Table 1.
Study | Number of RET-FISH+ Samples Reported | Number of RET-FISH+ Samples Compared With Other Techniques | Number and % of Concordant Samples Between FISH and Other Techniques | Comments |
---|---|---|---|---|
Kim et al.,32 2018 | 51 | 51 | 3 (5.9) [NanoString] | |
Radonic et al.,30 2021 | 48 | 30 | 9 (30) [RNA-seq] | |
Tsuta et al.,27 2014 | 50 | 29 | 16 (55.2) [RT-PCR] | RT-PCR analysis only when RNA was available (29) and 14 KIF5B::RET fusions and 2 CCDC6::RET fusions were confirmed. |
Takeuchi et al.,26 2012 | 22 | 22 | 12 (54.5) [RT-PCR] | |
Tan et al.,29 2020 | 30 | 9 | 6 (66.7) [NGS] | 2 equivocal FISH samples (10-15% positive cells) were also positive by RNA-seq. |
Baker et al.,31 2021 | 8 | 8 | 5 (62.5) [RNA-seq] | |
Go et al.,33 2013 | 3 | 3 | 3 (100) [PCR] 3 (100%) [WTS] |
|
Rogers et al.,28 2017 | 1 | 1 | 0 (0) [NanoString] 1 (100) [Agena] 0 (0) [RNA-seq] |
The only RET-FISH-positive case in this study was also the most degraded sample, failing to be detected by NanoString and ThermoFisher RNA-seq, and was borderline positive with Agena allele-specific assay. |
Piton et al.,34 2018 | 1 | 1 | 1 (100) [ligation-dependent RT-PCR] | FISH-positive cases with rearranged nuclei between 15 and 20% were excluded because it was a high risk of a false-positive result, as the authors did not want to test LD-RT-PCR on these unsure 'positive' cases. |
FISH, fluorescence in situ hybridization; LD-RT-PCR, ligation-dependent reverse transcription polymerase chain reaction; NGS, next generation sequencing; PCR, polymerase chain reaction; RNA-seq, RNA-sequencing; RT-PCR, reverse transcription polymerase chain reaction; WTS, whole transcriptome sequencing.