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Derivation and Validation of a Risk Assessment Model for Immunomodulatory Drug-Associated Thrombosis Among Patients With Multiple Myeloma.多发性骨髓瘤患者免疫调节药物相关血栓形成风险评估模型的推导和验证。
J Natl Compr Canc Netw. 2019 Jul 1;17(7):840-847. doi: 10.6004/jnccn.2018.7273.
2
Preventing Venous Thromboembolism in Patients with Cancer. Reply.癌症患者静脉血栓栓塞的预防。回复。
N Engl J Med. 2019 May 30;380(22):2181. doi: 10.1056/NEJMc1904003.
3
Carfilzomib or bortezomib with melphalan-prednisone for transplant-ineligible patients with newly diagnosed multiple myeloma.卡非佐米或硼替佐米联合马法兰-泼尼松用于不适合移植的新诊断多发性骨髓瘤患者。
Blood. 2019 May 2;133(18):1953-1963. doi: 10.1182/blood-2018-09-874396. Epub 2019 Feb 28.
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Direct Oral Anticoagulants for Thromboprophylaxis in Ambulatory Patients with Cancer.直接口服抗凝剂用于门诊癌症患者的血栓预防
N Engl J Med. 2019 Feb 21;380(8):781-783. doi: 10.1056/NEJMe1816060.
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Rivaroxaban for Thromboprophylaxis in High-Risk Ambulatory Patients with Cancer.利伐沙班预防高风险门诊癌症患者血栓栓塞症。
N Engl J Med. 2019 Feb 21;380(8):720-728. doi: 10.1056/NEJMoa1814630.
6
Apixaban to Prevent Venous Thromboembolism in Patients with Cancer.阿哌沙班预防癌症患者静脉血栓栓塞症。
N Engl J Med. 2019 Feb 21;380(8):711-719. doi: 10.1056/NEJMoa1814468. Epub 2018 Dec 4.
7
Validation of body mass index (BMI)-related ICD-9-CM and ICD-10-CM administrative diagnosis codes recorded in US claims data.验证美国索赔数据中与体重指数(BMI)相关的 ICD-9-CM 和 ICD-10-CM 行政诊断代码。
Pharmacoepidemiol Drug Saf. 2018 Oct;27(10):1092-1100. doi: 10.1002/pds.4617. Epub 2018 Jul 12.
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A phase I/II dose-escalation study investigating all-oral ixazomib-melphalan-prednisone induction followed by single-agent ixazomib maintenance in transplant-ineligible newly diagnosed multiple myeloma.一项 I/II 期剂量递增研究,旨在评估不适合移植的新诊断多发性骨髓瘤患者中,全口服伊沙佐米-美法仑-泼尼松诱导治疗后,采用伊沙佐米单药维持治疗的疗效。
Haematologica. 2018 Sep;103(9):1518-1526. doi: 10.3324/haematol.2017.185991. Epub 2018 Jun 28.
9
Global Burden of Multiple Myeloma: A Systematic Analysis for the Global Burden of Disease Study 2016.多发性骨髓瘤全球负担:2016 年全球疾病负担研究的系统分析。
JAMA Oncol. 2018 Sep 1;4(9):1221-1227. doi: 10.1001/jamaoncol.2018.2128.
10
A systematic classification of death causes in multiple myeloma.多发性骨髓瘤死亡原因的系统分类。
Blood Cancer J. 2018 Mar 8;8(3):30. doi: 10.1038/s41408-018-0068-5.

预测多发性骨髓瘤中的静脉血栓栓塞症:IMPEDE VTE 评分的建立和验证。

Predicting venous thromboembolism in multiple myeloma: development and validation of the IMPEDE VTE score.

机构信息

Division of Hematology/Oncology, Veterans Administration St. Louis Health Care System, St. Louis, Missouri.

Division of Hematology, Washington University School of Medicine Saint Louis, St. Louis, Missouri.

出版信息

Am J Hematol. 2019 Nov;94(11):1176-1184. doi: 10.1002/ajh.25603. Epub 2019 Aug 19.

DOI:10.1002/ajh.25603
PMID:31379000
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7058359/
Abstract

Venous thromboembolism (VTE) is a common cause of morbidity and mortality among patients with multiple myeloma (MM). The International Myeloma Working Group (IMWG) developed guidelines recommending primary thromboprophylaxis, in those identified at high-risk of VTE by the presence of risk factors. The National Comprehensive Cancer Network (NCCN) has adopted these guidelines; however, they lack validation. We sought to develop and validate a risk prediction score for VTE in MM and to evaluate the performance of the current IMWG/NCCN guidelines. Using 4446 patients within the Veterans Administration Central Cancer Registry, we used time-to-event analyses to develop a risk score for VTE in patients with newly diagnosed MM starting chemotherapy. We externally validated the score using the Surveillance, Epidemiology, End Results (SEER)-Medicare database (N = 4256). After identifying independent predictors of VTE, we combined the variables to develop the IMPEDE VTE score (Immunomodulatory agent; Body Mass Index ≥25 kg/m ; Pelvic, hip or femur fracture; Erythropoietin stimulating agent; Dexamethasone/Doxorubicin; Asian Ethnicity/Race; VTE history; Tunneled line/central venous catheter; Existing thromboprophylaxis). The score showed satisfactory discrimination in the derivation cohort, c-statistic = 0.66. Risk of VTE significantly increased as score increased (hazard ratio 1.20, P = <.0001). Within the external validation cohort, IMPEDE VTE had a c-statistic of 0.64. For comparison, when evaluating the performance of the IMWG/NCCN guidelines, the c-statistic was 0.55. In summary, the IMPEDE VTE score outperformed the current IMWG/NCCN guidelines and could be considered as the new standard risk stratification for VTE in MM.

摘要

静脉血栓栓塞症(VTE)是多发性骨髓瘤(MM)患者发病率和死亡率的常见原因。国际骨髓瘤工作组(IMWG)制定了指南,建议对存在 VTE 风险因素的高危患者进行初级血栓预防。国家综合癌症网络(NCCN)采用了这些指南;然而,它们缺乏验证。我们旨在开发和验证 MM 中 VTE 的风险预测评分,并评估当前 IMWG/NCCN 指南的性能。我们使用退伍军人事务部中央癌症登记处的 4446 名患者,使用生存时间分析来为新诊断为 MM 并开始化疗的患者开发 VTE 风险评分。我们使用监测、流行病学和最终结果(SEER)-医疗保险数据库(N=4256)对该评分进行外部验证。在确定 VTE 的独立预测因素后,我们将变量组合起来开发了 IMPEDE VTE 评分(免疫调节剂;体重指数≥25kg/m2;骨盆、臀部或股骨骨折;促红细胞生成素刺激剂;地塞米松/阿霉素;亚洲人种/种族;VTE 病史;隧道式导管/中心静脉导管;现有血栓预防)。该评分在推导队列中表现出令人满意的区分度,c 统计量=0.66。随着评分的增加,VTE 的风险显著增加(风险比 1.20,P<.0001)。在外部验证队列中,IMPEDE VTE 的 c 统计量为 0.64。相比之下,当评估 IMWG/NCCN 指南的性能时,c 统计量为 0.55。总之,IMPEDE VTE 评分优于当前的 IMWG/NCCN 指南,可以被视为 MM 中 VTE 的新标准风险分层。