| Literature DB >> 31867775 |
Wilson I Gonsalves1, Dragan Jevremovic2, Bharat Nandakumar1, Angela Dispenzieri1, Francis K Buadi1, David Dingli1, Martha Q Lacy1, Suzanne R Hayman1, Prashant Kapoor1, Nelson Leung1,3, Amie Fonder1, Miriam Hobbs1, Yi Lisa Hwa1, Eli Muchtar1, Rahma Warsame1, Taxiarchis V Kourelis1, Stephen Russell1, John A Lust1, Yi Lin1, Ronald S Go1, Mustaqeem A Siddiqui1, Robert A Kyle1, Morie A Gertz1, S Vincent Rajkumar1, Shaji K Kumar1.
Abstract
Our prior studies identified the prognostic significance of quantifying cPCs by multiparametric flow cytometry (MFC) in newly diagnosed multiple myeloma (NDMM) patients. We evaluated if a similar quantification of cPCs could add prognostic value to the current R-ISS classification of 556 consecutive NDMM patients seen at the Mayo Clinic, Rochester from 2009 to 2017. Those patients that had ≥5 cPCs/μL and either R-ISS stage I or stage II disease were re-classified as R-ISS IIB stage for the purposes of this study. The median time to next therapy (TTNT) and overall survival (OS) for patients with ≥5 cPCs/μL at diagnosis was as follows: R-ISS I (N = 110) - 40 months and not reached; R-ISS II (N = 69) - 30 and 72 months; R-ISS IIB (N = 96) - 21 and 45 months and R-ISS III (N = 281) - 20 and 47 months respectively. Finally, ≥ 5 cPCs/μL retained its adverse prognostic significance in a multivariable model for TTNT and OS. Hence, quantifying cPCs by MFC can potentially enhance the R-ISS classification of a subset of NDMM patients with stage I and II disease by identifying those patients with a worse than expected survival outcome.Entities:
Mesh:
Year: 2020 PMID: 31867775 PMCID: PMC7724649 DOI: 10.1002/ajh.25709
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047