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10.1155/2016/6848902

http://scihub22266oqcxt.onion/10.1155/2016/6848902
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C4753325!4753325!26949704
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suck abstract from ncbi


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pmid26949704      Biomed+Res+Int 2016 ; 2016 (ä): ä
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  • Efficacy and Safety of Novel Agent-Based Therapies for Multiple Myeloma: A Meta-Analysis #MMPMID26949704
  • Wang X; Li Y; Yan X
  • Biomed Res Int 2016[]; 2016 (ä): ä PMID26949704show ga
  • This study aimed at comparing bortezomib, thalidomide, and lenalidomide in patients with multiple myeloma (MM) for safety and efficacy using meta-analysis. This meta-analysis identified 17 randomized controlled trials (RCTs) including 6742 patients. These RCTs were separated according to the different agent-based regimens and to autologous stem-cell transplantation (ASCT). Complete response (CR), progression-free survival (PFS), overall survival (OS), and adverse events (AE) were combined. The total weighted risk ratio (RR) of CR was 3.29 [95% confidence interval (95% CI): 2.22?4.88] (P < 0.0001) for the novel agent-based regimens. These novel agent-based regimens showed greater benefit in terms of PFS of all subgroups irrespective of whether the patient received ASCT or not. The hazard ratio (HR) for PFS was 0.64 [95% CI: 0.60?0.69] (P < 0.00001). Improvements of OS could be found only in the bortezomib- and thalidomide-based regimens without ASCT. The pooled HRs were 0.74 [95% CI: 0.65?0.86] (P < 0.0001) and 0.80 [95% CI: 0.70?0.90] (P = 0.0004), respectively. Several AEs were shown more frequently in the novel agent-based regimens compared with controls such as hematologic events (neutropenia, anemia, and thrombocytopenia), gastrointestinal infection, peripheral neuropathy, thrombosis, and embolism events. In conclusion, in spite of the AEs, novel agent-based regimens are safe and effective for the treatment of MM.
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