TY - JOUR
T1 - Seven-year median time to progression with thalidomide for smoldering myeloma
T2 - Partial response identifies subset requiring earlier salvage therapy for symptomatic disease
AU - Barlogie, Bart
AU - Van Rhee, Frits
AU - Shaughnessy, John D.
AU - Epstein, Joshua
AU - Yaccoby, Shmuel
AU - Pineda-Roman, Mauricio
AU - Hollmig, Klaus
AU - Alsayed, Yazan
AU - Hoering, Antje
AU - Szymonifka, Jackie
AU - Anaissie, Elias
AU - Petty, Nathan
AU - Kumar, Naveen S.
AU - Srivastava, Geetika
AU - Jenkins, Bonnie
AU - Crowley, John
AU - Zeldis, Jerome B.
PY - 2008/10/15
Y1 - 2008/10/15
N2 - Smoldering multiple myeloma (SMM) is usually followed expectantly without therapy. We conducted a phase 2 trial in 76 eligible patients with SMM, combining thalidomide (THAL, 200 mg/d) with monthly pamidronate. In the first 2 years, THAL dose reduction was required in 86% and drug was discontinued in 50%. Within 4 years, 63% improved, including 25% qualifying for partial response (PR); by then, 34 patients had progressed and 17 required salvage therapy. Unexpectedly, attaining PR status was associated with a shorter time to salvage therapy for disease progression (P<.001), perhaps reflecting greater drug sensitivity of more aggressive disease. Low beta-2-microglobulin levels less than 2 mg/L were independently associated with superior overall and event-free survival. Four-year survival and event-free survival estimates of 91% and 60%, respectively, together with a median postsalvage therapy survival of more than 5 years justify the conduct of a prospective randomized clinical trial to determine the clinical value of preemptive therapy in SMM. Trial registered at http://www.clinicaltrials.gov under identifier NCT00083382.
AB - Smoldering multiple myeloma (SMM) is usually followed expectantly without therapy. We conducted a phase 2 trial in 76 eligible patients with SMM, combining thalidomide (THAL, 200 mg/d) with monthly pamidronate. In the first 2 years, THAL dose reduction was required in 86% and drug was discontinued in 50%. Within 4 years, 63% improved, including 25% qualifying for partial response (PR); by then, 34 patients had progressed and 17 required salvage therapy. Unexpectedly, attaining PR status was associated with a shorter time to salvage therapy for disease progression (P<.001), perhaps reflecting greater drug sensitivity of more aggressive disease. Low beta-2-microglobulin levels less than 2 mg/L were independently associated with superior overall and event-free survival. Four-year survival and event-free survival estimates of 91% and 60%, respectively, together with a median postsalvage therapy survival of more than 5 years justify the conduct of a prospective randomized clinical trial to determine the clinical value of preemptive therapy in SMM. Trial registered at http://www.clinicaltrials.gov under identifier NCT00083382.
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U2 - 10.1182/blood-2008-06-164228
DO - 10.1182/blood-2008-06-164228
M3 - Article
C2 - 18669874
AN - SCOPUS:54049130077
SN - 0006-4971
VL - 112
SP - 3122
EP - 3125
JO - Blood
JF - Blood
IS - 8
ER -