Cancer Research and Treatment· 2026Q1
Çağdaş Sistemik Tedaviler Döneminde Akciğer Oligometastazları İçin Ablatif SABR: Etkinlik, Güvenlik ve Optimal Sıralama
Ablative SABR for Pulmonary Oligometastases in the Era of Contemporary Systemic Therapies: Efficacy, Safety, and Optimal Sequencing
- 0atıf
- Q1SCImago
- 2026yıl
Kısa özet
Stereotaktik ablatif radyoterapi (SABR), akciğer metastazlarında %96,2'lik 1 yıllık lokal kontrol sağladı; sonuçlar primer kanser bölgesi, hastalık durumu ve önceki kemoterapi ile etkilendi.
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Özet (abstract)
PurposeThis study evaluated the efficacy and safety of stereotactic ablative radiotherapy (SABR) for pulmonary metastases in the era of contemporary systemic therapy and identified predictors of clinical outcomes and toxicity. Materials and MethodsWe retrospectively analyzed 221 patients with 283 lung metastases from non-pulmonary primary cancers who underwent SABR between 2016 and 2024, with 98.2% of lesions treated to a biologically effective dose (BED10) of ≥100 GyE.Local control (LC), progression-free survival (PFS), overall survival (OS), and radiation pneumonitis (RP) were assessed using Cox proportional hazards and logistic regression models. ResultsAt a median follow-up of 23.7 months, the 1-year LC, PFS, and OS were 96.2%, 46.1%, and 89.5%, respectively.On multivariable analysis, primary cancer site (non-colorectal vs. colorectal: Hazard ratio (HR) 2.49, p=0.025), oligometastatic disease status (de novo vs. repeated: HR 3.14, p=0.026), and pre-SABR cytotoxic chemotherapy (HR 0.08, p=0.006) were identified as independent predictors of LC.Symptomatic RP occurred in 17.0% of cases and was significantly associated with SABR to ≥3 lesions (odds ratio [OR] 2.88, p=0.028), higher lung volume that received ≥10 GyE (OR 1.09, p=0.045), and concurrent administration of high-risk systemic agents, including immune checkpoint inhibitors, cytotoxic agents, or targeted agents (OR 4.01, p=0.015). ConclusionSABR with predominantly ablative-dose regimens provides excellent LC for pulmonary metastases, influenced by primary tumor biology, oligometastatic disease status, and pre- A c c e p t e d A r t i c l e CANCER RESEARCH AND TREATMENT (CRT)
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