The use of radiation therapy for oligoprogressive/oligopersistent oncogene-driven non small cell lung cancer: State of the art

被引:28
|
作者
Franceschini, D. [1 ]
De Rose, F. [1 ]
Cozzi, S. [1 ]
Franzese, C. [1 ]
Rossi, S. [2 ]
Finocchiaro, G. [2 ]
Toschi, L. [2 ]
Santoro, A. [2 ,3 ]
Scorsetti, M. [1 ,3 ]
机构
[1] Humanitas Clin & Res Ctr, Radiotherapy & Radiosurg Dept, Milan, Italy
[2] Humanitas Clin & Res Ctr, Dept Oncol & Hematol, Milan, Italy
[3] Humanitas Univ, Dept Biomed Sci, Milan, Italy
关键词
Lung cancer; Oncogene-driven; Oligoprogression; Oligopersistence; Radiotherapy; TYROSINE KINASE INHIBITORS; GROWTH-FACTOR RECEPTOR; LOCAL ABLATIVE THERAPY; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; BRAIN METASTASES; DISEASE-CONTROL; OPEN-LABEL; GEFITINIB; PROGRESSION;
D O I
10.1016/j.critrevonc.2020.102894
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncogene-driven non small cell lung cancer (NSCLC) is a distinct entity in thoracic oncology. The availability of effective target therapies, like EGFR inhibitors or ALK inhibitors, have revolutionized the prognosis of these patients. However, despite an initial response in the majority of patients, drug resistance ultimately occurs. In some cases, this resistance develops in few clonal cells (oligoprogression), so that a local ablation of these resistant deposits could allow to maintain the same systemic therapy and possibly to prolong patients' survival. For these purposes, stereotactic body radiation therapy (SBRT) is an ideal local ablative treatment, because it is effective, non invasive and with limited side effects. In this review, we aim to analyze available clinical data to verify whether SBRT can allow these patients to continue with existing target therapy longer, delay the switch to other systemic therapies and improve their outcome modifying the natural history of the disease.
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页数:7
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