Li Puxian, Qi Aihong, Li Qiang
Altern Ther Health Med. 2025 Jul;31(4):284-288.
To examine the clinical efficacy of bevacizumab (BEV) combined with temozolomide (TMZ) as a treatment for patients with recurrent malignant gliomas.
50 patients with recurrent malignant gliomas treated at our hospital between January 2019 and January 2022 were enrolled and randomized to the control group and combine group using a random table method, with 25 cases in each group. The control group received TMZ and the combine group received BEV plus TMZ. The disease control rate (DCR), the quality-of-life score before and after treatment, and the median 6-month progression-free survival (PFS) rate as well as adverse reactions were recorded and compared.
There was a significant difference in DCR between the combine group (80%) and the control group (52%) (χ2 = 5.556, P = .018). In each of the quality-of-life scales, the scores of the combine group were significantly greater than those of the control group after treatment, and the difference was statistically significant (P < .05). In the control group, the median PFS was 16.2 weeks, and the six-month PFS was 19.8%. However, in the combine group, the median PFS was 21.9 weeks, and the six-month PFS was 43.1% (P < .05). Comparing the two groups, the rate of adverse reactions in the control group was significantly higher (44.0% vs 12.0%) (χ2 = 6.349, P = .012).
BEV plus TMZ is remarkable in the treatment of patients with recurrent malignant gliomas. The combination treatment improves the DCR and PFS of patients and their quality of life, and does not increase adverse reactions, making it a promising approach that deserves widespread promotion and clinical application.
探讨贝伐单抗(BEV)联合替莫唑胺(TMZ)治疗复发性恶性胶质瘤患者的临床疗效。
选取2019年1月至2022年1月在我院接受治疗的50例复发性恶性胶质瘤患者,采用随机数字表法将其随机分为对照组和联合组,每组25例。对照组接受TMZ治疗,联合组接受BEV联合TMZ治疗。记录并比较两组的疾病控制率(DCR)、治疗前后的生活质量评分、6个月无进展生存期(PFS)中位数以及不良反应。
联合组(80%)与对照组(52%)的DCR差异有统计学意义(χ2 = 5.556,P = .018)。在各个生活质量量表中,联合组治疗后的得分均显著高于对照组,差异有统计学意义(P < .05)。对照组的PFS中位数为16.2周,6个月PFS率为19.8%。而联合组的PFS中位数为21.9周,6个月PFS率为43.1%(P < .05)。两组比较,对照组的不良反应发生率显著更高(44.0% 对12.0%)(χ2 = 6.349,P = .012)。
BEV联合TMZ治疗复发性恶性胶质瘤患者效果显著。联合治疗提高了患者的DCR和PFS以及生活质量,且未增加不良反应,是一种值得广泛推广和临床应用的有前景的治疗方法。