0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Prognostic impact of rapid reduction of involved free light chains in multiple myeloma patients under first-line treatment with Bendamustine, Prednisone, and Bortezomib (BPV)

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Introduction

          Light chain involvement is observed in almost every patient (pt) with newly diagnosed multiple myeloma (MM). Owing to a relatively short half-life, rapid reduction in the involved free light chain (iFLC) is of potential prognostic value.

          Methods

          This retrospective analysis included 92 pts with newly diagnosed MM treated with bendamustine, prednisone, and bortezomib (BPV).

          Results

          After a median number of two (range 1–5) BPV cycles, the majority of pts ( n = 86; 93%) responded with either sCR ( n = 21), CR ( n = 1), nCR ( n = 25), VGPR ( n = 20), or PR ( n = 19). PFS and OS at 48 months were 39% and 67%, respectively. At baseline, 79 out of 92 pts (86%) had iFLC levels above the upper standard level and an abnormal ratio of involved to uninvolved free light chain ≥ 8. In a subgroup analysis of these pts, we evaluated the prognostic importance of an early reduction of the iFLC during the first two BPV cycles. A reduction ≥ 50% of the iFLC on day 8 of the first cycle was observed in 31 of 69 pts. These pts had a significantly better median PFS of 49 months as compared to 20 months in 38 pts with a lower iFLC reduction ( p = 0.002). In contrast, OS did not differ significantly with a 48 months survival of 77% vs 69% ( p > 0.05).

          Conclusion

          These results indicate that a rapid decrease in the iFLC on day 8 is an early prognostic marker for newly diagnosed MM pts undergoing BPV treatment.

          Related collections

          Most cited references32

          • Record: found
          • Abstract: found
          • Article: not found

          International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma.

          This International Myeloma Working Group consensus updates the disease definition of multiple myeloma to include validated biomarkers in addition to existing requirements of attributable CRAB features (hypercalcaemia, renal failure, anaemia, and bone lesions). These changes are based on the identification of biomarkers associated with near inevitable development of CRAB features in patients who would otherwise be regarded as having smouldering multiple myeloma. A delay in application of the label of multiple myeloma and postponement of therapy could be detrimental to these patients. In addition to this change, we clarify and update the underlying laboratory and radiographic variables that fulfil the criteria for the presence of myeloma-defining CRAB features, and the histological and monoclonal protein requirements for the disease diagnosis. Finally, we provide specific metrics that new biomarkers should meet for inclusion in the disease definition. The International Myeloma Working Group recommends the implementation of these criteria in routine practice and in future clinical trials, and recommends that future studies analyse any differences in outcome that might occur as a result of the new disease definition.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group.

            Serum creatinine concentration is widely used as an index of renal function, but this concentration is affected by factors other than glomerular filtration rate (GFR). To develop an equation to predict GFR from serum creatinine concentration and other factors. Cross-sectional study of GFR, creatinine clearance, serum creatinine concentration, and demographic and clinical characteristics in patients with chronic renal disease. 1628 patients enrolled in the baseline period of the Modification of Diet in Renal Disease (MDRD) Study, of whom 1070 were randomly selected as the training sample; the remaining 558 patients constituted the validation sample. The prediction equation was developed by stepwise regression applied to the training sample. The equation was then tested and compared with other prediction equations in the validation sample. To simplify prediction of GFR, the equation included only demographic and serum variables. Independent factors associated with a lower GFR included a higher serum creatinine concentration, older age, female sex, nonblack ethnicity, higher serum urea nitrogen levels, and lower serum albumin levels (P < 0.001 for all factors). The multiple regression model explained 90.3% of the variance in the logarithm of GFR in the validation sample. Measured creatinine clearance overestimated GFR by 19%, and creatinine clearance predicted by the Cockcroft-Gault formula overestimated GFR by 16%. After adjustment for this overestimation, the percentage of variance of the logarithm of GFR predicted by measured creatinine clearance or the Cockcroft-Gault formula was 86.6% and 84.2%, respectively. The equation developed from the MDRD Study provided a more accurate estimate of GFR in our study group than measured creatinine clearance or other commonly used equations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              International uniform response criteria for multiple myeloma.

              New uniform response criteria are required to adequately assess clinical outcomes in myeloma. The European Group for Blood and Bone Marrow Transplant/International Bone Marrow Transplant Registry criteria have been expanded, clarified and updated to provide a new comprehensive evaluation system. Categories for stringent complete response and very good partial response are added. The serum free light-chain assay is included to allow evaluation of patients with oligo-secretory disease. Inconsistencies in prior criteria are clarified making confirmation of response and disease progression easier to perform. Emphasis is placed upon time to event and duration of response as critical end points. The requirements necessary to use overall survival duration as the ultimate end point are discussed. It is anticipated that the International Response Criteria for multiple myeloma will be widely used in future clinical trials of myeloma.
                Bookmark

                Author and article information

                Contributors
                Wolfram.Poenisch@medizin.uni-leipzig.de
                Journal
                J Cancer Res Clin Oncol
                J Cancer Res Clin Oncol
                Journal of Cancer Research and Clinical Oncology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0171-5216
                1432-1335
                12 January 2021
                12 January 2021
                2021
                : 147
                : 8
                : 2349-2359
                Affiliations
                [1 ]GRID grid.411339.d, ISNI 0000 0000 8517 9062, Hematology and Cell Therapy, , Medical Clinic and Policlinic 1, University Hospital Leipzig, ; Liebigstraße 22, 04103 Leipzig, Germany
                [2 ]Hospital Torgau, Christianistraße 1, 04860 Torgau, Germany
                [3 ]GRID grid.491873.0, ISNI 0000 0000 9466 4668, HELIOS Vogtland - Klinikum Plauen, ; Röntgenstraße 2, 08529 Plauen, Germany
                [4 ]Hematology Practice, Biedermannstraße 84, 04277 Leipzig, Germany
                [5 ]Hematology Practice, Strümpellstraße 42, 04289 Leipzig, Germany
                [6 ]Medical Care Center Schöneck, Albertplatz 1, 08261 Schöneck, Germany
                [7 ]Hematology Practice, Lütznerstraße 162, 04179 Leipzig, Germany
                [8 ]Hematology Practice, Theodor - Heuss-Str. 2, 04435 Schkeuditz, Germany
                [9 ]GRID grid.9647.c, ISNI 0000 0004 7669 9786, Clinic Pharmacy, , University of Leipzig, ; Liebigstraße 20, 04103 Leipzig, Germany
                [10 ]GRID grid.9647.c, ISNI 0000 0004 7669 9786, Institute for Medical Informatics, Statistics and Epidemiology (IMISE), , University of Leipzig, ; Härtelstraße 16-18, 04107 Leipzig, Germany
                Author information
                http://orcid.org/0000-0002-9666-6274
                Article
                3504
                10.1007/s00432-020-03504-3
                8236483
                33433659
                bd8a37d6-990e-4347-a9c6-60174cd017ad
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 16 September 2020
                : 12 December 2020
                Funding
                Funded by: Projekt DEAL
                Categories
                Original Article – Clinical Oncology
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2021

                Oncology & Radiotherapy
                multiple myeloma,involved free light chain,first-line treatment,bendamustine,bortezomib

                Comments

                Comment on this article