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. 2022 Jan 30;14(3):718. doi: 10.3390/cancers14030718

Table 1.

Selected trials of oligoprogressive NSCLC patients treated with local ablative therapies combined with TKI.

Author (Year) Type of Study N. of Patients Molecular Status LAT Sites mPFS (Months) mOS (Months)
Weickhardt et al.
(2012) [9]
Retrospective 25 EGFR+, ALK+ (54%) SBRT, SRS, WBRT, XRT, surgery CNS + eCNS 6.2 * -
Gan et al.
(2014) [22]
Retrospective 14 ALK+ (100%) SBRT, HRT, surgery eCNS 5.5 * 39
Liu et al.
(2018) [23]
Retrospective 38 ALK+ (86.8%), ROS1+ SBRT, WBRT CNS + eCNS 9.9 * -
Kroeze et al.
(2021) [24]
Retrospective 108 EGFR+, ALK+ (15%), ROS1+, WT SRS, SBRT CNS + eCNS 10.4 -
Borghetti P et al.
(2019) [25]
Retrospective 106 EGFR+, ALK+ (19%) SRT, HRT CNS + eCNS - 23
Ni et al.
(2019) [26]
Retrospective 19 ALK+ (100%) SBRT, SRS, WBRT CNS + eCNS 10 * -
Takeda et al.
(2013) [27]
Retrospective 7 ALK+ (100%) WBRT, SRS CNS 5.5 * -

LAT: local ablative therapy; mPFS: median progression-free survival; mOS: median overall survival; TKI: tyrosine kinase inhibitor; HRT: hypofractionated radiotherapy; SBRT: stereotactic body radiation therapy; SRS: stereotactic radiosurgery; XRT: standard radiation therapy; SRT: stereotactic radiotherapy; WT: wild-type; CNS: central nervous system; eCNS: extra-CNS. * Calculated from progression on TKI. The Kroesze et al. study included both oligoprogressive (≤5 metastatic sites) and polyprogressive (>5 metastatic sites) patients. In oligoprogressive patients (56%) mPFS was 10.4 months. The Ni et al. study included both oligoprogressive/oligometastatic (≤4 metastatic sites) and polyprogressive (>5 metastatic sites) patients. Fifty-two patients were defined as oligometastatic/oligoprogressive. SRT with an ablative intent was administered in 49 patients.