Tsai Hsiang-Lin, Shi Hon-Yi, Chen Yen-Cheng, Huang Ching-Wen, Su Wei-Chih, Chang Tsung-Kun, Li Ching-Chun, Chen Po-Jung, Yeh Yung-Sung, Yin Tzu-Chieh, Wang Jaw-Yuan
Division of Colorectal Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung 80708, Taiwan.
Department of Surgery, Faculty of Medicine, College of Medicine, Kaohsiung Medical University Kaohsiung 80708, Taiwan.
Am J Cancer Res. 2023 Sep 15;13(9):4039-4056. eCollection 2023.
This study investigated the cost-effectiveness and quality of life (QoL) within 1 year of receiving mFOLOFX6 with or without a targeted drug (bevacizumab or ramucirumab) as second-line treatment among patients with metastatic colorectal cancer (mCRC) following the failure of FOLFIRI + bevacizumab as first-line treatment. This prospective cohort study included patients who received a diagnosis of mCRC between March 2015 and May 2020. QoL was evaluated before treatment and at 6 months and 1 year posttreatment. All related variables were controlled using the inverse probability of treatment weighting method. Generalized estimating equations with the difference-in-difference method was used to explore changes in QoL. The incremental cost-utility ratio (ICUR) of the two groups was simulated using the annual-cycle Markov decision tree model. Finally, 39 and 76 patients were included in the targeted and nontargeted agent groups, respectively. At 6 months after treatment, QoL of the two groups improved significantly, but the targeted agent group had significantly better QoL than did the nontargeted agent group at 1 year posttreatment (P < 0.05). When the time frame was set to 20 years, the ICUR of the targeted agent group compared with the nontargeted agent group was US$32,052 per quality-adjusted life years. Addition of a targeted drug to the second-line mFOLOFX6 regimen not only improved the patients' QoL but was also more cost effective when the willingness-to-pay threshold was set at US$33,004 (the per capita gross domestic product of Taiwan). These patients should be reimbursed for these targeted agents by the National Health Insurance scheme in Taiwan.
本研究调查了在一线治疗FOLFIRI + 贝伐单抗失败后,接受mFOLOFX6联合或不联合靶向药物(贝伐单抗或雷莫西尤单抗)作为二线治疗的转移性结直肠癌(mCRC)患者1年内的成本效益和生活质量(QoL)。这项前瞻性队列研究纳入了2015年3月至2020年5月期间被诊断为mCRC的患者。在治疗前、治疗后6个月和1年评估QoL。所有相关变量均使用治疗权重的逆概率方法进行控制。采用具有差异 - 差异法的广义估计方程来探索QoL的变化。使用年度循环马尔可夫决策树模型模拟两组的增量成本 - 效用比(ICUR)。最后,靶向药物组和非靶向药物组分别纳入了39例和76例患者。治疗后6个月,两组的QoL均显著改善,但治疗后1年,靶向药物组的QoL显著优于非靶向药物组(P < 0.05)。当时间范围设定为20年时,靶向药物组与非靶向药物组相比的ICUR为每质量调整生命年32,052美元。在二线mFOLOFX6方案中添加靶向药物不仅改善了患者的QoL,而且当支付意愿阈值设定为33,004美元(台湾地区人均国内生产总值)时,成本效益更高。台湾地区的国民健康保险计划应为这些患者报销这些靶向药物。