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      Prognostic impact of resistance to bortezomib and/or lenalidomide in carfilzomib‐based therapies for relapsed/refractory multiple myeloma: The Kyoto Clinical Hematology Study Group, multicenter, pilot, prospective, observational study in Asian patients

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          Abstract

          Background

          Combinatory strategies with carfilzomib (CFZ), a second‐generation proteasome inhibitor, plus dexamethasone (DEX) with or without lenalidomide (LEN) have shown promising efficacy for patients with relapsed/refractory multiple myeloma (RRMM) in pivotal clinical trials. However, their effects on patients who were resistance to bortezomib (BTZ) and/or LEN have not been fully evaluated in a daily practice setting.

          Aims

          To evaluate the real‐world efficacy and safety of CFZ‐based treatments; that is, CFZ with LEN plus DEX (KRD therapy) and CFZ with DEX (KD therapy), in Asian patients, we conducted a multicenter pilot prospective observational study in the Kyoto Clinical Hematology Study Group.

          Methods and Results

          All 50 patients with RRMM enrolled in this study were treated with CFZ‐based treatments between 2017 and 2019. KRD and KD were administered to 31 and 19 patients, respectively. The overall response rates (ORRs) were 80.6% with KRD and 73.7% with KD. Two‐year progression‐free survival (PFS) and overall survival (OS) were 58.5% and 79.7% with KRD, and 23.1% and 52.6% with KD. By multivariate analysis, refractoriness to BTZ and to LEN were identified as independent unfavorable factors for both PFS and OS. The common non‐hematologic AEs included hypertension (42.0%), fever (24.0%), fatigue (24.0%), and infection (16.0%). No serious heart failure was observed. This study is registered as UMIN000025108.

          Conclusion

          This study suggests the need of the development of novel CFZ‐containing strategy which can overcome the refractoriness to BTZ and/or LEN, while both KRD and KD were shown to be mostly feasible in Asian patients in a daily practice setting.

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          Most cited references43

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          Investigation of the freely available easy-to-use software ‘EZR' for medical statistics

          Y Kanda (2012)
          Although there are many commercially available statistical software packages, only a few implement a competing risk analysis or a proportional hazards regression model with time-dependent covariates, which are necessary in studies on hematopoietic SCT. In addition, most packages are not clinician friendly, as they require that commands be written based on statistical languages. This report describes the statistical software ‘EZR' (Easy R), which is based on R and R commander. EZR enables the application of statistical functions that are frequently used in clinical studies, such as survival analyses, including competing risk analyses and the use of time-dependent covariates, receiver operating characteristics analyses, meta-analyses, sample size calculation and so on, by point-and-click access. EZR is freely available on our website (http://www.jichi.ac.jp/saitama-sct/SaitamaHP.files/statmed.html) and runs on both Windows (Microsoft Corporation, USA) and Mac OS X (Apple, USA). This report provides instructions for the installation and operation of EZR.
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            Sample size of 12 per group rule of thumb for a pilot study

              • Record: found
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              International staging system for multiple myeloma.

              There is a need for a simple, reliable staging system for multiple myeloma that can be applied internationally for patient classification and stratification. Clinical and laboratory data were gathered on 10,750 previously untreated symptomatic myeloma patients from 17 institutions, including sites in North America, Europe, and Asia. Potential prognostic factors were evaluated by univariate and multivariate techniques. Three modeling approaches were then explored to develop a staging system including two nontree and one tree survival assessment methodologies. Serum beta2-microglobulin (Sbeta2M), serum albumin, platelet count, serum creatinine, and age emerged as powerful predictors of survival and were then used in the tree analysis approach. A combination of Sbeta2M and serum albumin provided the simplest, most powerful and reproducible three-stage classification. This new International Staging System (ISS) was validated in the remaining patients and consists of the following stages: stage I, Sbeta2M less than 3.5 mg/L plus serum albumin > or = 3.5 g/dL (median survival, 62 months); stage II, neither stage I nor III (median survival, 44 months); and stage III, Sbeta2M > or = 5.5 mg/L (median survival, 29 months). The ISS system was further validated by demonstrating effectiveness in patients in North America, Europe, and Asia; in patients less than and > or = 65 years of age; in patients with standard therapy or autotransplantation; and in comparison with the Durie/Salmon staging system. CONCLUSION) The new ISS is simple, based on easy to use variables (Sbeta2M and serum albumin), and recommended for early adoption and widespread use.

                Author and article information

                Contributors
                t-koba@koto.kpu-m.ac.jp
                Journal
                Cancer Rep (Hoboken)
                Cancer Rep (Hoboken)
                10.1002/(ISSN)2573-8348
                CNR2
                Cancer Reports
                John Wiley and Sons Inc. (Hoboken )
                2573-8348
                14 June 2021
                February 2022
                : 5
                : 2 ( doiID: 10.1002/cnr2.v5.2 )
                : e1476
                Affiliations
                [ 1 ] Division of Hematology and Oncology, Department of Medicine Kyoto Prefectural University of Medicine Kyoto Japan
                [ 2 ] Department of Hematology Japanese Red Cross Kyoto Daiichi Hospital Kyoto Japan
                [ 3 ] Department of Hematology Japanese Red Cross Kyoto Daini Hospital Kyoto Japan
                [ 4 ] Department of Internal Medicine Otsu Municipal Hospital Otsu Japan
                [ 5 ] Department of Hematology Omihachiman Community Medical Center Omihachiman Japan
                [ 6 ] Department of Hematology Aiseikai Yamashina Hospital Kyoto Japan
                [ 7 ] Department of Hematology Matsushita Memorial Hospital Moriguchi Japan
                [ 8 ] Department of Hematology Fukuchiyama City Hospital Fukuchiyama Japan
                [ 9 ] Department of Hematology, Japan Community Health care Organization Kyoto Kuramaguchi Medical Center Kyoto Japan
                [ 10 ] Center for Molecular Diagnostic and Therapeutics Kyoto Prefectural University of Medicine Kyoto Japan
                Author notes
                [*] [* ] Correspondence

                Tsutomu Kobayashi, Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, 465 Kajii‐cho, Kamigyo‐ku, Kyoto, 602‐8566, Japan.

                Email: t-koba@ 123456koto.kpu-m.ac.jp

                Author information
                https://orcid.org/0000-0002-5600-5762
                https://orcid.org/0000-0001-8966-2876
                https://orcid.org/0000-0001-6130-1550
                Article
                CNR21476
                10.1002/cnr2.1476
                8842705
                34124862
                a4726134-31e8-4254-9aa1-4b988ca34912
                © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 31 May 2021
                : 21 February 2021
                : 01 June 2021
                Page count
                Figures: 2, Tables: 3, Pages: 10, Words: 6915
                Funding
                Funded by: Ono Pharmaceutical Co., Ltd , doi 10.13039/501100013170;
                Categories
                Original Article
                Original Article
                Custom metadata
                2.0
                February 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.1 mode:remove_FC converted:14.02.2022

                bortezomib,carfilzomib,lenalidomide,multiple myeloma
                bortezomib, carfilzomib, lenalidomide, multiple myeloma

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