Bjørnholt Sarah M, Groenvold Mogens, Petersen Morten A, Mogensen Ole, Bouchelouche Kirsten, Sponholtz Sara E, Neumann Gudrun, Bjørn Signe F, Hamid Bushra H, Dahl Katja, Jensen Pernille T
Department of Gynaecology and Obstetrics, Aarhus University Hospital, Aarhus N, Denmark; Institute of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus N, Denmark.
Department of Public Health, University of Copenhagen, KøbCenhavn, Denmark; Palliative Care Research Unit, Bispebjerg and Frederiksberg Hospital, University of Copenhagen, Copenhagen NV, Denmark.
Am J Obstet Gynecol. 2025 Mar;232(3):306.e1-306.e11. doi: 10.1016/j.ajog.2024.09.001. Epub 2024 Sep 6.
Sentinel lymph node mapping is a minimally invasive surgical staging procedure that allows identification of macro- and micrometastases. The implementation of sentinel lymph node mapping to women with low-grade endometrial cancer allows detection of lymph node metastases and avoids the morbidity of radical pelvic lymphadenectomy. The extent of myometrial invasion is highly predictive of lymph node metastases but is hard to determine precisely preoperatively. The exact rate of lymph node metastases in the large group of women with <50% myometrial invasion is low but unknown. The benefit of detecting metastases in this group should balance the risk of lymphedema. There is limited knowledge of early and late lymphedema and its impact on the quality of life in women with low-grade endometrial cancer following sentinel lymph node mapping.
The primary objective was to investigate the risk of patient-reported lymphedema after sentinel lymph node mapping in women with low-grade endometrial cancer. In addition, we aimed to evaluate risk factors for lymphedema and the condition-specific quality of life (QoL) among women who reported lymphedema 12 months after surgery.
Women with presumed stage I low-grade endometrial cancer were included in a national prospective cohort study on sentinel lymph node mapping from March 2017 to February 2022. Women completed a package of validated patient-reported outcome measures before surgery, 3 and 12 months after surgery. The primary outcome was the leg lymphedema domain score from the European Organisation for Research and Treatment of Cancer-Endometrial Cancer Module (EORTC QLQ-EN24). The lymphedema assessment was further supplemented by 7 validated single items from the European Organisation for Research and Treatment of Cancer item library addressing lymphedema of legs, genitals, and groin. The disease-specific quality of life was assessed using the validated Lymphedema Quality of Life Tool. Scores were linearly transformed to 0 to 100. A change from baseline of 8 points in leg lymphedema sum-score was considered clinically important. Mean difference scores over time with 95% confidence interval were estimated. Multiple linear regression models evaluated baseline predictors associated with the 12 months postoperative lymphedema score, and if early lymphedema predicted lymphedema at 12 months after surgery. Lymphedema condition-specific quality of life was evaluated for women with lymphedema.
Seventy-nine % (486/617) completed patient-reported outcome measures at baseline and 12 months. The mean difference score of leg lymphedema from baseline to 12 months was 5.0, confidence interval [3.3, 6.8], that is, below the threshold for clinical importance. Baseline leg lymphedema score and body mass index were positively associated with the leg lymphedema score at 12 months. The leg lymphedema score at 3 months was associated with a higher 12-month score. High scores of lymphedema at 12 months were negatively associated with the women's daily activities, appearance, emotional functioning, and global quality of life and increased their subjective symptom burden.
Women with low-grade endometrial cancer have a low risk of lymphedema after sentinel lymph node mapping. Leg swelling at baseline and body mass index predicted more lymphedema at 12 months after surgery. Early lymphedema at 3 months predicted persistent lymphedema. A high leg lymphedema score at 12 months is associated with impairment in several aspects of quality of life.
前哨淋巴结定位是一种微创手术分期方法,可用于识别宏观和微观转移灶。对低级别子宫内膜癌女性实施前哨淋巴结定位可检测出淋巴结转移,并避免根治性盆腔淋巴结清扫术的并发症。肌层浸润程度对淋巴结转移具有高度预测性,但术前很难精确确定。在肌层浸润<50%的大量女性中,淋巴结转移的确切发生率较低,但尚不清楚。在该组中检测转移灶的益处应与淋巴水肿风险相平衡。对于前哨淋巴结定位术后的低级别子宫内膜癌女性,早期和晚期淋巴水肿及其对生活质量的影响的相关知识有限。
主要目的是调查低级别子宫内膜癌女性前哨淋巴结定位术后患者报告的淋巴水肿风险。此外,我们旨在评估淋巴水肿的风险因素以及术后12个月报告有淋巴水肿的女性的特定疾病生活质量(QoL)。
2017年3月至2022年2月,将疑似I期低级别子宫内膜癌的女性纳入一项关于前哨淋巴结定位的全国前瞻性队列研究。女性在手术前、术后3个月和12个月完成一套经过验证的患者报告结局测量。主要结局是欧洲癌症研究与治疗组织-子宫内膜癌模块(EORTC QLQ-EN24)中的腿部淋巴水肿领域评分。淋巴水肿评估还通过欧洲癌症研究与治疗组织项目库中的7项经过验证的单项进行补充,这些单项涉及腿部、生殖器和腹股沟的淋巴水肿。使用经过验证的淋巴水肿生活质量工具评估特定疾病的生活质量。分数线性转换为0至100。腿部淋巴水肿总分从基线变化8分被认为具有临床意义。估计随时间变化的平均差异分数及其95%置信区间。多元线性回归模型评估与术后12个月淋巴水肿评分相关的基线预测因素,以及早期淋巴水肿是否可预测术后12个月的淋巴水肿。对有淋巴水肿的女性评估淋巴水肿特定疾病的生活质量。
79%(486/617)的女性在基线和12个月时完成了患者报告结局测量。从基线到12个月,腿部淋巴水肿的平均差异分数为5.0,置信区间为[3.3, 6.8],即低于临床重要性阈值。基线腿部淋巴水肿评分和体重指数与12个月时的腿部淋巴水肿评分呈正相关。3个月时的腿部淋巴水肿评分与12个月时较高的评分相关。12个月时淋巴水肿高分与女性的日常活动、外观、情绪功能和总体生活质量呈负相关,并增加了她们的主观症状负担。
低级别子宫内膜癌女性在前哨淋巴结定位术后发生淋巴水肿的风险较低。基线时腿部肿胀和体重指数可预测术后12个月更多的淋巴水肿。3个月时的早期淋巴水肿可预测持续性淋巴水肿。12个月时较高的腿部淋巴水肿评分与生活质量的多个方面受损相关。