Hanks G E, Hanlon A L, Schultheiss T E, Pinover W H, Movsas B, Epstein B E, Hunt M A
Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Int J Radiat Oncol Biol Phys. 1998 Jun 1;41(3):501-10. doi: 10.1016/s0360-3016(98)00089-3.
To report the 5-year outcomes of dose escalation with 3D conformal treatment (3DCRT) of prostate cancer.
Two hundred thirty-two consecutive patients were treated with 3DCRT alone between 6/89 and 10/92 with ICRU reporting point dose that increased from 63 to 79 Gy. The median follow-up was 60 months, and any patient free of clinical or biochemical evidence of disease was termed bNED. Biochemical failure was defined as prostate-specific antigen (PSA) rising on two consecutive recordings and exceeding 1.5 ng/ml. Morbidity was reported by the Radiation Therapy Oncology Group (RTOG) scale, the Late Effects Normal Tissue (LENT) scale, and a Fox Chase modification of the latter (FC-LENT). All patients were treated with a four-field technique with a 1 cm clinical target volume (CTV) to planning target volume (PTV) margin to the prostate or prostate boost; the CTV and gross tumor volume (GTV) were the same. Actuarial rates of outcome were calculated by Kaplan-Meier and cumulative incidence methods and compared using the log rank and Gray's test statistic, respectively. Cox regression models were used to establish prognostic factors predictive of the various measures of outcome. Five-year Kaplan-Meier bNED rates were utilized by dose group to estimate logit response models for bNED and late morbidity.
PSA <10 ng/ml: No dose response was demonstrated using estimated bNED rates or by analysis of PSA nadir vs. dose. PSA 10-19.9 ng/ml: A bNED dose response was demonstrated (p = 0.02) using the log rank test. The logit response model showed 5-year bNED rates of 35% at 70 Gy and 75% at 76 Gy (p = 0.0049) and illustrated the relative ineffectiveness of conventional dose treatment. PSA 20+ ng/ml: A bNED dose response was demonstrated (p = 0.02) using the log rank test. The logit response model indicated a 5-year bNED rate of 10% at 70 Gy and 32% at 76 Gy (p = 0.10). Morbidity: Dose response was demonstrated for FC-LENT grade 2 and grade 3,4 GI morbidity and for LENT grade 2 GU sequelae. RTOG grade 3,4 GI morbidity at 5 years was <1%. Factors associated with bNED, cause-specific survival, and metastasis were studied using Cox multivariate analysis. Pretreatment PSA (p = 0.0001), Gleason score 7-10 (p = 0.0001), and dose (p = 0.017) were significantly predictive of bNED. For each 1 Gy increase in dose, the hazard of bNED failure decreased by 8%. Palpation stage was associated with cause-specific survival (p = 0.002) and distant metastasis (p = 0.0004). Gleason score was also predictive of distant metastasis (p = 0.02).
A dose response was observed for patients with pretreatment PSA >10 ng/ml based on 5-year bNED results. No dose response was observed for patients with pretreatment PSA < 10 ng/ml. Dose response was observed for FC-LENT grade 2 and grade 3,4 GI sequelae and for LENT grade 2 GU sequelae. Optimization of treatment was made possible by the results in this report. The improvement in 5-year bNED rates for patients with PSA levels > 10 ng/ml strongly suggests that clinical trials employing radiation should investigate the use of 3DCRT and prostate doses of 76-80 Gy.
报告前列腺癌三维适形治疗(3DCRT)剂量递增的5年结果。
1989年6月至1992年10月期间,连续232例患者接受单纯3DCRT治疗,国际辐射单位与测量委员会(ICRU)报告点剂量从63 Gy增至79 Gy。中位随访时间为60个月,任何无疾病临床或生化证据的患者被称为生化无疾病证据(bNED)。生化失败定义为前列腺特异性抗原(PSA)连续两次检测升高且超过1.5 ng/ml。发病率采用放射肿瘤学组(RTOG)标准、正常组织晚期效应(LENT)标准以及后者的福克斯蔡斯修正版(FC-LENT)进行报告。所有患者均采用四野技术治疗,临床靶区(CTV)至计划靶区(PTV)边缘距离前列腺或前列腺增敏区为1 cm;CTV与大体肿瘤体积(GTV)相同。采用Kaplan-Meier法和累积发病率法计算结局的精算率,并分别使用对数秩检验和Gray检验统计量进行比较。采用Cox回归模型建立预测各种结局指标的预后因素。利用剂量组的5年Kaplan-Meier bNED率来估计bNED和晚期发病率的对数反应模型。
PSA<10 ng/ml:使用估计的bNED率或通过分析PSA最低点与剂量,未显示剂量反应。PSA 10 - 19.9 ng/ml:使用对数秩检验显示bNED剂量反应(p = 0.02)。对数反应模型显示,70 Gy时5年bNED率为35%,76 Gy时为75%(p = 0.0049),并说明了传统剂量治疗的相对无效性。PSA≥20 ng/ml:使用对数秩检验显示bNED剂量反应(p = 0.02)。对数反应模型表明,70 Gy时5年bNED率为10%,76 Gy时为32%(p = 0.10)。发病率:FC-LENT 2级和3、4级胃肠道发病率以及LENT 2级泌尿生殖系统后遗症显示有剂量反应。5年时RTOG 3、4级胃肠道发病率<1%。使用Cox多变量分析研究与bNED、特定病因生存率和转移相关的因素。治疗前PSA(p = 0.0001)、Gleason评分7 - 10(p = 0.0001)和剂量(p = 0.017)是bNED的显著预测因素。剂量每增加1 Gy,bNED失败的风险降低8%。触诊分期与特定病因生存率(p = 0.002)和远处转移(p = 0.0004)相关。Gleason评分也是远处转移的预测因素(p = 0.02)。
根据5年bNED结果,观察到治疗前PSA>10 ng/ml的患者有剂量反应。治疗前PSA<10 ng/ml的患者未观察到剂量反应。观察到FC-LENT 2级和3、4级胃肠道后遗症以及LENT 2级泌尿生殖系统后遗症有剂量反应。本报告的结果使治疗优化成为可能。PSA水平>10 ng/ml患者5年bNED率的提高强烈表明,采用放疗的临床试验应研究3DCRT和76 - 80 Gy前列腺剂量的应用。