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分次半身照射(HBI)用于快速缓解广泛、有症状的转移性骨病:国际原子能机构(IAEA)的一项随机III期试验。

Fractionated half-body irradiation (HBI) for the rapid palliation of widespread, symptomatic, metastatic bone disease: a randomized Phase III trial of the International Atomic Energy Agency (IAEA).

作者信息

Salazar O M, Sandhu T, da Motta N W, Escutia M A, Lanzós-Gonzales E, Mouelle-Sone A, Moscol A, Zaharia M, Zaman S

机构信息

Department of Radiation Oncology and Cancer Center, Oakwood Healthcare System, Dearborn, MI 48123-2500, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2001 Jul 1;50(3):765-75. doi: 10.1016/s0360-3016(01)01495-x.

Abstract

PURPOSE

To find the fastest and most effective/efficient method to economically deliver fractionated half-body irradiation (HBI) for widespread (WS), symptomatic, metastatic bone cancer.

METHODS AND MATERIALS

A Phase III trial with 3 HBI arms: (Arm A) Control (15 Gy/5 fractions/5 days); (Arm B) Hyperfractionation (HF) (8 Gy/2 fractions/1 day); (Arm C) Accelerated HF (12 Gy/4 fractions/2 days). Six countries randomized 156 patients (all with WS bone metastases): 51, 56, and 49 patients to Arms A, B, and C, respectively. There were 72 (46%) breast, 50 (32%) prostate, 9 (6%) lung, and 25 (16%) miscellaneous primary tumors. Initial performance status (PS) was 1-2 in 101 (65%) and PS 3-4 in 55 (35%). The lower, upper, and middle halves of the body were treated 79, 68, and 9 times.

RESULTS

Pain relief was seen in 91% of patients (45% complete [CR] and 46% partial [PR]) within 3-8 days. Overall (OS), median (MST), and pain-free (PFS) survival was 174, 150, and 122 days. Breast tumors had a higher OS (279 days) than that of other primary tumors, but when analyzed by treatment, was not significantly different than prostate tumors in Arm A. No survival differences were found in patients with PS 1-2 vs. 3-4, CR vs. PR, bone with/without visceral metastases, or by the number of metastases (< or > 15 bone lesions). Quality of life (QOL) assessed by the percent of the remaining life free of pain was 71%; furthermore significant improvements in PS, pain, and narcotic scores were seen after HBI. Toxicity was very acceptable (41% none, 50% mild/moderate, 12% severe but transitory); more was seen with upper HBI.

CONCLUSION

In terms of response, time to response, OS, MST, PFS, QOL, and toxicity, schedules for Arms A and C were similar for all but prostate primaries. Schedule for Arm B, which delivered the lowest biologic dose in the shortest time, had significantly worse results in pain relief, OS, MST, PFS, and QOL. Results indicate that, for most primary tumor types (except prostate), delivering two HBI daily doses of 3 Gy in 2 consecutive days is as effective as delivering a daily dose of 3 Gy for 5 consecutive days. Thus, this is a faster and much more convenient HBI schedule for the palliation of pain in widespread cancer.

摘要

目的

寻找一种经济高效的方法,为广泛播散(WS)、有症状的转移性骨癌进行分次半身照射(HBI)。

方法和材料

一项III期试验,有3个HBI组:(A组)对照组(15 Gy/5次/5天);(B组)超分割(HF)组(8 Gy/2次/1天);(C组)加速超分割组(12 Gy/4次/2天)。6个国家将156例患者(均为WS骨转移患者)随机分组:分别有51、56和49例患者进入A、B、C组。原发性肿瘤中,乳腺癌72例(46%)、前列腺癌50例(32%)、肺癌9例(6%)、其他原发性肿瘤25例(16%)。初始体能状态(PS)为1 - 2级的有101例(65%),PS为3 - 4级的有55例(35%)。身体下半部、上半部和中部接受治疗的次数分别为79次、68次和9次。

结果

91%的患者在3 - 8天内疼痛缓解(45%完全缓解[CR],46%部分缓解[PR])。总生存期(OS)、中位生存期(MST)和无痛生存期(PFS)分别为174天、150天和122天。乳腺癌患者的OS(279天)高于其他原发性肿瘤患者,但按治疗组分析时,与A组前列腺癌患者无显著差异。PS为1 - 2级与3 - 4级的患者、CR与PR的患者、有/无内脏转移的骨转移患者或转移灶数量(<或>15个骨病灶)不同的患者之间,未发现生存差异。通过剩余无痛生活百分比评估的生活质量(QOL)为71%;此外,HBI后PS、疼痛和麻醉评分有显著改善。毒性反应非常可接受(41%无毒性反应,50%为轻/中度,仅12%为严重但短暂的毒性反应);上半身HBI的毒性反应更多。

结论

在反应、反应时间、OS、MST、PFS、QOL和毒性方面,除前列腺原发性肿瘤外,A组和C组的方案相似。B组方案在最短时间内给予的生物剂量最低,在疼痛缓解、OS、MST、PFS和QOL方面的结果明显较差。结果表明,对于大多数原发性肿瘤类型(前列腺癌除外),连续2天每天给予2次HBI剂量3 Gy与连续5天每天给予剂量3 Gy的效果相同。因此,这是一种更快且更方便的HBI方案,用于缓解广泛播散性癌症的疼痛。

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