转移性结直肠癌患者瑞非尼疗效与给药剂量强度/体表面积的关系研究

K. Eser, E. Sezer, V. Erçolak, A. Inal, A. Ata, Hakan Basir, M. Berkeşoğlu
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引用次数: 0

摘要

研究了相对剂量强度(RDI)在不同类型实体癌治疗中的意义。然而,RDI可能不能准确反映瑞非尼的治疗强度,因为大多数患者不能耐受标准剂量。我们旨在通过比较2M-DBR、2个月RDI与治疗反应的关系,探讨2个月时递送剂量强度/体表面积(BSA)比(2M-DBR)的疗效。材料与方法:对2015年至2020年53例患者的瑞非尼治疗反应进行回顾性研究。在治疗开始后8-12周进行计算机断层扫描。我们还研究了与高2M-DBR和BSA相关的临床因素。结果:高2M-DBR组的客观有效率显著高于低2M-DBR组(p<0.064)。高2M-DBR患者的总生存期(p=0.445)和无进展生存期(p=0.524)均长于低2M-DBR患者,但差异无统计学意义。高BSA患者(22%)对160 mg瑞非尼的耐受性优于低BSA患者(0%)(p=0.011)。结论:牛血清白蛋白是决定瑞非尼耐受剂量的关键因素。2M-DBR在反映治疗强度方面起着关键作用,是预测mCRC对瑞非尼反应的有用工具。
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Investigation of Regorafenib Efficacy in Patients with Metastatic Colorectal Carcinoma in Relation to the Delivered Dose Intensity/Body Surface Area
The significance of relative dose intensity (RDI) in the treatment of various types of solid cancers has been studied. Nevertheless, RDI may not accurately reflect the treatment intensity of regorafenib, where the standard dose cannot be tolerated by most patients. We aimed to investigate the efficacy of the delivered dose intensity/body surface area (BSA) ratio at 2 months (2M-DBR) by comparing the relationship between 2M-DBR, RDI at 2 months, and the therapeutic response. Material and Methods: The thera- peutic response to regorafenib was studied in 53 patients retrospectively from 2015 to 2020. Computed tomography scans were performed at 8-12 weeks after the initiation of treatment. We also investigated the clinical factors associated with high 2M-DBR and BSA. Results: Pa- tients with high 2M-DBR achieved significantly better objective response rates than those with low 2M-DBR (p<0.064). Patients with high 2M-DBR experienced longer overall survival (p=0.445) and progression-free survival (p=0.524) than those with low 2M-DBR but the dif- ference was not statistically significant. Tolerance to 160 mg regorafenib was found to be better in patients with high BSA (22%) than in a patient with low BSA (0%) (p=0.011). Conclusion: BSA is crucial in determining the tolerance dose of regorafenib. 2M-DBR plays a key role in reflecting treatment intensity and is a useful tool for predicting the response to regorafenib in mCRC.
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审稿时长
29 weeks
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