| Literature DB >> 23297129 |
A Keith Stewart1, Suzanne Trudel, Nizar J Bahlis, Darrell White, Waleed Sabry, Andrew Belch, Tony Reiman, Jean Roy, Chaim Shustik, Michael J Kovacs, Morel Rubinger, Guy Cantin, Kevin Song, Kirsty A Tompkins, Deb C Marcellus, Martha Q Lacy, Jonathan Sussman, Donna Reece, Michael Brundage, Erica L Harnett, Lois Shepherd, Judy-Anne W Chapman, Ralph M Meyer.
Abstract
We conducted a randomized, controlled trial comparing thalidomide-prednisone as maintenance therapy with observation in 332 patients who had undergone autologous stem cell transplantation with melphalan 200 mg/m2. The primary end point was overall survival (OS); secondary end points were myeloma-specific progression-free survival,progression-free survival, incidence of venous thromboembolism, and health-related quality of life (HRQoL). With a median follow-up of 4.1 years, no differences in OS between thalidomide-prednisone and observation were detected (respective 4-year estimates of 68% vs 60%, respectively; hazard ratio = 0.77; P = .18); thalidomide-prednisone was associated with superior myeloma-specific progression-free survival and progression-free survival (for both outcomes, the 4-year estimates were 32% vs 14%; hazard ratio = 0.56; P < .0001) and more frequent venous thromboembolism (7.3% vs none; P = .0004). Median survival after first disease recurrence was 27.7 months with thalidomide-prednisone and 34.1 months in the observation group. Nine second malignancies were observed with thalidomide-prednisone versus 6 in the observation group. Those allocated to thalidomide-prednisone reported worse HRQoL with respect to cognitive function, dyspnea, constipation, thirst, leg swelling, numbness, dry mouth, and balance problems. We conclude that maintenance therapy with thalidomide-prednisone after autologous stem cell transplantation improves the duration of disease control, but is associated with worsening of patient-reported HRQoL and no detectable OS benefit.Entities:
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Year: 2013 PMID: 23297129 PMCID: PMC3587317 DOI: 10.1182/blood-2012-09-451872
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113