Department of Nursing, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Department of Management Information Systems, National Chung Cheng University Chiayi, Chiayi, Taiwan.
Kaohsiung J Med Sci. 2024 Jun;40(6):589-598. doi: 10.1002/kjm2.12838. Epub 2024 May 2.
In 2008, sorafenib became the first approved systemic therapeutic agent for advanced HCC. Although its pharmacological efficacy has been established, reimbursement for such a new, high-cost drug, as well as physicians' awareness and prescription practice, likewise contribute to its clinical effectiveness. We therefore conducted a retrospective study using 38 sorafenib-eligible, advanced HCC patients when sorafenib was approved but not yet reimbursed as a control and 216 patients during the reimbursed era. Study group showed longer survival at 8.2 months versus the control's 4.9 months (p = 0.0063 hazard ratio: 0.612 [0.431 ~ 0.868], p = 0.0059). Among the 42 (19.4%) patients who survived more than 2 years, 50% had tumor rupture, and all 32 patients with portal vein tumor thrombus and/or extrahepatic metastasis received sorafenib (p = 0.003). Furthermore, during their first 2 years of HCC management, sorafenib had been given in 29.1% of the treatment courses among survivors between 2 and 5 years while it was prescribed in 55.8% among the more than 5 years survivor group (p < 0.001). In conclusion, survival of sorafenib-eligible HCC patients significantly improved after reimbursement. Patients who underwent longer sorafenib treatment had a survival advantage, except for those with tumor rupture. Reimbursement and awareness of prescriptions for a newly introduced medication therefore improve clinical effectiveness.
2008 年,索拉非尼成为首个被批准用于晚期 HCC 的系统治疗药物。虽然其药理学疗效已经确定,但这种新的、高成本药物的报销以及医生的认识和处方实践同样有助于其临床疗效。因此,我们进行了一项回顾性研究,使用了索拉非尼获批但尚未报销的 38 名晚期 HCC 患者作为对照(研究组),以及在报销时代的 216 名患者作为对照组。研究组的中位生存期为 8.2 个月,而对照组为 4.9 个月(p=0.0063 风险比:0.612 [0.431~0.868],p=0.0059)。在 42 名(19.4%)存活超过 2 年的患者中,有 50%的患者肿瘤破裂,所有 32 名门静脉癌栓和/或肝外转移的患者都接受了索拉非尼治疗(p=0.003)。此外,在 HCC 管理的前 2 年中,在 2 至 5 年存活期的患者中,有 29.1%的治疗疗程中使用了索拉非尼,而在超过 5 年存活期的患者中,有 55.8%的患者使用了索拉非尼(p<0.001)。总之,索拉非尼适用的 HCC 患者的生存率在报销后显著提高。接受更长时间索拉非尼治疗的患者具有生存优势,除了肿瘤破裂的患者。因此,新引入药物的报销和处方意识可以提高临床疗效。