Acute toxicity profile and treatment response of image guided hybrid brachytherapy using Venezia applicators in locally advanced cervical cancer: a single-centre experience in Pakistan.

IF 1.3 Q4 ONCOLOGY
ecancermedicalscience Pub Date : 2025-04-01 eCollection Date: 2025-01-01 DOI:10.3332/ecancer.2025.1883
Javeria Haider, Humera Mahmood, Muhammad Faheem
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Abstract

Objective: To evaluate the efficacy and acute toxicity of hybrid brachytherapy using Venezia applicators in patients with locally advanced squamous cell carcinoma of the cervix.

Methods: This prospective study involved 41 patients treated with external beam radiotherapy (EBRT) followed by brachytherapy. Patients received EBRT doses of 45-50.4 Gy with or without simultaneous integrated boost and concurrent chemotherapy. Brachytherapy was administered using Venezia applicators, delivering high-risk clinical target volume (HRCTV) doses of 80-90 Gy or >90 Gy. Treatment responses and toxicities were assessed using Response Evaluation Criteria in Solid Tumours Criteria 1.1, Common Terminology Criteria for Adverse Events Version 5.0, respectively.

Results: After five visits, 65.9% of patients achieved complete response, 29.3% partial response and 4.9% stable disease. Acute toxicities were primarily Grade 0-1, with no Grade III or IV toxicities observed. Complete responders exhibited higher rates of Grade 0 toxicities across various parameters, including urination frequency and abdominal pain. Middle-class patients showed higher response rates, although this was not statistically significant. 46.3% Human Papillomavirus positive patients converted to negative status after treatment. There was no significant correlation of response rate with disease stage, EBRT dosage or duration of treatment.

Discussion: Hybrid brachytherapy using Venezia applicators allowed for high-dose delivery to HRCTV without exceeding organ tolerance limits, resulting in effective local control (LC) and minimal acute toxicities. The study underscores the potential of hybrid brachytherapy in improving outcomes for cervical cancer patients, particularly in low-middle-income countries. Challenges included small sample size and patient follow-up limitations.

Conclusion: Hybrid brachytherapy with Venezia applicators is effective and safe for locally advanced cervical cancer, providing high LC with minimal acute toxicity.

使用威尼斯涂抹器的图像引导混合近距离治疗局部晚期宫颈癌的急性毒性概况和治疗反应:巴基斯坦的单中心经验。
目的:评价局部进展期宫颈鳞状细胞癌应用维氏涂敷器混合近距离放射治疗的疗效和急性毒性。方法:本前瞻性研究纳入41例接受外束放疗(EBRT)后加近距离放疗的患者。患者接受EBRT剂量为45-50.4 Gy,同时或不同时进行综合增强和同步化疗。使用Venezia涂抹器进行近距离放射治疗,提供80-90 Gy或bb0 -90 Gy的高风险临床靶体积(HRCTV)剂量。治疗反应和毒性分别使用实体肿瘤标准1.1和不良事件通用术语标准5.0中的反应评价标准进行评估。结果:5次就诊后,65.9%的患者完全缓解,29.3%的患者部分缓解,4.9%的患者病情稳定。急性毒性主要为0-1级,未观察到III或IV级毒性。在各种参数中,包括排尿频率和腹痛,完全缓解者表现出更高的0级毒性发生率。中产阶级患者表现出更高的应答率,尽管这在统计学上并不显著。46.3%的人乳头瘤病毒阳性患者经治疗后转为阴性。缓解率与疾病分期、EBRT剂量或治疗时间无显著相关性。讨论:使用Venezia涂抹器的混合近距离治疗允许大剂量递送到HRCTV而不超过器官耐受极限,导致有效的局部控制(LC)和最小的急性毒性。该研究强调了混合近距离放疗在改善宫颈癌患者预后方面的潜力,特别是在中低收入国家。挑战包括样本量小和患者随访限制。结论:局部晚期子宫颈癌近距离应用Venezia贴片混合治疗安全有效,LC高,急性毒性小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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