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Precision Oncology in Solid Tumors: A Longitudinal Tertiary Care Center Experience.

Authors :
Sadaps, Meena
Funchain, Pauline
Mahdi, Haider
Grivas, Petros
Pritchard, Amy
Klek, Stefan
Estfan, Bassam
Abraham, Jame
Budd, G. Thomas
Stevenson, James P.
Pennell, Nathan A.
Khorana, Alok A.
Bolwell, Brian J.
Sohal, Davendra P.S.
Source :
JCO Precision Oncology. 11/27/2018, Vol. 2, p1-11. 11p.
Publication Year :
2018

Abstract

Purpose: Precision oncology is widely discussed, but cohort studies are limited. We previously reported our prospective experience of precision oncology in solid tumors, and here we report our longitudinal experience, focusing on therapeutic impact. Patients and Methods: We conducted a retrospective review of 600 consecutive patients seen at Cleveland Clinic from 2013 to 2016 for treatment of incurable solid tumor malignancies for whom tumor genomic profiling was ordered using FoundationOne (Cambridge, MA). Results were discussed at our multidisciplinary genomics tumor board. Data analyzed included subsequent therapy and overall survival (OS). Results: Median age was 59 years (range, 18 to 94 years), 308 (51.3%) were female, and 533 (88.8%) were white. Targeted therapy was recommended in 310 patients (51.7%). After results, 313 patients (52.2%) started any subsequent therapy; of these, 95 (30%; 15.8% overall) received genomics-driven therapy (G), and 218 (70%) received non–genomics-driven treatment (NG). For the G versus NG group, the on-label, off-label, and clinical trial therapy breakdowns were 23% versus 88%, 47% versus 3%, and 30% versus 9%, respectively. Median OS for patients receiving no therapy after tumor genomic profiling was 5.5 months; for the G and NG groups, it was 18 (P <.001) and 14.4 (P <.001) months, respectively (P = NS for G v NG). The use of G increased from 10% in the first 250-patient cohort (reported earlier) to 20% in the subsequent 350-patient cohort. Conclusion: Tumor genomic profiling influenced treatment in 15.8% of patients. More patients received treatment via clinical trials in the G cohort, and although not statistically significant, there was a trend toward increased OS in the G (v NG) group. These data can further guide real-world applications of precision oncology. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
24734284
Volume :
2
Database :
Academic Search Index
Journal :
JCO Precision Oncology
Publication Type :
Academic Journal
Accession number :
133238097
Full Text :
https://doi.org/10.1200/PO.18.00186