2-4 acute graft-versus-host-disease (GVHD) and 74% extensive chronic GVHD. Five-year non-relapse mortality after allografting was 18%, 95% related to GVHD or infections. Among 95 patients with detectable disease, 59 achieved complete remissions. Median time to progression was 5 years. Median overall survival (OS) was not reached. Median progression-free survival (PFS) was 3 years. Five-year OS and PFS were 64% and 36%, respectively. Seventy-three patients receiving AutoHCT within 10 months from treatment initiation had 5-year OS of 69% and PFS of 37%. In multivariate analysis, beta-2-microglobulin >3.5 µg/mL at diagnosis and Auto/AlloHCT >10 months after treatment initiation correlated with shorter OS (p=0.03 and p=0.02) and PFS (p=0.04 and p=0.03), while Karnofsky scores <90% at allotransplant correlated with shorter PFS only (p=0.005). Long-term disease control and GVHD remain key issues.


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Related Article in Blood Online:

Reduced-intensity allogeneic transplantation for myeloma: reality bites
A. Keith Stewart
Blood 2009 113: 3135-3136. [Full Text] [PDF]



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A. K. Stewart
Reduced-intensity allogeneic transplantation for myeloma: reality bites
Blood, April 2, 2009; 113(14): 3135 - 3136.
[Full Text] [PDF]



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