Baumann Pia, Nyman Jan, Lax Ingmar, Friesland Signe, Hoyer Morten, Rehn Ericsson Suzanne, Johansson Karl-Axel, Ekberg Lars, Morhed Elisabeth, Paludan Merete, Wittgren Lena, Blomgren Henrik, Lewensohn Rolf
Division of Oncology and Hospital Physics, Radiumhemmet Karolinska University Hospital, Sweden.
Acta Oncol. 2006;45(7):787-95. doi: 10.1080/02841860600904862.
We reviewed results of SBRT treatment of 138 patients with medically inoperable stage I NSCLC treated during 1996-2003 at five different centres in Sweden and Denmark. Mean age was 74 years (range 56-90) with 69 men and 72 women. SBRT was delivered using a 3D conformal multifield technique and a stereotactic body frame. Doses delivered were 30-48 Gy (65% isodose at the periphery of planning target volume, PTV) in 2-4 fractions. Equivalent dose in 2 Gy fractions (EQD2) was in the range of 50-100 Gy. Mean gross tumour volume (GTV) was 39 cm3 (2-436), and planning target volume was 101 cm3 (11-719). Overall response rate (CR, PR) was 61% (84/138). SD was noted in 36% (50/138). During a median follow-up period of 33 months (1-107), 16 (12%) local failures occurred, ten of which also included distant metastases. Local failure was associated with tumour size, target definition and central or pleura proximity. Distant metastases occurred in 25% (35/138) of the patients. Ninety-one (65%) patients died during follow-up of which 55 patients (60%) died of other causes than lung cancer. Three- and 5-year overall survival was 52 and 26% respectively. Lung cancer specific 3- and 5-year overall survival was 66 and 40% respectively. Fifty nine percent (83/138) of the patients had no side effects. Fourteen patients experienced grade 3-4 toxicity according to radiation therapy oncology group (RTOG). EQD2 (> v.s.<55.6 Gy) showed a statistically significant benefit survival for the higher doses. SBRT for stage I NSCLC results in favourable local control not inferior to fractionated RT and with acceptable toxicity.
我们回顾了1996年至2003年期间在瑞典和丹麦五个不同中心接受立体定向体部放射治疗(SBRT)的138例医学上无法手术的I期非小细胞肺癌(NSCLC)患者的治疗结果。平均年龄为74岁(范围56 - 90岁),其中男性69例,女性72例。SBRT采用三维适形多野技术和立体定向体架进行。给予的剂量为30 - 48 Gy(计划靶区(PTV)周边65%等剂量线),分2 - 4次给予。2 Gy分割的等效剂量(EQD2)范围为50 - 100 Gy。平均肿瘤总体积(GTV)为39 cm³(2 - 436),计划靶区体积为101 cm³(11 - 719)。总缓解率(完全缓解,部分缓解)为61%(84/138)。疾病稳定(SD)见于36%(50/138)的患者。在中位随访期33个月(1 - 107个月)内,发生16例(12%)局部复发,其中10例还伴有远处转移。局部复发与肿瘤大小、靶区定义以及靠近中央或胸膜有关。25%(35/138)的患者发生远处转移。91例(65%)患者在随访期间死亡,其中55例(60%)死于肺癌以外的其他原因。3年和5年总生存率分别为52%和26%。肺癌特异性3年和5年总生存率分别为66%和40%。59%(83/138)的患者无副作用。根据放射肿瘤学组(RTOG)标准,14例患者出现3 - 4级毒性反应。EQD2(> vs. <55.6 Gy)显示高剂量组在生存方面有统计学显著益处。I期NSCLC的SBRT可实现良好的局部控制,不劣于分割放疗,且毒性可接受。