Seven-year median time to progression with thalidomide for smoldering myeloma: partial response identifies subset requiring earlier salvage therapy for symptomatic disease

被引:81
作者
Barlogie, Bart [1 ]
van Rhee, Frits [1 ]
Shaughnessy, John D., Jr. [1 ]
Epstein, Joshua [1 ]
Yaccoby, Shmuel [1 ]
Pineda-Roman, Mauricio [1 ]
Hollmig, Klaus [1 ]
Alsayed, Yazan [1 ]
Hoering, Antje [2 ]
Szymonifka, Jackie [2 ]
Anaissie, Elias [1 ]
Petty, Nathan [1 ]
Kumar, Naveen S. [1 ]
Srivastava, Geetika [1 ]
Jenkins, Bonnie [1 ]
Crowley, John [2 ]
Zeldis, Jerome B. [3 ]
机构
[1] Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
[2] Canc Res & Biostat, Seattle, WA USA
[3] Celgene, Summit, NJ USA
关键词
D O I
10.1182/blood-2008-06-164228
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:3122 / 3125
页数:4
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