Spanos W J, Clery M, Perez C A, Grigsby P W, Doggett R L, Poulter C A, Steinfeld A D
University of Louisville School of Medicine, KY 40202.
Int J Radiat Oncol Biol Phys. 1994 Jul 30;29(5):961-7. doi: 10.1016/0360-3016(94)90389-1.
Determine late complication incidence for pelvic palliation using accelerated multiple daily fraction radiation [Radiation Therapy Oncology Group (RTOG) 8502].
Prospective evaluation of a palliative radiation schedule for advanced pelvic malignancies was conducted from 1985 to 1989 by RTOG 8502. The dose was 44.40 Gy in 12 fractions (3.7 Gy BID) with a rest after 14.80 Gy and 29.60 Gy. The pilot part of the study allowed for a variable rest interval of 3-6 weeks. The rest interval was then randomized between 2 and 4 weeks to determine effect on tumor control. No difference in tumor control was identified (p = 0.59). The pilot segment accrued 151 patients and the randomized segment accrued 144 patients. A total of 290 cases were analyzable (four ineligible or canceled) for late effects. To minimize actuarial bias, only patients surviving 90 days (193) were analyzed for late effect risk. The primary site consisted of gynecologic (40%), colorectal (28%), genitourinary (25%), and miscellaneous (7%). The extent of tumor consisted of pelvis only (62%) and additional tumor outside the pelvis (38%). Most of the patients were elderly (76% > 60 years, 47% > 70 years). Karnofsky performance status (KPS) was > or = 80 in 60% of patients and < 80 in 40%.
None of the patients with < 30 Gy (less than three courses) developed late toxicity. A total of 11/193 (6%) developed Grade 3+ late toxicity (nine Grade 3, one Grade 4, one Grade 5). Actuarial analysis of complication rate by survival time for Grades 3, 4, and 5 shows a cumulative incidence for complications after 6 months that plateaus at 6.9% by 18 months. The cumulative incidence for Grades 4 and 5 is 2.0% by 12 months. The difference in late effect for the 2-week rest vs. 4-week rest was not statistically different (p = .47). Patient factors evaluated for increased risk of late complications included prior surgeries, age, sex, KPS and primary. None were found to have significant statistical correlations with late effects.
The crude late complications rate is 6%. Actuarial analysis using cumulative incidence shows 6.9% by 18 months. This represents a significant decrease in late complications from 49% seen with higher dose per fraction (10 Gy x 3) piloted by Radiation Therapy Oncology Group (7905) for a similar group of patients. Long-term analysis of late complication indicates this schedule can be used in the pelvis with relatively low incidence of complication. This schedule has significant logistic benefits and has been shown to produce good tumor regression and excellent palliation of symptoms.
利用加速每日多次分割放疗[放射治疗肿瘤学组(RTOG)8502]确定盆腔姑息治疗的晚期并发症发生率。
RTOG 8502在1985年至1989年对晚期盆腔恶性肿瘤的姑息性放疗方案进行了前瞻性评估。剂量为44.40 Gy,分12次(每日两次,每次3.7 Gy),在14.80 Gy和29.60 Gy后休息。研究的试点部分允许3至6周的可变休息间隔。然后将休息间隔随机分为2至4周,以确定对肿瘤控制的影响。未发现肿瘤控制方面的差异(p = 0.59)。试点部分纳入了151例患者,随机部分纳入了144例患者。共有290例病例可用于分析晚期效应(4例不符合条件或被取消)。为尽量减少精算偏差,仅对存活90天的193例患者分析晚期效应风险。原发部位包括妇科(40%)、结直肠(28%)、泌尿生殖(25%)和其他(7%)。肿瘤范围仅包括盆腔(62%)和盆腔外其他肿瘤(38%)。大多数患者为老年人(76%>60岁,47%>70岁)。60%的患者卡诺夫斯基功能状态(KPS)≥80,40%的患者KPS<80。
接受剂量<30 Gy(少于三个疗程)的患者均未出现晚期毒性。共有11/193(6%)的患者出现3级及以上晚期毒性(9例3级,1例4级,1例5级)。对3级、4级和5级并发症发生率按生存时间进行精算分析显示,6个月后并发症的累积发生率在18个月时稳定在6.9%。12个月时4级和5级并发症的累积发生率为2.0%。2周休息与4周休息的晚期效应差异无统计学意义(p = 0.47)。评估的与晚期并发症风险增加相关的患者因素包括既往手术、年龄、性别、KPS和原发部位。未发现与晚期效应有显著的统计学相关性。
粗略的晚期并发症发生率为6%。使用累积发生率的精算分析显示,18个月时为6.9%。这表明与放射治疗肿瘤学组(7905)针对类似患者群体采用的较高分次剂量(10 Gy×3)相比,晚期并发症显著减少。晚期并发症的长期分析表明,该方案可用于盆腔,并发症发生率相对较低。该方案具有显著的后勤优势,已显示出能产生良好的肿瘤退缩和出色的症状缓解效果。