Rudra Soumon, Roy Amit, Brenneman Randall, Gabani Prashant, Roach Michael C, Ochoa Laura, Prather Heidi, Appleton Catherine, Margenthaler Julie, Peterson Lindsay L, Bagegni Nusayba A, Zoberi Jacqueline E, Garcia-Ramirez Jose, Thomas Maria A, Zoberi Imran
Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri.
Adv Radiat Oncol. 2020 Oct 27;6(1):100602. doi: 10.1016/j.adro.2020.10.015. eCollection 2021 Jan-Feb.
Our purpose was to describe the risk of radiation-induced brachial plexopathy (RIBP) in patients with breast cancer who received comprehensive adjuvant radiation therapy (RT).
Records for 498 patients who received comprehensive adjuvant RT (treatment of any residual breast tissue, the underlying chest wall, and regional nodes) between 2004 and 2012 were retrospectively reviewed. All patients were treated with conventional 3 to 5 field technique (CRT) until 2008, after which intensity modulated RT (IMRT) was introduced. RIBP events were determined by reviewing follow-up documentation from oncologic care providers. Patients with RIBP were matched (1:2) with a control group of patients who received CRT and a group of patients who received IMRT. Dosimetric analyses were performed in these patients to determine whether there were differences in ipsilateral brachial plexus dose distribution between RIBP and control groups.
Median study follow-up was 88 months for the overall cohort and 92 months for the IMRT cohort. RIBP occurred in 4 CRT patients (1.6%) and 1 IMRT patient (0.4%) ( = .20). All patients with RIBP in the CRT cohort received a posterior axillary boost. Maximum dose to the brachial plexus in RIBP, CRT control, and IMRT control patients had median values of 56.0 Gy (range, 49.7-65.1), 54.8 Gy (47.4-60.5), and 54.8 Gy (54.2-57.3), respectively.
RIBP remains a rare complication of comprehensive adjuvant breast radiation and no clear dosimetric predictors for RIBP were identified in this study. The IMRT technique does not appear to adversely affect the development of this late toxicity.
我们的目的是描述接受综合辅助放疗(RT)的乳腺癌患者发生放射性臂丛神经病变(RIBP)的风险。
回顾性分析了2004年至2012年间接受综合辅助RT(治疗任何残留乳腺组织、胸壁及区域淋巴结)的498例患者的记录。2008年之前所有患者均采用传统的3至5野技术(CRT)治疗,之后引入调强放疗(IMRT)。通过查阅肿瘤护理提供者的随访记录来确定RIBP事件。将发生RIBP的患者与接受CRT的对照组患者以及接受IMRT的患者组(1:2)进行匹配。对这些患者进行剂量分析,以确定RIBP组与对照组同侧臂丛神经剂量分布是否存在差异。
整个队列的中位研究随访时间为88个月,IMRT队列的中位随访时间为92个月。4例CRT患者(1.6%)和1例IMRT患者(0.4%)发生RIBP(P = 0.20)。CRT队列中所有发生RIBP的患者均接受了腋窝后野加量照射。RIBP患者、CRT对照组患者和IMRT对照组患者臂丛神经的最大剂量中位数分别为56.0 Gy(范围49.7 - 65.1)、54.8 Gy(47.4 - 60.5)和54.8 Gy(54.2 - 57.3)。
RIBP仍然是综合辅助乳腺放疗的一种罕见并发症,本研究未发现RIBP明确的剂量学预测因素。IMRT技术似乎不会对这种晚期毒性的发生产生不利影响。