Wulf Joern, Haedinger Ulrich, Oppitz Ulrich, Thiele Wibke, Mueller Gerd, Flentje Michael
Department of Radiotherapy, University of Wuerzburg, Josef-Schneider-Strasse 11, D-97080 Wuerzburg, Germany.
Int J Radiat Oncol Biol Phys. 2004 Sep 1;60(1):186-96. doi: 10.1016/j.ijrobp.2004.02.060.
The clinical results of dose escalation using stereotactic radiotherapy to increase local tumor control in medically inoperable patients with Stage I-II non-small-cell lung cancer or pulmonary metastases were evaluated.
Twenty patients with Stage I-II non-small-cell lung cancer and 41 patients with 51 pulmonary metastases not amenable to surgery were treated with stereotactic radiotherapy at 3 x 10 Gy (n = 19), 3 x 12-12.5 Gy to the planning target volume enclosing 100%-isodose, with normalization to 150% at the isocenter; n = 26) or 1 x 26 Gy to the planning target volume enclosing 80%-isodose (n = 26). The median follow-up was 11 months (range, 2-61 months) for primary lung cancer patients and 9 months (range, 2-37 months) for patients with metastases.
The actuarial local control rate was 92% for lung cancer patients and 80% for metastasis patients > or =1 year after treatment and was significantly improved by increasing the dose from 3 x 10 Gy to 3 x 12-12.5 Gy or 1 x 26 Gy (p = 0.038). The overall survival rate after 1 and 2 years was 52% and 32%, respectively, for lung cancer patients and 85% and 33%, respectively, for metastasis patients, impaired because of systemic disease progression. After 12 months, 60% of patients with primary lung cancer and 35% of patients with pulmonary metastases were without systemic progression. No severe acute or late toxicity was observed, and only 2 patients (3%) developed symptomatic Grade 2 pneumonitis, which was successfully treated with oral steroids.
Stereotactic radiotherapy for lung tumors offers a very effective treatment option locally without significant complications in medically impaired patients who are not amenable to surgery. Patient selection is important, because those with a low risk of systemic progression are more likely to benefit from this approach.
评估采用立体定向放射治疗提高I-II期不可手术的非小细胞肺癌或肺转移患者局部肿瘤控制率的临床效果。
20例I-II期非小细胞肺癌患者和41例有51处肺转移灶且无法手术的患者接受了立体定向放射治疗,照射剂量为3×10 Gy(n = 19)、对包含100%等剂量线的计划靶体积给予3×12 - 12.5 Gy并在等中心归一化至150%(n = 26)或对包含80%等剂量线的计划靶体积给予1×26 Gy(n = 26)。原发性肺癌患者的中位随访时间为11个月(范围2 - 61个月),转移患者的中位随访时间为9个月(范围2 - 37个月)。
治疗后≥1年时,肺癌患者的精算局部控制率为92%,转移患者为80%,将剂量从3×10 Gy增加至3×12 - 12.5 Gy或1×26 Gy可显著提高局部控制率(p = 0.038)。肺癌患者1年和2年的总生存率分别为52%和32%,转移患者分别为85%和33%,因全身疾病进展生存率受到影响。12个月后,60%的原发性肺癌患者和35%的肺转移患者无全身进展。未观察到严重的急性或晚期毒性反应,仅2例患者(3%)出现有症状的2级肺炎,经口服类固醇成功治疗。
对于无法手术且身体状况不佳的患者,立体定向放射治疗肺部肿瘤在局部提供了一种非常有效的治疗选择,且无明显并发症。患者选择很重要,因为全身进展风险低的患者更可能从这种方法中获益。