Abstract 3630: Validation of the Archer FusionPlex solid tumor panel in the JAX cancer treatment profile TM

Samantha Helm , Aleksandra Ras , Vanessa Spotlow , Kevin Kelly , Susan Mockus , Cara Statz , Guruprasad Ananda , Joan Malcolm , Gregory J. Tsongalis; Abstract 3630: Validation of the Archer FusionPlex solid tumor panel in the JAX cancer treatment profile TM . Cancer Res 15 July 2016; 76 (14_Supplement): 3630. https://doi.org/10.1158/1538-7445.AM2016-3630

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Abstract

Introduction: A comprehensive somatic tumor profile with associated treatment selection options requires the detection of gene fusions. After evaluating the clinical utility of multiple methods of gene fusion detection, it was determined that the Archer FusionPlex Solid Tumor Panel (AFPSTP) best compliments the JAX Cancer Treatment Profile TM (JAX-CTP TM ) clinical test in terms of workflow, specimen requirements and turnaround time. Here we describe our analytical validation process for the AFPSTP assay.

Methods: AFPSTP was validated using 24 samples: 5 JAX Patient Derived Xenograft (PDX) cases, 4 translocation positive controls, 2 FFPE cancer samples, 1 normal tissue sample, and 12 cell lines. Nine of the cell lines were previously identified as positive for fusion transcripts and 3 lacked detectable fusion events. The validation was executed in 5 phases: (1) confirm that AFPSTP was able to detect known fusion or lack of fusion events in characterized specimens; (2) determine inter-assay concordance; (3) determine intra-assay concordance; (4) LOD and (5) sensitivity.

Results: The fusion detection results for this validation are listed in Table 1. All but one of these fusion events was previously identified. The one novel fusion was confirmed using TaqMan RT-PCR. In addition to the expected fusions, 4 false positive events were detected, 2 due to mispriming and 2 determined to be WT read through transcripts. The fusion detection inter and intra-assay concordance was found to be 100% and the sensitivity was calculated to be 91.67% at a LOD of 5%.

Conclusion: This analysis outlines the clinical validation of the incorporation of AFPSTP into the JAX-CTP TM test system. Once incorporated, the AFPSTP assay will accomplish the goal of making JAX-CTP TM a more comprehensive somatic tumor profiling assay without affecting the current acceptable turnaround time or required input material.

List of 15 samples that were found to be fusion positive and the corresponding detected fusion.

HorizonDx EML4/ALK Positive EML4 → ALK variant 1
HorizonDx RET Positive CCDC6 → RET
HorizonDx ROS Positive SLC34A2 → ROS1
HorizonDx Triple Positive EML4 → ALK variant 3b
HorizonDx Triple Positive SLC34A2 → ROS1
HorizonDx Triple Positive CCDC6 → RET
A673 Cell Line EWSR1 → FLI1
VCaP Cell Line TMPRSS2 → ERG
KM-12 Cell Line TPM3 → NTRK1
RPMI-2650 Cell Line BRD4 → NUTM1
NCI-H716 Cell Line FGFR2 → COL14A1
OCI-AML2 Cell Line MBNL1 → RAF1
REH Cell Line ETV6 → RUNX1
MDA-MB-175-VII Cell Line TENM4 → NRG1
ASPS-1 Cell Line TFE3 → ASPSCR1
ASPS-1 Cell Line ASPSCR1 → TFE3
PDX1 EML4 → ALK 3b
PDX2 SYN2 → PPARG
HorizonDx EML4/ALK Positive EML4 → ALK variant 1
HorizonDx RET Positive CCDC6 → RET
HorizonDx ROS Positive SLC34A2 → ROS1
HorizonDx Triple Positive EML4 → ALK variant 3b
HorizonDx Triple Positive SLC34A2 → ROS1
HorizonDx Triple Positive CCDC6 → RET
A673 Cell Line EWSR1 → FLI1
VCaP Cell Line TMPRSS2 → ERG
KM-12 Cell Line TPM3 → NTRK1
RPMI-2650 Cell Line BRD4 → NUTM1
NCI-H716 Cell Line FGFR2 → COL14A1
OCI-AML2 Cell Line MBNL1 → RAF1
REH Cell Line ETV6 → RUNX1
MDA-MB-175-VII Cell Line TENM4 → NRG1
ASPS-1 Cell Line TFE3 → ASPSCR1
ASPS-1 Cell Line ASPSCR1 → TFE3
PDX1 EML4 → ALK 3b
PDX2 SYN2 → PPARG

Citation Format: Samantha Helm, Aleksandra Ras, Vanessa Spotlow, Kevin Kelly, Susan Mockus, Cara Statz, Guruprasad Ananda, Joan Malcolm, Gregory J. Tsongalis. Validation of the Archer FusionPlex solid tumor panel in the JAX cancer treatment profile TM . [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 3630.