Sibley G S, Jamieson T A, Marks L B, Anscher M S, Prosnitz L R
Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27516, USA.
Int J Radiat Oncol Biol Phys. 1998 Jan 1;40(1):149-54. doi: 10.1016/s0360-3016(97)00589-0.
To review our experience treating clinical Stage I non-small-cell lung carcinoma with radiotherapy alone using modern techniques and staging. The effect of dose and volume on outcome is to be analyzed.
Between January 1980 and December 1995, 156 patients with Stage I medically inoperable non-small-cell lung cancer were irradiated at Duke University Medical Center and the Durham Veterans Administration Medical Center. Fifteen patients were excluded from analysis (7 treated with palliative intent, and 8 lost to follow-up immediately following radiation). Characteristics of the 141 evaluable patients were as follows: Median age 70 years (range 46-95); gender: male 83%, female 17%; institution: DUMC 65%, DVAMC 35%; T1N0 54%, T2N0 46%; median size 3 cm (range 0.5 to 8); pathology: squamous cell carcinoma 52%, adenocarcinoma 18%, large cell carcinoma 19%, not otherwise specified 11%; presenting symptoms: weight loss 26%, cough 23%, none (incidental diagnosis) 57%. All patients underwent simulation prior to radiotherapy using linear accelerators of > or = 4 MV. No patients received surgery or chemotherapy as part of their initial treatment. The median dose of radiotherapy (not reflecting lung inhomogeneity corrections) was 64 Gy (50 to 80 Gy) given in 1.2 bid to 3 Gy qid fractionation. The majority of cases included some prophylactic nodal regions (73%).
Of the 141 patients, 108 have died; 33% of intercurrent death, 35% of cancer, and 7% of unknown causes. At last follow-up, 33 patients were alive (median 24 months, range 7-132 months). The 2- and 5-year overall survival was 39% and 13%, respectively (median 18 months). The corresponding cause-specific survival was 60%, and 32% (median 30 months). On multivariate analysis, significant factors influencing overall and/or cause-specific survival were age, squamous cell histology, incidental diagnosis, and pack-years of smoking. There was a nonsignificant trend towards improved cause-specific survival with higher radiotherapy doses and larger treatment volumes. On patterns of failure analysis, 42% of failures were local-only and 38% were distant-only. Regional-only failure occurred in 4 patients (7%), 3 of whom failed solely in an unirradiated nodal site. Analysis of factors correlating with local failure at 2 years was performed using a multinominal logistic regression analysis. Significant factors associated with a lower local failure included incidental diagnosis and absence of cough with a strong trend toward significance for higher radiotherapy dose (p = 0.07) and larger treatment volume (p = 0.08). Patients who were locally controlled had an improved cause-specific survival at 5 years over those who were not controlled (46% vs. 12%, p = 0.03). Grade III-V complications occurred in 2 patients (1.5%).
Patients with clinical Stage I medically inoperable non-small-cell lung cancer treated with contemporary radiotherapy alone achieved a 5-year cause-specific survival of 32%. Uncontrolled lung cancer was the primary cause of death in these patients, and local failure alone represented the most common mode of failure (42%). Patients who were locally controlled had a significantly improved cause-specific survival over those who failed locally. Because higher doses of radiotherapy appear to provide improved local control, studies of dose escalation are warranted until dose-limiting toxicity is observed.
回顾我们使用现代技术和分期方法单纯放疗治疗临床I期非小细胞肺癌的经验。分析剂量和体积对治疗结果的影响。
1980年1月至1995年12月期间,156例I期医学上无法手术的非小细胞肺癌患者在杜克大学医学中心和达勒姆退伍军人事务医疗中心接受了放疗。15例患者被排除在分析之外(7例为姑息性治疗,8例放疗后失访)。141例可评估患者的特征如下:中位年龄70岁(范围46 - 95岁);性别:男性83%,女性17%;机构:杜克大学医学中心65%,达勒姆退伍军人事务医疗中心35%;T1N0 54%,T2N0 46%;中位大小3 cm(范围0.5至8 cm);病理:鳞状细胞癌52%,腺癌18%,大细胞癌19%,未另行分类11%;出现的症状:体重减轻26%,咳嗽23%,无(偶然诊断)57%。所有患者在放疗前使用≥4 MV的直线加速器进行模拟定位。所有患者初始治疗均未接受手术或化疗。放疗的中位剂量(未反映肺部不均匀性校正)为64 Gy(50至80 Gy),采用每日两次1.2 Gy至每日四次3 Gy的分割方式。大多数病例包括一些预防性淋巴结区域(73%)。
141例患者中,108例死亡;33%死于并发疾病,35%死于癌症,7%死因不明。在最后一次随访时,33例患者存活(中位生存期24个月,范围7 - 132个月)。2年和5年总生存率分别为39%和13%(中位生存期18个月)。相应的病因特异性生存率分别为60%和32%(中位生存期30个月)。多因素分析显示,影响总生存和/或病因特异性生存的显著因素为年龄、鳞状细胞组织学类型、偶然诊断以及吸烟包年数。放疗剂量增加和治疗体积增大有使病因特异性生存改善的非显著趋势。在失败模式分析中,42%的失败为仅局部复发,38%为仅远处复发。仅区域复发发生在4例患者中(7%),其中3例仅在未照射的淋巴结部位复发。使用多项逻辑回归分析对与2年局部失败相关的因素进行分析。与较低局部失败相关的显著因素包括偶然诊断和无咳嗽,放疗剂量增加(p = 0.07)和治疗体积增大(p = 0.08)有显著趋势。局部得到控制的患者5年病因特异性生存率高于未得到控制的患者(46%对12%,p = 0.03)。2例患者(1.5%)发生III - V级并发症。
单纯采用现代放疗技术治疗临床I期医学上无法手术的非小细胞肺癌患者,5年病因特异性生存率为32%。未控制的肺癌是这些患者的主要死亡原因,仅局部失败是最常见的失败模式(42%)。局部得到控制的患者病因特异性生存率显著高于局部失败的患者。由于更高剂量的放疗似乎能改善局部控制,在观察到剂量限制性毒性之前,有必要进行剂量递增研究。