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本文引用的文献

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Lenalidomide Maintenance Compared With Placebo in Responding Elderly Patients With Diffuse Large B-Cell Lymphoma Treated With First-Line Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone.来那度胺维持治疗对比安慰剂用于一线利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松治疗的老年弥漫性大 B 细胞淋巴瘤患者。
J Clin Oncol. 2017 Aug 1;35(22):2473-2481. doi: 10.1200/JCO.2017.72.6984. Epub 2017 Apr 20.
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2016 US lymphoid malignancy statistics by World Health Organization subtypes.2016年按世界卫生组织亚型分类的美国淋巴系统恶性肿瘤统计数据。
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Randomized Phase 2 Open-Label Study of R-CHOP ± Bortezomib in Patients (Pts) With Untreated Non-Germinal Center B-Cell-like (Non-GCB) Subtype Diffuse Large Cell Lymphoma (DLBCL): Results From the Pyramid Trial (NCT00931918).R-CHOP方案±硼替佐米用于未经治疗的非生发中心B细胞样(Non-GCB)亚型弥漫性大B细胞淋巴瘤(DLBCL)患者的随机2期开放标签研究:金字塔试验(NCT00931918)结果
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Prognostic Significance of Diffuse Large B-Cell Lymphoma Cell of Origin Determined by Digital Gene Expression in Formalin-Fixed Paraffin-Embedded Tissue Biopsies.通过数字基因表达确定福尔马林固定石蜡包埋组织活检中弥漫性大B细胞淋巴瘤细胞起源的预后意义
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Use and Costs for Tumor Gene Expression Profiling Panels in the Management of Breast Cancer From 2006 to 2012: Implications for Genomic Test Adoption Among Private Payers.2006年至2012年肿瘤基因表达谱检测在乳腺癌管理中的应用与成本:对私人付费者采用基因组检测的影响
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Updating cost-effectiveness--the curious resilience of the $50,000-per-QALY threshold.更新成本效益——每质量调整生命年5万美元阈值令人好奇的韧性。
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9
Lenalidomide combined with R-CHOP overcomes negative prognostic impact of non-germinal center B-cell phenotype in newly diagnosed diffuse large B-Cell lymphoma: a phase II study.来那度胺联合 R-CHOP 克服了新诊断弥漫性大 B 细胞淋巴瘤中非生发中心 B 细胞表型的不良预后影响:一项 II 期研究。
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探索弥漫性大B细胞淋巴瘤精准医学治疗策略的潜在成本效益。

Exploring the potential cost-effectiveness of precision medicine treatment strategies for diffuse large B-cell lymphoma.

作者信息

Chen Qiushi, Staton Ashley D, Ayer Turgay, Goldstein Daniel A, Koff Jean L, Flowers Christopher R

机构信息

a Massachusetts General Hospital Institute for Technology Assessment , Boston , MA , USA.

b Harvard Medical School , Boston , MA , USA.

出版信息

Leuk Lymphoma. 2018 Jul;59(7):1700-1709. doi: 10.1080/10428194.2017.1390230. Epub 2017 Oct 25.

DOI:10.1080/10428194.2017.1390230
PMID:29065744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5918224/
Abstract

Activated B-cell-like (ABC) diffuse large B-cell lymphoma (DLBCL) is associated with worse survival after standard rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (RCHOP) chemoimmunotherapy compared to germinal center B-cell-like (GCB) subtype. Preliminary evidence suggests that benefits from novel agents may vary by subtype. Hypothesizing that treatment stratified by DLBCL subtype could be potentially cost-effective, we developed micro-simulation models to compare three first-line treatment strategies: (1) standard RCHOP for all patients (2) subtype testing followed by RCHOP for GCB and novel treatment for ABC DLBCL, and (3) novel treatment for all patients. Based on phase 2 evidence, we used lenalidomide + RCHOP as a surrogate novel treatment. The subtype-based approach showed a favorable incremental cost-effectiveness ratio of $15,015/quality-adjusted life year compared with RCHOP. Although our exploratory analyses demonstrated a wide range of conditions where subtype-based treatment remained cost-effective, data from phase 3 trials are needed to validate our models' findings and draw definitive conclusions.

摘要

与生发中心B细胞样(GCB)亚型相比,活化B细胞样(ABC)弥漫性大B细胞淋巴瘤(DLBCL)在接受标准利妥昔单抗、环磷酰胺、阿霉素、长春新碱和泼尼松(RCHOP)化疗免疫治疗后的生存率更低。初步证据表明,新型药物的疗效可能因亚型而异。假设根据DLBCL亚型进行分层治疗可能具有潜在的成本效益,我们开发了微观模拟模型,以比较三种一线治疗策略:(1)所有患者均采用标准RCHOP治疗;(2)先进行亚型检测,GCB患者采用RCHOP治疗,ABC DLBCL患者采用新型治疗;(3)所有患者均采用新型治疗。基于2期证据,我们使用来那度胺+RCHOP作为替代新型治疗方法。与RCHOP相比,基于亚型的治疗方法显示出良好的增量成本效益比,为15,015美元/质量调整生命年。尽管我们的探索性分析表明,在多种情况下基于亚型的治疗仍具有成本效益,但仍需要3期试验的数据来验证我们模型的结果并得出明确结论。