le Guyader Maud, Lam Cham Kee Daniel, Thamphya Brice, Schiappa Renaud, Gautier Mathieu, Chand-Fouche Marie-Eve, Hannoun-Levi Jean-Michel
Department of Radiation Oncology, Antoine Lacassagne Cancer Center, University of Côte d'Azur, 33 avenue Valombrose, 06189 Nice Cedex 2, Nice, France.
Department of Radiation Oncology, Pôle Santé République, Clermont-Ferrand, France.
Clin Transl Radiat Oncol. 2021 Nov 6;32:15-23. doi: 10.1016/j.ctro.2021.10.005. eCollection 2022 Jan.
Brachytherapy (BT) boost after radio-chemotherapy (RCT) is a standard of care in the management of locally advanced cervical cancer (LACC). As there is no consensus on high-dose-rate (HDR) BT fractionation schemes, our aim was to report the oncological outcome and toxicity profile of four different schemes using twice-a-day (BID) HDR-BT.
This was an observational, retrospective, single institution study for patients with LACC receiving a HDR-BT boost. The latter was performed with a single implant and single imaging done on day 1. The different fractionation schemes were: 7 Gy + 4x3.5 Gy (group 1); 7 Gy + 4x4.5 Gy (group 2); 3x7Gy (group 3) and 3x8Gy (group 4). Local (LFS), nodal (NFS) and metastatic (MFS) recurrence-free survival as well as progression-free survival (PFS) and overall survival (OS) were analyzed. Acute (≤6 months) and late toxicities (>6 months) were reported.
From 2007 to 2018, 191 patients were included. Median follow-up was 57 months [45-132] and median EQD2DCTV was 84, 82 and 90 Gy for groups 2, 3 and 4 respectively (dosimetric data missing for group 1). The 5-year LFS, NFS, MFS, PFS and OS were 85% [81-90], 83% [79-86], 70% [67-73], 61% [57-64] and 75% [69-78] respectively, with no significant difference between the groups. EQD2DCTV < 85 Gy was a prognostic factor for local recurrence in univariate analysis (p = 0.045). The rates of acute/late grade ≥ 2 urinary, digestive and gynecological toxicities were 9%/15%, 3%/15% and 9%/25% respectively.
Bi-fractionated HDR-BT boost seems feasible with good oncological outcome and slightly more toxicity after dose escalation.
放化疗(RCT)后近距离放疗(BT)强化是局部晚期宫颈癌(LACC)治疗的标准方案。由于高剂量率(HDR)BT分割方案尚无共识,我们的目的是报告采用每日两次(BID)HDR - BT的四种不同方案的肿瘤学结局和毒性特征。
这是一项针对接受HDR - BT强化治疗的LACC患者的观察性、回顾性、单机构研究。后者通过单次植入和第1天的单次成像进行。不同的分割方案为:7 Gy + 4×3.5 Gy(第1组);7 Gy + 4×4.5 Gy(第2组);3×7 Gy(第3组)和3×8 Gy(第4组)。分析局部(LFS)、区域(NFS)和远处转移(MFS)无复发生存率以及无进展生存率(PFS)和总生存率(OS)。报告急性(≤6个月)和晚期毒性(>6个月)。
2007年至2018年,纳入191例患者。中位随访时间为57个月[45 - 132],第2、3和4组的中位等效剂量2(EQD2)DCTV分别为84、82和90 Gy(第1组剂量学数据缺失)。5年LFS、NFS、MFS、PFS和OS分别为85% [81 - 90]、83% [79 - 86]、70% [67 - 73]、61% [57 - 64]和75% [69 - 78],各组间无显著差异。单因素分析中,EQD2 DCTV < 85 Gy是局部复发的预后因素(p = 0.045)。急性/晚期≥2级泌尿、消化和妇科毒性发生率分别为9%/15%、3%/15%和9%/25%。
两次分割的HDR - BT强化似乎可行,肿瘤学结局良好,剂量增加后毒性略高。