Breast Care Specialists, Bethpage, NY, USA.
Department of Radiation Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH, USA.
Breast Cancer Res Treat. 2017 Dec;166(3):809-815. doi: 10.1007/s10549-017-4451-x. Epub 2017 Aug 22.
This analysis was performed to assess the impact of early intervention following prospective surveillance using bioimpedance spectroscopy (BIS) to detect and manage breast cancer-related lymphedema (BCRL).
From 8/2010 to 12/2016, 206 consecutive patients were evaluated with BIS. The protocol included pre-operative assessment with L-Dex as well as post-operative assessments at regular intervals. Patients with L-Dex scores >10 from baseline were considered to have subclinical BCRL and were treated with over-the-counter (OTC) compression sleeve for 4 weeks. High-risk patients were defined as undergoing axillary lymph node dissection (ALND), receiving regional nodal irradiation (RNI), or taxane chemotherapy. Chronic BCRL was defined as the need for complex decongestive physiotherapy (CDP).
Median follow-up was 25.9 months. Overall, 17% of patients had one high-risk feature, 8% two, and 7% had three. 9.8% of patients were diagnosed with subclinical BCRL with highest rates seen following ALND (23 vs. 7%, p = 0.01). Development of subclinical BCRL was associated with ALND and receipt of RNI. At last follow-up, no patients (0%) developed chronic, clinically detectable, BCRL. Subset analysis was performed of the 30 patients undergoing ALND. Median number of nodes removed was 18 and median number of positive nodes was 2. 77% received taxane chemotherapy, 62% axillary RT, and 48% had elevated BMI. Overall, 86% of patients had at least one additional high-risk feature, 70% at least two, and 23% had all three. Seven patients (23%) had abnormally elevated L-Dex scores at some point during follow-up. To date, none has required CDP.
The results of this study support prospective surveillance utilizing BIS initiated pre-operatively with subsequent post-operative follow-up measurements for the detection of subclinical BCRL. Intervention triggered by subclinical BCRL detection with an elevated L-Dex score was associated with no cases progressing to chronic, clinically detectable BCRL even in very high-risk patients.
本分析旨在评估前瞻性监测后早期干预对乳腺癌相关淋巴水肿(BCRL)的影响。前瞻性监测采用生物阻抗谱(BIS)来检测和管理 BCRL。
2010 年 8 月至 2016 年 12 月,连续评估了 206 例患者。该方案包括术前使用 L-Dex 评估以及定期术后评估。基线时 L-Dex 评分>10 的患者被认为患有亚临床 BCRL,并接受非处方(OTC)压缩袖套治疗 4 周。高危患者定义为接受腋窝淋巴结清扫术(ALND)、接受区域淋巴结照射(RNI)或紫杉烷化疗。慢性 BCRL 定义为需要复杂消肿物理治疗(CDP)。
中位随访时间为 25.9 个月。总体而言,17%的患者有 1 个高危特征,8%的患者有 2 个,7%的患者有 3 个。9.8%的患者被诊断为亚临床 BCRL,其中 ALND 后发生率最高(23%比 7%,p=0.01)。亚临床 BCRL 的发展与 ALND 和 RNI 的应用相关。末次随访时,无患者(0%)发生慢性、临床可检测的 BCRL。对接受 ALND 的 30 例患者进行了亚组分析。中位切除淋巴结数为 18 个,阳性淋巴结中位数为 2 个。77%的患者接受了紫杉烷化疗,62%的患者接受了腋窝放疗,48%的患者 BMI 升高。总体而言,86%的患者至少有 1 个其他高危特征,70%的患者至少有 2 个,23%的患者有 3 个。7 名患者(23%)在随访过程中的某个时间点 L-Dex 评分异常升高。迄今为止,尚无患者需要接受 CDP。
本研究结果支持在术前进行前瞻性监测,利用 BIS 检测亚临床 BCRL,并在术后进行后续随访测量。亚临床 BCRL 检测触发的干预措施,通过升高的 L-Dex 评分,即使在高危患者中,也没有导致慢性、临床可检测的 BCRL 进展。