1 Thomas Jefferson University, Philadelphia, Pennsylvania.
2 University of Texas Austin and Baylor Scott & White Health, Temple, Texas.
J Manag Care Spec Pharm. 2018 Jan;24(1):39-46. doi: 10.18553/jmcp.2018.24.1.39.
With the continuous rise in costs for oncology drugs, the American Society of Clinical Oncology (ASCO), the Institute for Clinical and Economic Review (ICER), the Memorial Sloan Kettering Cancer Center's Drug Abacus (DrugAbacus), and the National Comprehensive Cancer Network (NCCN) have developed value-based frameworks (VBFs) to assist stakeholders in formulary and treatment decision-making processes. Since emerging VBFs have the potential to affect available treatment options for patients, it is important to understand the differences associated with these VBFs within various therapeutic areas.
To (a) compare VBFs across 3 therapeutic options for relapsed or refractory multiple myeloma (RRMM) and (b) identify challenges and limitations associated with real-world decision making using VBFs in the U.S. marketplace.
The values of regimens carfilzomib (CFZ), elotuzumab (ELO), and ixazomib (IX) were generated using the ASCO, NCCN, ICER, and DrugAbacus VBFs. These regimens, used for second- or third-line treatment of RRMM, shared a common comparator in clinical trials: lenalidomide + dexamethasone (LEN + DEX). ASCO's 2016 VBF, which incorporated clinical benefit, toxicity, and bonus points, was used to generate a net health benefit score, along with the drug wholesale acquisition cost, for each regimen compared with LEN + DEX. Results of the 2016 NCCN Evidence Blocks for multiple myeloma and the ICER 2016 report of treatment options for RRMM were extracted to generate the value of CFZ, ELO, and IX. No output was generated from DrugAbacus because of the lack of regimens included in the test case. Shortcomings associated with running the test case in RRMM for each VBF were also identified.
Among the 3 therapeutic agents, CFZ, in combination with LEN + DEX, was the most valued. ASCO and ICER VBFs suggested that CFZ + LEN + DEX may be the most valued, followed by ELO + LEN + DEX and IX + LEN + DEX. NCCN suggested that LEN + DEX may be the most valued followed by CFZ + LEN + DEX, IX + LEN + DEX, and ELO + LEN + DEX. A number of shortcomings were noted across each VBF, such as complexities of drug evidence evaluation with the ASCO VBF, the inability to adjust the ICER and NCCN VBFs to specific populations, and subjectivity associated with the NCCN VBF and DrugAbacus.
Although the test case provided some consensus on treatment decisions, there is much nuance and limitations with the VBFs available for RRMM. Clearer objectivity and better adaptability to specific treatment decisions are warranted.
No outside funding supported this study. The authors have nothing to disclose. All authors contributed to study concept and design, as well data collection and interpretation. Djatche and Goble wrote and revised the manuscript, along with Chun and Varga. Portions of this work have previously been presented at the AMCP Managed Care and Specialty Pharmacy Annual Meeting 2017 in Denver, Colorado, March 27-30, 2017, and at the ISPOR 22nd Annual International Meeting in Boston, Massachusetts, May 20-24, 2017.
随着肿瘤药物成本的不断上升,美国临床肿瘤学会(ASCO)、临床与经济评论研究所(ICER)、纪念斯隆凯特琳癌症中心药物算盘(DrugAbacus)和国家综合癌症网络(NCCN)已经开发了基于价值的框架(VBFs),以帮助利益相关者在处方和治疗决策过程中。由于新兴的 VBF 有可能影响患者的可用治疗选择,因此了解这些 VBF 在不同治疗领域中的差异非常重要。
(a)比较 3 种复发性或难治性多发性骨髓瘤(RRMM)治疗方案的 VBF,并(b)确定在美国市场使用 VBF 进行实际决策所面临的挑战和局限性。
使用 ASCO、NCCN、ICER 和 DrugAbacus VBF 生成卡非佐米(CFZ)、依鲁单抗(ELO)和伊沙佐米(IX)方案的价值。这些方案用于 RRMM 的二线或三线治疗,在临床试验中与来那度胺+地塞米松(LEN+DEX)有共同的比较剂。ASCO 2016 年的 VBF 纳入了临床获益、毒性和附加分,用于生成每个方案与 LEN+DEX 相比的净健康获益评分和药物批发采购成本。提取了 2016 年 NCCN 多发性骨髓瘤证据块和 ICER 2016 年 RRMM 治疗方案报告的结果,以生成 CFZ、ELO 和 IX 的价值。由于测试案例中未包含方案,因此 DrugAbacus 没有生成任何结果。还确定了每个 VBF 在 RRMM 中运行测试案例的缺点。
在 3 种治疗药物中,CFZ 联合 LEN+DEX 的价值最高。ASCO 和 ICER VBF 表明 CFZ+LEN+DEX 可能最有价值,其次是 ELO+LEN+DEX 和 IX+LEN+DEX。NCCN 表明 LEN+DEX 可能最有价值,其次是 CFZ+LEN+DEX、IX+LEN+DEX 和 ELO+LEN+DEX。每个 VBF 都存在许多缺点,例如 ASCO VBF 中药物证据评估的复杂性、无法根据特定人群调整 ICER 和 NCCN VBF 以及 NCCN VBF 和 DrugAbacus 的主观性。
尽管测试案例在治疗决策方面提供了一些共识,但 RRMM 可用的 VBF 存在很多细微差别和局限性。需要更明确的客观性和更好地适应特定的治疗决策。
本研究没有外部资金支持。作者没有任何关联。所有作者都参与了研究概念和设计、数据收集和解释。Djatche 和 Goble 撰写并修改了手稿,Chun 和 Varga 也参与了这一过程。这项工作的一部分此前曾在 2017 年 3 月 27 日至 30 日在科罗拉多州丹佛市举行的 AMCP 管理式医疗和专科药房年会 2017 年和 2017 年 5 月 20 日至 24 日在马萨诸塞州波士顿举行的 ISPOR 第 22 届年会上展示过。