Prospective phase II trial on ablative stereotactic body radiation therapy (SBRT) for medically inoperable thoracic nodes metastases

被引:2
作者
Franceschini, D. [1 ]
Teriaca, M. A. [1 ]
Mancosu, P. [1 ]
Bertolini, A. [1 ,2 ]
Lo Faro, L. [1 ,2 ]
Spoto, R. [1 ]
Dominici, L. [1 ]
Badalamenti, M. [1 ]
Bellu, L. [1 ,2 ]
Dei, D. [1 ]
La Fauci, F. [1 ]
Franzese, C. [1 ,2 ]
Scorsetti, M. [1 ,2 ]
机构
[1] IRCCS Humanitas Res Hosp, Dept Radiotherapy & Radiosurg, Via Manzoni 56, I-20089 Rozzano Milan, Italy
[2] Humanitas Univ, Dept Biomed Sci, Via Rita Levi Montalcini 4, I-20072 Pieve Emanuele Milan, Italy
关键词
Stereotactic radiotherapy; Ablative dose; Oligometastases; Thoracic nodes metastases; CELL LUNG-CANCER; LYMPH-NODE; EARLY-STAGE; RADIOTHERAPY; TUMORS;
D O I
10.1016/j.radonc.2024.110335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Oligometastases in mediastinal nodes are increasingly prevalent, posing challenges for treatment with stereotactic body radiotherapy (SBRT) due to proximity to organs at risk (OARs). We report the results of a single prospective observational phase II trial on ablative SBRT for medically inoperable thoracic nodes metastases (NCT02970955). Material and methods: Since 2017, patients with < 3 nodal metastases were evaluated by the tumor board and included if deemed inoperable. SBRT was delivered using risk adaptive approach based on number, site and size of metastatic nodes (50 Gy/5fractions, 60 Gy/8fractions, 70 Gy/10 fractions). Planning target volume (PTV) partial underdosage was allowed. The primary end point was local control (LC) at 12 months. Secondary end points were: acute and late toxicities, overall survival (OS), progression free survival (PFS), and time to next systemic therapy (TTNS). Results: Between 03/2017 - 11/2021, 32 patients (41 nodal metastases) were included. NSCLC (13pts), breast (5pts) and colorectal cancer (4pts) were the most represented primary tumour. In 66 % cases, partial PTV undercoverage was necessary. LC at 1 and 2 years was 93.5 % and 82.3 %, respectively. Treatment was welltolerated with no acute or late toxicity >= G3. Median OS was 59.7 months. OS at 1 and 2 years was 96.9 % and 83.8 % respectively. Median PFS was 12.2 months. PFS at 1 and 2 years was 53.1 % and 31.3 %, respectively. Conclusion: This trial supported the feasibility and safety of ablative SBRT for thoracic nodes metastases thanks to risk adaptive approach allowing to delay of new systemic therapies. Larger studies are needed to confirm these observations.
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