TY - JOUR
T1 - Long-term outcome results of the first tandem autotransplant trial for multiple myeloma
AU - Barlogie, Bart
AU - Tricot, Guido J.
AU - Van Rhee, Frits
AU - Angtuaco, Edguardo
AU - Walker, Ron
AU - Epstein, Joshua
AU - Shaughnessy, John D.
AU - Jagannath, Sundar
AU - Bolejack, Vanessa
AU - Gurley, Jennifer
AU - Hoering, Antje
AU - Vesole, David
AU - Desikan, Raman
AU - Siegel, David
AU - Mehta, Jayesh
AU - Singhal, Seema
AU - Munshi, Nikhil C.
AU - Dhodapkar, Madhav
AU - Jenkins, Bonnie
AU - Attal, Michel
AU - Harousseau, Jean Luc
AU - Crowley, John
PY - 2006/10
Y1 - 2006/10
N2 - Total Therapy 1, the first tandem autotransplant trial for newly diagnosed patients with multiple myeloma, was designed to increase the frequency of complete response (CR) and thereby extend survival. With a median follow-up of 12 years, 62 of 231 initially enrolled patients are alive (17% at 15 years); 31 remain event free (7% at 15 years) including 16 of 94 (41%) that initially achieved CR. Currently alive patients less frequently had cytogenetic abnormalities (CAs) at baseline (P = 0.002), postenrolment (P < 0.001) and at relapse (P = 0.004); elevations of serum C-reactive protein (CRP) (P = 0.003) and lactate dehydrogenase (P = 0.029), anaemia (P = 0.029) and they more often completed two transplants within 12 months (P = 0.019). Postenrolment overall survival (OS) and event-free survival (EFS) were superior in the absence of CA of the hypodiploidy or deletion 13 variety (P < 0.001 and 0.037 respectively) and in the presence of low CRP at baseline (P = 0.001 and 0.017 respectively). Postrelapse survival was longer in the absence of CA at relapse (P < 0.001), IgA isotype (P = 0.002), International Staging System stage 3 (P = 0.014), and when patients had two protocol transplants prior to relapse (P = 0.038). Ten-year EFS and OS could be accomplished in 15% and 33% of patients, respectively, when all agents available in 1989, especially high-dose melphalan, were applied together upfront for the management of myeloma.
AB - Total Therapy 1, the first tandem autotransplant trial for newly diagnosed patients with multiple myeloma, was designed to increase the frequency of complete response (CR) and thereby extend survival. With a median follow-up of 12 years, 62 of 231 initially enrolled patients are alive (17% at 15 years); 31 remain event free (7% at 15 years) including 16 of 94 (41%) that initially achieved CR. Currently alive patients less frequently had cytogenetic abnormalities (CAs) at baseline (P = 0.002), postenrolment (P < 0.001) and at relapse (P = 0.004); elevations of serum C-reactive protein (CRP) (P = 0.003) and lactate dehydrogenase (P = 0.029), anaemia (P = 0.029) and they more often completed two transplants within 12 months (P = 0.019). Postenrolment overall survival (OS) and event-free survival (EFS) were superior in the absence of CA of the hypodiploidy or deletion 13 variety (P < 0.001 and 0.037 respectively) and in the presence of low CRP at baseline (P = 0.001 and 0.017 respectively). Postrelapse survival was longer in the absence of CA at relapse (P < 0.001), IgA isotype (P = 0.002), International Staging System stage 3 (P = 0.014), and when patients had two protocol transplants prior to relapse (P = 0.038). Ten-year EFS and OS could be accomplished in 15% and 33% of patients, respectively, when all agents available in 1989, especially high-dose melphalan, were applied together upfront for the management of myeloma.
KW - High-dose melphalan
KW - Myeloma
KW - Prognosis
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U2 - 10.1111/j.1365-2141.2006.06271.x
DO - 10.1111/j.1365-2141.2006.06271.x
M3 - Article
C2 - 16939489
AN - SCOPUS:33748748536
SN - 0007-1048
VL - 135
SP - 158
EP - 164
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -