PMID- 27760978 OWN - NLM STAT- MEDLINE DCOM- 20170503 LR - 20190606 IS - 1643-3750 (Electronic) IS - 1234-1010 (Print) IS - 1234-1010 (Linking) VI - 22 DP - 2016 Oct 20 TI - Efficacy and Safety of Danshen Compound Tablets in Preventing Thalidomide-Associated Thromboembolism in Patients with Multiple Myeloma: A Multicenter Retrospective Study. PG - 3835-3842 AB - BACKGROUND Currently available antithrombotic prophylaxis is not perfectly reliable in elderly patients. The aim of this retrospective study was to evaluate the efficacy and safety of Compound Danshen Tablet (CDT) in preventing thromboembolism in multiple myeloma (MM) patients treated with thalidomide-based regimens. MATERIAL AND METHODS MM patients treated with thalidomide-based regimens were retrospectively reviewed between January 2008 and March 2015. Patients were categorized into 3 cohorts based on thromboembolic prophylaxis used: CDT, Warfarin Tablet, and no prophylaxis. Venous thromboembolism (VTE), other adverse effects (AEs), and the changes of D-dimer and fibrinogen levels were monitored. RESULTS Seven out of 313 MM patients (2.24%) developed venous thrombosis events (VTE) in this retrospective study, all clustering in the no prophylaxis cohort. Three patients of the Warfarin cohort (3.19%) experienced hemorrhage. Neither VTE events nor serious AEs were observed in the CDT cohort. Following Compound Danshen or Warfarin treatment for 3 months, the D-dimer and fibrinogen levels (in particular the D-dimer level) (all P<0.05), were obviously decreased relative to their respective baselines and the no prophylaxis cohort. In contrast, the 2 blotting parameters were significantly increased in the no prophylaxis cohort relative to the baseline level (All P<0.05), and were even higher in the patients experiencing VTE compared to the no VTE patients (P<0.0001 and P=0.016, respectively). CONCLUSIONS Our findings indicate CDT is an effective therapy for preventing VTE in MM patients treated with thalidomide-based regimens, and is well tolerated in long-term use. FAU - Yin, Qing-Song AU - Yin QS AD - Department of Leukemia, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China (mainland). FAU - Chen, Lin AU - Chen L AD - Department of Leukemia, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China (mainland). FAU - Mi, Rui-Hua AU - Mi RH AD - Department of Leukemia, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China (mainland). FAU - Ai, Hao AU - Ai H AD - Department of Leukemia, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China (mainland). FAU - Yin, Jun-Jie AU - Yin JJ AD - Department of Leukemia, The Central Hospital of Xinxiang, Xinxiang, Henan, China (mainland). FAU - Liu, Xiao-Juan AU - Liu XJ AD - Department of Leukemia , The Second People's Hospital of Jiaozuo, Jiaozuo, Henan, China (mainland). FAU - Wei, Xu-Dong AU - Wei XD AD - Department of Leukemia , Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China (mainland). LA - eng PT - Journal Article PT - Multicenter Study DEP - 20161020 PL - United States TA - Med Sci Monit JT - Medical science monitor : international medical journal of experimental and clinical research JID - 9609063 RN - 0 (Anticoagulants) RN - 0 (Fibrin Fibrinogen Degradation Products) RN - 0 (Plant Preparations) RN - 0 (Tablets) RN - 0 (fibrin fragment D) RN - 4Z8R6ORS6L (Thalidomide) RN - 5Q7ZVV76EI (Warfarin) SB - IM MH - Adult MH - Aged MH - Anticoagulants/administration & dosage MH - Antineoplastic Combined Chemotherapy Protocols/adverse effects/therapeutic use MH - Female MH - Fibrin Fibrinogen Degradation Products/metabolism MH - Humans MH - Male MH - Middle Aged MH - Multiple Myeloma/*blood/*drug therapy MH - Phytotherapy MH - Plant Preparations/*therapeutic use MH - Retrospective Studies MH - Risk Factors MH - *Salvia miltiorrhiza MH - Tablets MH - Thalidomide/adverse effects MH - Venous Thromboembolism/blood/chemically induced/*prevention & control MH - Warfarin/administration & dosage PMC - PMC5077292 EDAT- 2016/10/21 06:00 MHDA- 2017/05/04 06:00 PMCR- 2016/10/20 CRDT- 2016/10/21 06:00 PHST- 2016/10/21 06:00 [pubmed] PHST- 2017/05/04 06:00 [medline] PHST- 2016/10/21 06:00 [entrez] PHST- 2016/10/20 00:00 [pmc-release] AID - 900575 [pii] AID - 10.12659/msm.900575 [doi] PST - epublish SO - Med Sci Monit. 2016 Oct 20;22:3835-3842. doi: 10.12659/msm.900575.