Pharmacy Unit, Hospital Joan XXIII, Tarragona, Spain.
Farm Hosp. 2024 Sep-Oct;48(5):222-229. doi: 10.1016/j.farma.2024.03.008. Epub 2024 Apr 27.
The first targeted therapy in oncology, imatinib, revolutionized chronic myeloid leukemia (CML) treatment and spurred research in targeted therapies for various cancers. CML results from a chromosomal translocation, forming the BCR-ABL1 fusion gene. Asciminib has been recently approved for third-line refractory or intolerant patients. Treatment-free remission (TFR) is attainable with sustained deep molecular response (DMR) and this approach could be incorporated into pharmacoeconomic models.
To establish a cost-effectiveness model comparing asciminib to approved third-generation tyrosine kinase inhibitors (TKIs) (bosutinib and ponatinib) with a focus on achieving TFR. Additionally, the budgetary impact of incorporating asciminib as a therapeutic alternative is assessed.
This model is based on a Markov chain with 7 states. The condition for achieving TFR is to remain for 5 years in DMR state. Efficacy of the model was measured in QALYs, and the costs included in the base case analysis are based in Spain. A probabilistic (PSA) and deterministic analysis (DSA) were carried out to assess the variability of the model. There were achieved 2 independent models comparing asciminib vs bosutinib and asciminib vs ponatinib.
Asciminib, when compared with ponatinib, is a cost-saving alternative, as efficacy is similar between alternatives, and asciminib have a lower cost of 30,275€. Asciminib showed 4.33 more QALYs and a higher cost (203,591€) than bosutinib, resulting in an ICER of €47,010.49 per QALY. PSA shows that the parameters with higher influence in the variability of the model were the probability of transitioning to BP and probabilities of achieving MMR and DMR. A one-way analysis reports that the drug cost has a higher influence on both models, and the discount rate significantly affects the asciminib vs bosutinib model.
Asciminib broadens therapeutic choices for patient's refractory or intolerant to 2 prior lines of treatment in a cost-effectiveness manner. The costs of drugs significantly impact the overall cost of the disease, emphasizing the importance of the selected discount rates for each drug. Given the relatively low incidence of CML, the introduction of asciminib has a limited budgetary impact, warranting individualized decisions based on patient`s clinical characteristics.
肿瘤学中的第一种靶向治疗药物伊马替尼彻底改变了慢性髓性白血病(CML)的治疗方法,并推动了针对各种癌症的靶向治疗研究。CML 是由染色体易位形成 BCR-ABL1 融合基因引起的。阿西替尼最近已被批准用于三线治疗耐药或不耐受的患者。通过持续的深度分子反应(DMR)可以实现无治疗缓解(TFR),这种方法可以纳入药物经济学模型。
建立一种成本效益模型,比较阿西替尼与已批准的第三代酪氨酸激酶抑制剂(TKIs)(博舒替尼和帕纳替尼),重点是实现 TFR。此外,还评估了将阿西替尼纳入治疗选择的预算影响。
该模型基于一个具有 7 个状态的马尔可夫链。达到 TFR 的条件是在 DMR 状态下持续 5 年。模型的疗效以 QALYs 衡量,基础病例分析中包含的成本基于西班牙。进行了概率(PSA)和确定性分析(DSA),以评估模型的可变性。已经建立了两个独立的模型,比较阿西替尼与博舒替尼和阿西替尼与帕纳替尼。
与帕纳替尼相比,阿西替尼是一种节省成本的选择,因为替代方案的疗效相似,而阿西替尼的成本较低,为 30275 欧元。阿西替尼比博舒替尼有 4.33 个更多的 QALYs 和更高的成本(203591 欧元),导致每 QALY 的 ICER 为 47010.49 欧元。PSA 显示,对模型变异性影响较大的参数是向 BP 转移的概率和达到 MMR 和 DMR 的概率。单向分析报告称,药物成本对两个模型的影响都较大,折扣率对阿西替尼与博舒替尼模型的影响显著。
阿西替尼以具有成本效益的方式拓宽了对二线治疗耐药或不耐受的患者的治疗选择。药物成本对疾病的总体成本有重大影响,强调了为每种药物选择折扣率的重要性。鉴于 CML 的相对低发病率,阿西替尼的引入对预算的影响有限,需要根据患者的临床特征做出个体化决策。