国际肿瘤学杂志 ›› 2026, Vol. 53 ›› Issue (4): 219-223.doi: 10.3760/cma.j.cn371439-20250520-00036

• 论著 • 上一篇    下一篇

同步放化疗后安罗替尼维持治疗局部晚期宫颈癌的短期疗效与临床观察

韩宇飞1, 李凤梅2, 张维娜1, 张萍1, 侯萍1()   

  1. 1 青岛市市立医院妇科青岛 266011
    2 青岛市市立医院口腔科青岛 266011
  • 收稿日期:2025-05-20 出版日期:2026-04-08 发布日期:2026-04-01
  • 通讯作者: 侯萍,Email: 13708950098@139.com
  • 基金资助:
    山东省医学会临床科研基金-齐鲁专项(YXH2022ZX02155)

Short-term efficacy and clinical outcomes of concurrent chemoradiotherapy followed by anlotinib maintenance treatment in patients with locally advanced cervical cancer

Han Yufei1, Li Fengmei2, Zhang Weina1, Zhang Ping1, Hou Ping1()   

  1. 1 Department of GynecologyQingdao Municipal HospitalQingdao 266011, China
    2 Department of StomatologyQingdao Municipal HospitalQingdao 266011, China
  • Received:2025-05-20 Online:2026-04-08 Published:2026-04-01
  • Contact: Hou Ping, Email: 13708950098@139.com
  • Supported by:
    Clinical Scientific Research Fund of Shandong Medical Association-Qilu Special Project(YXH2022ZX02155)

摘要:

目的 观察安罗替尼维持治疗同步放化疗后局部晚期宫颈癌(LACC)患者的疗效及安全性。方法 选取2021年10月至2022年8月青岛市市立医院68例LACC患者为研究对象,根据治疗方案不同分为观察组32例(接受同步放化疗后继续安罗替尼维持治疗),对照组36例(接受同步放化疗),21 d为1个疗程。每个疗程结束后复查血清肿瘤标志物鳞状细胞癌抗原(SCC),每2个疗程给予影像学MR评估宫颈病灶大小变化,观察两组患者药物相关不良反应发生情况。比较两组患者的无进展生存期(PFS)。结果 至随访结束,观察组的SCC为(5.81±0.62)ng/ml,对照组的SCC为(6.79±0.53)ng/ml;观察组的宫颈病灶最大径为(3.66±0.84)cm,对照组的宫颈病灶最大径为(4.32±0.68)cm,差异均有统计学意义(t=8.50,P<0.001;t=4.32,P<0.001)。观察组的完全缓解率为81.25%(26/32),明显高于对照组的50.00%(18/36),差异有统计学意义(χ2=7.24,P=0.007)。观察组患者的继发性高血压发生率为46.88%(15/32),高于对照组的22.22%(8/36),差异有统计学意义(χ2=4.60,P=0.032),均为1~2级;观察组与对照组的血液毒性反应[62.50%(20/32)比50.00%(18/36)]、胃肠道反应[34.38%(11/32)比25.00%(9/36)]、放射性膀胱炎[15.63%(5/32)比11.11%(4/36)]、放射性直肠炎[18.75%(6/32)比11.11%(4/36)]、蛋白尿[21.88%(7/32)比19.44%(7/36)]发生率比较,差异均无统计学意义(χ2=1.07,P=0.300;χ2=0.72,P=0.397;χ2=0.30,P=0.584;χ2=0.79,P=0.375;χ2=0.06,P=0.805)。观察组患者的中位PFS为23.75个月,明显长于对照组患者的15.16个月,差异有统计学意义(χ2=4.28,P=0.034)。结论 同步放化疗后安罗替尼维持治疗LACC较仅同步放化疗的完全缓解率高,不良反应可控,可延长患者的PFS。

关键词: 宫颈肿瘤, 化放疗, 药物相关性副作用和不良反应, 预后, 安罗替尼

Abstract:

Objective To observe the efficacy and safety of anlotinib maintenance treatment in patients with locally advanced cervical cancer (LACC) after concurrent chemoradiotherapy. Methods From October 2021 to August 2022, 68 patients with LACC admitted to Qingdao Municipal Hospital were selected as the research subjects. According to different treatment regimens, they were divided into an observation group of 32 cases (receiving anlotinib maintenance treatment after concurrent chemoradiotherapy) and a control group of 36 cases (receiving concurrent chemoradiotherapy alone), with 21 days as one course of treatment. Serum tumor marker squamous cell carcinoma antigen (SCC) was reexamined after each course of treatment. Imaging MR was performed every 2 courses of treatment to evaluate the changes in the size of cervical lesions, and the occurrence of drug-related adverse reactions in the two groups of patients was observed. The progression-free survival (PFS) was compared between the two groups. Results By the end of follow-up,the SCC and maximum cervical lesion diameter in the observation group were (5.81±0.62) ng/ml and (3.66±0.84) cm, respectively, and those in the control group were (6.79±0.53) ng/ml and (4.32±0.68) cm, respectively, with statistically significant differences (t=8.50, P<0.001; t=4.32, P<0.001). The complete remission rate of the observation group was 81.25% (26/32), which was significantly higher than that of the control group (50.00%, 18/36), with a statistically significant difference (χ2=7.24, P=0.007). The incidence of secondary hypertension in the observation group was 46.88% (15/32), higher than 22.22% (8/36) in the control group, with a statistically significant difference (χ2=4.60, P=0.032), however, all were grade 1-2. There were no statistically significant differences in the incidence of hematological toxicity [62.50% (20/32) vs. 50.00% (18/36), χ2=1.07, P=0.300], gastrointestinal reactions [34.38% (11/32) vs. 25.00% (9/36), χ2=0.72, P=0.397], radiation cystitis [15.63% (5/32) vs. 11.11% (4/36), χ2=0.30, P=0.584], radiation proctitis [18.75% (6/32) vs. 11.11% (4/36), χ2=0.79, P=0.375] and proteinuria [21.88% (7/32) vs. 19.44% (7/36), χ2=0.06, P=0.805] between the observation group and the control group. The median PFS in the observation group was 23.75 months, which was significantly longer than 15.16 months of the control group, with a statistically significant difference (χ2=4.28, P=0.034). Conclusions The complete remission rate of concurrent chemoradiotherapy followed by anlotinib maintenance treatment for LACC is higher than that of concurrent chemoradiotherapy alone, the adverse reactions are controllable, and can prolong the PFS of patients.

Key words: Uterine cervical neoplasms, Chemoradiotherapy, Drug-related side effects and adverse reactions, Prognosis, Anlotinib