| Literature DB >> 25445028 |
Ravi Vij1, Shaji Kumar2, Mei-Jie Zhang3, Xiaobo Zhong4, Jiaxing Huang4, Angela Dispenzieri2, Muneer H Abidi5, Jennifer M Bird6, César O Freytes7, Robert Peter Gale8, Tamila L Kindwall-Keller9, Robert A Kyle2, Daniel J Landsburg10, Hillard M Lazarus11, Reinhold Munker12, Vivek Roy13, Manish Sharma14, Dan T Vogl10, Baldeep Wirk15, Parameswaran N Hari16.
Abstract
Patients with multiple myeloma (MM) who are eligible for autologous stem cell transplantation (ASCT) typically receive a finite period of initial therapy before ASCT. It is not clear if patients with suboptimal (less than a partial) response to initial therapy benefit from additional alternative therapy with intent to maximize pretransplant response. We identified 539 patients with MM who had an ASCT after having achieved less than a partial response (PR) to first-line induction chemotherapy between 1995 and 2010. These patients were then divided into 2 groups: those who received additional salvage chemotherapy before ASCT (n = 324) and those who had no additional salvage chemotherapy immediately before ASCT (n = 215). Additional pretransplant chemotherapy resulted in deepening responses in 68% (complete response in 8% and PR in 60%). On multivariate analysis there was no impact of pretransplant salvage chemotherapy on treatment-related mortality, risk for relapse, progression-free survival, or overall survival. In conclusion, for patients achieving less than a PR to initial induction therapy, including with novel agent combinations, additional pre-ASCT salvage chemotherapy improved the depth of response and pre-ASCT disease status but was not associated with survival benefit.Entities:
Keywords: Autologous transplant; Myeloma; Primary refractory
Mesh:
Year: 2014 PMID: 25445028 PMCID: PMC4297511 DOI: 10.1016/j.bbmt.2014.10.023
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742