Henri-Mondor Breast Center, hôpitaux universitaires Henri-Mondor, 51, avenue Marechal de Lattre de Tassigny, 94010 Créteil, France; Department of Maxillofacial Surgery, Plastic and Reconstructive, hôpitaux universitaires Henri-Mondor, 51, avenue Marechal de Lattre de Tassigny, 94010 Créteil, France; University of Paris East Creteil (UPEC), Créteil, France.
Henri-Mondor Breast Center, hôpitaux universitaires Henri-Mondor, 51, avenue Marechal de Lattre de Tassigny, 94010 Créteil, France; Gynecological Surgery Department, Bégin Army Teaching Hospital, 69, avenue de Paris, 94160 Saint-Mandé, France.
Ann Chir Plast Esthet. 2020 Jul;65(4):e23-e31. doi: 10.1016/j.anplas.2020.05.002. Epub 2020 Jun 5.
Quality of life preservation after anti-cancer therapy is a major challenge for breast cancer survivors. Approximately 42-70% of patients who receive systemic therapy for breast cancer, including endocrine therapy, will develop vulvovaginal atrophy (VVA). For these patients, the commonly proposed gel-based treatments for topical applications are restrictive. Recently, innovative, non-hormonal therapeutic approaches, such as laser therapy, have emerged. The purpose of this feasibility study is to investigate the safety and efficacy of CO laser therapy in women with a history of breast cancer.
This prospective monocentric study included 20 patients with vulvovaginal atrophy who were treated at Henri Mondor University Hospital between 2017 and 2018. We included patients with a vaginal health index (VHI) score<15 and a contraindication for hormone administration due to a history of breast cancer. Two carbon dioxide laser sessions were used. The treatment was delivered using the following settings: vaginal tightening, FinePulse (pulse width 0.9ms), and energy density of 11.5J/cm that allows coverage of 70% of the targeted vaginal area to be treated. All patients had their follow-up visit at one (M1), three (M3), and six (M6) months after the first treatment to evaluate efficacy of the treatment on vulvovaginal atrophy. Vaginal health index score and female sexual distress (FSD) score were used to assess treatment efficacy and its impact on sexual quality of life. A score≥11 was associated with sexual dysfunction. The vaginal health index and female sexual distress scores were evaluated at baseline, M1, M3, and M6 of follow-up.
The mean age of the patients was 56.1±8.8 years (range, 27-69 years). Seventeen of the 20 patients had experienced menopause (mean menopausal age, 51.25±1.5 years). At inclusion, the mean vaginal health index and the female sexual distress scores were 10.58±1.71 and 21.36±15.10, respectively. Fourteen out of 20 patients (70%) had FSD scores≥11 at the baseline. At M1, the mean vaginal health index score increased significantly to 13.42±2.3 (P=0.03), which represented an improvement of 21% from the baseline. A persistent and significant improvement in the vaginal health index score was observed at M6, with the score increasing to 16.75±4.23 post-treatment (P<0.0001), representing a 34% improvement from the mean baseline score. The mean female sexual distress at M1 was 19.83±13.57, representing a 7% decrease compared to the baseline scores (P<0.01). At M3, the female sexual distress significantly decreased to 13.88±15.58, representing an improvement of 35% (P=0.006). It increased to 10.35±14.7 at M6, representing an improvement of 52% (P=0.001). At M3, 35% of the patients had a female sexual distress score>11, and at M6, only 15% had a female sexual distress score>11. No side effects were reported during follow-up.
This pilot feasibility study showed that carbon dioxide laser treatment appears to be an effective and safe method to improve the trophicity and decrease vaginal mucosal dryness in women with vulvovaginal atrophy that developed after systemic breast cancer therapy.
癌症治疗后的生活质量保留是乳腺癌幸存者面临的主要挑战。大约 42-70%接受乳腺癌系统治疗(包括内分泌治疗)的患者会出现外阴阴道萎缩(VVA)。对于这些患者,通常建议使用基于凝胶的局部治疗方法,但这些方法具有局限性。最近,出现了一些创新的、非激素治疗方法,如激光治疗。本可行性研究旨在探讨 CO2 激光治疗既往有乳腺癌病史患者的安全性和疗效。
本前瞻性单中心研究纳入了 2017 年至 2018 年在亨利·蒙多医院接受治疗的 20 例 VVA 患者。纳入标准为阴道健康指数(VHI)评分<15 分且因乳腺癌病史而不能使用激素治疗的患者。共进行 2 次二氧化碳激光治疗。治疗采用阴道紧缩、FinePulse(脉宽 0.9ms)模式,能量密度为 11.5J/cm2,可覆盖 70%的目标阴道区域。所有患者在首次治疗后 1 个月(M1)、3 个月(M3)和 6 个月(M6)进行随访,以评估治疗对 VVA 的疗效。阴道健康指数评分和女性性困扰(FSD)评分用于评估治疗效果及其对性生活质量的影响。评分≥11 与性功能障碍相关。在基线、M1、M3 和 M6 随访时评估阴道健康指数和女性性困扰评分。
患者的平均年龄为 56.1±8.8 岁(范围,27-69 岁)。20 例患者中有 17 例(平均绝经年龄,51.25±1.5 岁)经历过绝经。纳入时,阴道健康指数和女性性困扰评分分别为 10.58±1.71 和 21.36±15.10。20 例患者中有 14 例(70%)基线时 FSD 评分≥11。在 M1 时,阴道健康指数评分显著增加至 13.42±2.3(P=0.03),与基线相比提高了 21%。在 M6 时观察到阴道健康指数评分持续显著改善,治疗后增加至 16.75±4.23(P<0.0001),与平均基线评分相比提高了 34%。M1 时女性性困扰的平均评分为 19.83±13.57,与基线评分相比下降了 7%(P<0.01)。在 M3 时,女性性困扰显著下降至 13.88±15.58,改善了 35%(P=0.006)。在 M6 时,女性性困扰评分增加至 10.35±14.7,改善了 52%(P=0.001)。在 M3 时,35%的患者女性性困扰评分>11,而在 M6 时,只有 15%的患者女性性困扰评分>11。在随访期间未报告任何副作用。
本初步可行性研究表明,CO2 激光治疗似乎是一种有效且安全的方法,可以改善既往接受乳腺癌系统治疗后出现的外阴阴道萎缩患者的营养状况并减少阴道黏膜干燥。