Reported time [Ref.] | MET fusion types | Primary/ acquired | Stage | EGFR/ALK mutations | Pathological types | The PFS of crizotinib treatment and best overall response |
---|---|---|---|---|---|---|
2017 [14] | KIF5B-MET | Primary | IV | WT | LUAD | 10.0Â months, PR |
2017[18] | HLA-DRB1-MET | Primary | IV | WT | LUAD | 8.0Â months, complete resolution of lung nodules |
2018 [18] | KIF5B-MET | Primary | IV | WT | LUAD | 8.0Â months, PR |
2018 [18] | STARD3NL-MET | Primary | IV | WT | LUAD | 14.0Â months, PR |
2018 [18] | MET-ATXN7L1 | Primary | IV | WT | LUAD | 4Â months, PR |
2018[18] | MET-UBE2H | Acquired | IV | EGFR exon 19 deletion | LUAD | 6.5Â months, PR |
2019 [15] | CAV1-MET | Acquired | IV | EGFR exon 21 L858R | LUAD, SCLC transformation | NR (plus osimertinib), PR |
2020 [19] | HLA-DRB1-MET | Primary | IV | WT | LUAD | 7.0Â months, complete resolution of lung/brain nodules |
2021[18] | HLA-DRB1-MET | Primary | IV | WT | LUAD | NR, CR |
2022 [16] | ARL1-MET | Primary | IV | WT | LUAD | 5.0Â months, PR |
2022 [17] | CUX1-MET | Acquired | IV | EGFR exon 18 G719D and exon 21 L861Q | LUAD | 9.0Â months(plus icotinib), PR |
2022 [20] | MET-DSTN | Acquired | IV | EGFR exon 21 L858R | LUAD | NR (plus gefitinib), CR |