Grossi Fernanda Santos, Balbinotti Rodrigo Rossi, Muller Gabriel Cardozo, Chagas Luciana Borges, Tregnago Aline Caldart, Kliemann Lucia Maria, Magno Valentino Antônio, Binda Marcia Luiza Montalvao Appel, Vettorazzi Janete
Postgraduate Program in Health Sciences: Gynecology and Obstetrics, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, 90610-264, Brazil.
Nucleus of Studies and Research in Sexuality of Rio Grande do Sul (NEPESEX), CNPq, Porto Alegre, Rio Grande do Sul, Brazil.
J Sex Med. 2025 Jun 3;22(6):1043-1052. doi: 10.1093/jsxmed/qdaf083.
Radiotherapy for cervical cancer can lead to genitourinary syndrome (GUS), which negatively impacts sexual function and the quality of life among female cancer survivors.
To evaluate the efficacy of promestriene and non-ablative radiofrequency (NARF) in treating GUS and its effects on sexual function in women who have undergone radiotherapy for cervical cancer (CC).
In this pilot randomized clinical trial included 24 women who had received radiotherapy and/or brachytherapy for CC within the past five years. Participants were randomized to receive treatment with promestriene cream or intravaginal (NARF). Sexual function was assessed pre- and post-treatment using the Female Sexual Function Index (FSFI). Vaginal symptoms were evaluated using a visual analog scale (VAS), and histological analyses of vaginal biopsies were performed before and after the intervention.
The main outcomes measured were improvements in sexual function and reductions in vaginal symptoms.
Significant improvements in FSFI scores and reductions in vaginal symptom intensity were observed in both treatment groups. The median FSFI score increased from 13.0 to 23.1 after treatment. Histological analysis demonstrated a significant increase in epithelial thickness and an improvement in stromal quality in both groups. No significant differences were noted between the promestriene and (NARF) groups concerning sexual function improvements or symptom reduction.
Both promestriene and (NARF) proved effective and safe enhancing sexual function and reducing vaginal symptoms in post-radiotherapy CC survivors.
The study's strengths include its randomized design and comprehensive assessment of subjective and objective outcomes. However, the small sample size and limited follow-up period limit the generalization and long-term applicability of the findings.
Both promestriene and (NARF) significantly improve sexual function and alleviate vaginal symptoms in women treated with radiotherapy for CC, presenting viable options for managing GUS in this patient population.
宫颈癌放疗可导致泌尿生殖综合征(GUS),对女性癌症幸存者的性功能和生活质量产生负面影响。
评估普罗雌烯和非消融性射频(NARF)治疗GUS的疗效及其对接受宫颈癌(CC)放疗女性性功能的影响。
在这项前瞻性随机临床试验中,纳入了24名在过去五年内接受过CC放疗和/或近距离放疗的女性。参与者被随机分为接受普罗雌烯乳膏或阴道内(NARF)治疗。治疗前后使用女性性功能指数(FSFI)评估性功能。使用视觉模拟量表(VAS)评估阴道症状,并在干预前后对阴道活检进行组织学分析。
主要测量结果为性功能改善和阴道症状减轻。
两个治疗组的FSFI评分均有显著改善,阴道症状强度降低。治疗后FSFI评分中位数从13.0提高到23.1。组织学分析表明,两组上皮厚度均显著增加,基质质量有所改善。普罗雌烯组和(NARF)组在性功能改善或症状减轻方面未观察到显著差异。
普罗雌烯和(NARF)均被证明对放疗后CC幸存者增强性功能和减轻阴道症状有效且安全。
该研究的优点包括其随机设计以及对主观和客观结果的综合评估。然而,样本量小和随访期有限限制了研究结果的推广和长期适用性。
普罗雌烯和(NARF)均能显著改善接受CC放疗女性的性功能并减轻阴道症状,为该患者群体管理GUS提供了可行的选择。