Impact of next-generation sequencing (NGS) on diagnostic and therapeutic options in soft-tissue and bone sarcoma.

Author:

Gounder Mrinal M.1,Ali Siraj Mahamed2,Robinson Victoria3,Bailey Mark2,Ferraro Richard3,Patel Nirali M3,Krishnan Anita3,Millis Sherri Z.4,Dickson Mark Andrew5,D'Angelo Sandra P.5,Keohan Mary Louise5,Miller Vincent A.2,Schwartz Gary K.6,Maki Robert G.7,Tap William D.5

Affiliation:

1. Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY;

2. Foundation Medicine, Inc., Cambridge, MA;

3. Memorial Sloan-Kettering Cancer Center, New York, NY;

4. Foundation Medicine, Inc., Phoenix, AZ;

5. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY;

6. Columbia University Medical Center, New York, NY;

7. Monter Cancer Center, Northwell Health and Cold Spring Harbor Laboratory, Lake Success, NY;

Abstract

11001 Background: The utility of NGS in management of sarcoma pts remains undefined. Methods: We retrospectively analyzed the NGS profile of patients who were sequenced using a panel of 405 cancer-related genes in DNA and 265 genes rearranged in RNA. Diagnostic and therapeutic implications of mutations (mut) were evaluated through published literature (OncoKb.org, Pubmed). An algorithm was applied to determine germline mut. Following IRB approval, we evaluated the clinical outcomes of pts who underwent NGS at MSKCC. Results: From 2012–2016, 5635 pts worldwide with 56 histologies were tested. Median age of 52 yrs ( < 1-88), 52% females and sarcoma NOS (n = 858) was most frequent. Tumors were sequenced to a mean coverage of 634X; 1165 fusions and > 60,000 mut were found. Mut suspicious for germline defects were seen in 542 pts (9.6%) in known and novel genes ( BRCA, ARID1, FANC). Tumor mutational burden was 2.5/Mb (0–329) and glomus tumors and EHE had the highest and lowest mut, respectively. 16% and 7% of pts had treatment-linked alterations (TLA) known to respond to an FDA approved or study drug, respectively. 42% of pts had TLA eligible for NCI-MATCH, ASCO-TAPUR or other studies. Novel TLA include AKT, ESR1, BRCA, NTRK, PTCH1, SMARCB1 and others. Of the 107 MSKCC pts with clinical data, 60/107 (57%) had at least one TLA, of which 31 (30%) enrolled on a matched trial and 26 pts were ineligible or lacked access to trials. Partial/complete responses were seen with inhibitors to NTRK, IDH1, BRAF, PI3K/mTOR, MDM2, SMARCB1 and others. NGS changed the initial pathology diagnosis and treatments in 5% pts (e.g. LMS to liposarcoma, clear cell to melanoma). Resistance mutations averted futile therapies in 5% pts (e.g. Rb loss and palbociclib in liposarcoma). Conclusions: Our data suggests that NGS has a significant impact in aiding diagnosis and selecting matched therapies in sarcoma. Suspected germline aberrations, while intriguing, needs further validation.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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