scholarly journals 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

2021 ◽  
Author(s):  
Yuka Kawaji‐Kanayama ◽  
Tsutomu Kobayashi ◽  
Ayako Muramatsu ◽  
Hitoji Uchiyama ◽  
Nana Sasaki ◽  
...  
2020 ◽  
Vol 63 (5) ◽  
pp. 211
Author(s):  
Po-Nan Wang ◽  
Chieh-LinJerry Teng ◽  
Tran-Der Tan ◽  
Ying-Chung Hong ◽  
Sin-Syue Li ◽  
...  

2014 ◽  
Vol 38 (7) ◽  
pp. 788-794 ◽  
Author(s):  
Adam Walter-Croneck ◽  
Norbert Grzasko ◽  
Maria Soroka-Wojtaszko ◽  
Artur Jurczyszyn ◽  
Tigran Torosian ◽  
...  

2019 ◽  
Vol 9 (10) ◽  
Author(s):  
Cinnie Yentia Soekojo ◽  
Kihyun Kim ◽  
Shang-Yi Huang ◽  
Chor-Sang Chim ◽  
Naoki Takezako ◽  
...  

Abstract Pomalidomide is a third generation immunomodulatory drug which in combination with dexamethasone, has been shown to be active in relapsed/refractory multiple myeloma. However, the data in Asian patients remain limited. We conducted a prospective phase two clinical trial in major cancer centers in Singapore, South Korea, Taiwan, Japan and Hong Kong to assess the efficacy and safety of pomalidomide and dexamethasone combination (PomDex) +/− cyclophosphamide in Asian patients with relapsed/refractory multiple myeloma who failed lenalidomide and bortezomib. Patients were treated with pomalidomide (4 mg daily for 21 days every 4 weeks) and dexamethasone (40 mg weekly). If there is less than a minimal response after three cycles of PomDex, cyclophosphamide 300 mg/m2 can be added (PomCyDex). A total of 136 patients were enrolled. The median PFS was 9 and 10.8 months for the PomDex and PomCyDex group, respectively. The median OS was 16.3 months. This regimen appears to be active across age groups and prior lines of treatment. This combination was overall well tolerated with grade 3 and 4 adverse events of mainly cytopenias. PomDex is highly active and well-tolerated in Asian patients. The addition of cyclophosphamide can improve the response and outcomes further in patients with suboptimal response to PomDex.


2013 ◽  
Vol 31 (15_suppl) ◽  
pp. e19531-e19531
Author(s):  
Dipanjan Panda ◽  
Atul Sharma ◽  
Vinod Raina ◽  
Lalit Kumar ◽  
Renu Saxena ◽  
...  

e19531 Background: Venous thromboembolism (VTE) is a major complication of Multiple myeloma. The exact cause of thrombosis, role of anti myeloma drugs especially immunomodulators and steroids and the relation of thrombosis with alteration of thrombotic profile is not clear. While some available data is suggestive of low incidence of VTE in Asian population, true incidence and risk factors of VTE in Indian population is not known.So the present study was undertaken to have an evaluation of prothrombotic factors in Indian population. Methods: A prospective observational study was conducted from July 2008 to November 2009 at All India Institute of Medical Sciences (AIIMS), New Delhi, India. Thirty patients of newly diagnosed myeloma were recruited and were treated with thalidomide and dexamethasone for 4 months. Prothrombotic profile including protein Cand S, activated protein C resistance, plasma fibrinogen, factor VII and von Willebrand factor level was measured and Doppler study was done at baseline and after 4 months. Statistical analysis was done using SPSS 15 software. Frequency distribution, mean, median, range, standard deviation, Inter Quartile Range were calculated. To find out difference between pre and post treatment, Macnemar chi-square test (for proportion) and paired t test (mean) were done. Results: At the base line 4 patients (13%) had low protein C, 3 (10 %) had low protein S and 2 patients (6%) had high factor VIII. Post induction therapy 7 patients showed low protein C, 1 had low protein S and 1 had high factor VIII value. Rest of the factors was within normal limit both at baseline and post treatment in other patients. During the study period 2 subjects developed DVT. While one had low protein S, other patient had low protein C and low anti thrombin III which was done to find out the cause of DVT. Conclusions: Incidence of DVT in our patients seems to be less than western published data. Although thrombotic factors abnormalities are present in myeloma patients but the relation of coagulation factor abnormalities and development of DVT require further study. A larger prospective trial may be required to get a clear picture.


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