Li Hongqi, Li Jing, Wang Xuan, Pang Haifeng, Di Yupeng, Ren Gang, Li Ping, Liu Chen, Chen Xiao, Kang Xiaoli, Wang Yingjie, Xia Tingyi
Department of Radiation Oncology, Airforce General Hospital PLA, Beijing, China.
Medical School, People's Liberation Army General Hospital, Beijing, China.
Front Oncol. 2018 Dec 21;8:618. doi: 10.3389/fonc.2018.00618. eCollection 2018.
Stereotactic ablative radiosurgery (SRS) or stereotactic ablative body radiotherapy (SABR) is the standard treatment for patients with inoperable early stage non-small cell lung cancer (NSCLC), the body gamma knife SRS (ɤ-SRS) is a special SABR technology developed in China. This study prospectively assessed the clinical outcome, toxicity and cost following body ɤ-SRS for early stage NSCLC. From 2007 to 2010, a total of 29 patients with early stage NSCLC were prospectively enrolled in this study. The prescription dose for Planning Target Volume (PTV), Clinical Target Volume (CTV), and Gross Target Volume (GTV) were 50, 60, and 70 gray (Gy) in 10 fractions. Isodose curves of 50, 60, and 70% covered at least 100% of PTV, 90% of CTV, and 80% of GTV, respectively. The body ɤ-SRS was delivered 5 days per week and completed in 2 weeks. Median follow-up time was 62.0 (range 11.1-140.3) months. 1-, 3-, 5-year OS rates were 93.1%, 72.0%, 60.3%; PFS rates were 86.2, 64.2 and 48.8%; and LR, RR, and DM rates were 10.9%, 21.4%, 29.0%. The median cost of the body ɤ-SRS during treatment was 4,838 (range 4,615-4,923) dollars and the median cost through 5 years was 36,960 (range 9920-56,824) dollars. With existing clinical data, the body ɤ-SRS is an effective treatment option for patients with medically inoperable early stage NSCLC or patients who do not prefer operation, as they may benefit from the minimized toxicity. Due to excellent cost effectiveness, the availability of the body ɤ-SRS will expand, especially in developing nations, and underdeveloped countries.
立体定向消融放射外科治疗(SRS)或立体定向消融体部放射治疗(SABR)是无法手术的早期非小细胞肺癌(NSCLC)患者的标准治疗方法,体部伽玛刀SRS(ɤ-SRS)是我国研发的一种特殊SABR技术。本研究前瞻性评估了体部ɤ-SRS治疗早期NSCLC后的临床疗效、毒性和成本。2007年至2010年,共有29例早期NSCLC患者前瞻性纳入本研究。计划靶体积(PTV)、临床靶体积(CTV)和大体靶体积(GTV)的处方剂量分别为50、60和70格雷(Gy),分10次给予。50%、60%和70%的等剂量曲线分别至少覆盖PTV的100%、CTV的90%和GTV的80%。体部ɤ-SRS每周治疗5天,2周内完成。中位随访时间为62.0(范围11.1-140.3)个月。1年、3年、5年总生存率分别为93.1%、72.0%、60.3%;无进展生存率分别为86.2%、64.2%和48.8%;局部复发、区域复发和远处转移率分别为10.9%、21.4%、29.0%。体部ɤ-SRS治疗期间的中位成本为4838(范围4615-4923)美元,5年的中位成本为36960(范围9920-56824)美元。根据现有临床数据,体部ɤ-SRS对于医学上无法手术的早期NSCLC患者或不倾向于手术的患者是一种有效的治疗选择,因为他们可能从最小化的毒性中获益。由于具有出色的成本效益,体部ɤ-SRS的可及性将会扩大,尤其是在发展中国家和欠发达国家。