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质子束治疗乳腺癌再照射:多机构前瞻性 PCG 注册分析。

Proton beam therapy reirradiation for breast cancer: Multi-institutional prospective PCG registry analysis.

机构信息

Department of Radiation Oncology, Mayo Clinic, Phoenix, Arizona.

Division of Biostatistics, Health Sciences Research, Mayo Clinic, Scottsdale, Arizona.

出版信息

Breast J. 2019 Nov;25(6):1160-1170. doi: 10.1111/tbj.13423. Epub 2019 Jul 23.

Abstract

To investigate adverse events (AEs, CTCAE v4.0) and clinical outcomes for proton beam therapy (PBT) reirradiation (reRT) for breast cancer. From 2011 to 2016, 50 patients received PBT reRT for breast cancer in the prospective Proton Collaborative Group (PCG) registry. Acute AEs occurred within 180 days from start of reRT. Late AEs began or persisted beyond 180 days. Fisher's exact and Mann-Whitney rank-sum tests were utilized. Kaplan-Meier methods were used to estimate overall survival (OS) and local recurrence-free survival (LFRS). Median follow-up was 12.7 months (0-41.8). Median prior RT dose was 60 Gy (10-96.7). Median reRT dose was 55.1 Gy (45.1-76.3). Median cumulative dose was 110.6 Gy (70.6-156.8). Median interval between RT courses was 103.8 months (5.5-430.8). ReRT included regional nodes in 84% (66% internal mammary node [IMN]). Surgery included the following: 44% mastectomy, 22% wide local excision, 6% lumpectomy, 2% reduction mammoplasty, and 26% no surgery. Grade 3 AEs were experienced by 16% of patients (10% acute, 8% late) and were associated with body mass index (BMI) > 30 kg/m (P = 0.04), bilateral recurrence (P = 0.02), and bilateral reRT (P = 0.004). All grade 3 AEs occurred in patients receiving IMN reRT (P = 0.08). At 1 year, LRFS was 93%, and OS was 97%. Patients with gross disease at time of PBT trended toward worse 1-year LRFS (100% without vs. 84% with, P = 0.06). PBT reRT is well tolerated with favorable local control. BMI > 30, bilateral disease, and IMN reRT were associated with grade 3 AEs. Toxicity was acceptable despite median cumulative dose > 110 Gy.

摘要

为了研究质子束治疗(PBT)再放疗(reRT)治疗乳腺癌的不良事件(AEs,CTCAE v4.0)和临床结果。从 2011 年到 2016 年,50 名患者在质子协作组(PCG)前瞻性注册研究中接受了 PBT 再放疗。急性 AE 在 reRT 开始后 180 天内发生。迟发性 AE 在 180 天后开始或持续存在。采用 Fisher 确切概率法和 Mann-Whitney 秩和检验。Kaplan-Meier 方法用于估计总生存率(OS)和局部无复发生存率(LFRS)。中位随访时间为 12.7 个月(0-41.8)。中位既往放疗剂量为 60 Gy(10-96.7)。中位 reRT 剂量为 55.1 Gy(45.1-76.3)。中位累积剂量为 110.6 Gy(70.6-156.8)。中位放疗间隔为 103.8 个月(5.5-430.8)。再放疗包括区域淋巴结 84%(66%内乳淋巴结[IMN])。手术包括:44%乳房切除术,22%广泛局部切除术,6%保乳切除术,2%乳房缩小成形术,26%无手术。16%的患者发生 3 级 AE(10%急性,8%迟发性),与体重指数(BMI)>30 kg/m2(P=0.04)、双侧复发(P=0.02)和双侧 reRT(P=0.004)相关。所有 3 级 AE 均发生在接受 IMN reRT 的患者中(P=0.08)。1 年时,LRFS 为 93%,OS 为 97%。PBT 时存在大体疾病的患者 1 年 LRFS 趋势较差(100%无 vs. 84%有,P=0.06)。PBT reRT 耐受性良好,局部控制效果良好。BMI>30、双侧疾病和 IMN reRT 与 3 级 AE 相关。尽管累积剂量中位数>110 Gy,但毒性可接受。

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