Prospective evaluation of quantitative response parameter in patients with Gastrointestinal Stroma Tumor undergoing tyrosine kinase inhibitor therapy—Impact on clinical outcome

Author:

Meyer Mathias123ORCID,Ota Hideki4,Messiou Christina5,Benson Charlotte6,Henzler Thomas1,Mattonen Sarah A.7,Marin Daniele2,Bartsch Anna18,Schoenberg Stefan O.1,Riedel Richard F.9,Hohenberger Peter10

Affiliation:

1. Department of Radiology and Nuclear Medicine University Medical Center Mannheim, Medical Faculty Mannheim—Heidelberg University Mannheim Germany

2. Department of Radiology Duke University Medical Center Durham North Carolina USA

3. Department of Diagnostic and Interventional Radiology and Nuclear Medicine University Hospital Hamburg‐Eppendorf Hamburg Germany

4. Department of Diagnostic Radiology Tohoku University Hospital Miyagi Japan

5. Department of Radiology Royal Marsden Hospital and Institute of Cancer Research London UK

6. The Royal Marsden Hospital NHS Foundation Trust London UK

7. Department of Medical Biophysics Western University London Canada

8. Department of Orthopedics and Traumatology University Hospital Basel Basel Switzerland

9. Duke Cancer Institute Duke University Medical Center Durham North Carolina USA

10. Division of Surgical Oncology and Thoracic Surgery University Medical Center Mannheim, Ruprecht‐Karl University of Heidelberg Mannheim Germany

Abstract

AbstractThe purpose of this study was to determine if dual‐energy CT (DECT) vital iodine tumor burden (ViTB), a direct assessment of tumor vascularity, allows reliable response assessment in patients with GIST compared to established CT criteria such as RECIST1.1 and modified Choi (mChoi). From 03/2014 to 12/2019, 138 patients (64 years [32–94 years]) with biopsy proven GIST were entered in this prospective, multi‐center trial. All patients were treated with tyrosine kinase inhibitors (TKI) and underwent pre‐treatment and follow‐up DECT examinations for a minimum of 24 months. Response assessment was performed according to RECIST1.1, mChoi, vascular tumor burden (VTB) and DECT ViTB. A change in therapy management could be because of imaging (RECIST1.1 or mChoi) and/or clinical progression. The DECT ViTB criteria had the highest discrimination ability for progression‐free survival (PFS) of all criteria in both first line and second line and thereafter treatment, and was significantly superior to RECIST1.1 and mChoi (p < .034). Both, the mChoi and DECT ViTB criteria demonstrated a significantly early median time‐to‐progression (both delta 2.5 months; both p < .036). Multivariable analysis revealed 6 variables associated with shorter overall survival: secondary mutation (HR = 4.62), polymetastatic disease (HR = 3.02), metastatic second line and thereafter treatment (HR = 2.33), shorter PFS determined by the DECT ViTB criteria (HR = 1.72), multiple organ metastases (HR = 1.51) and lower age (HR = 1.04). DECT ViTB is a reliable response criteria and provides additional value for assessing TKI treatment in GIST patients. A significant superior response discrimination ability for median PFS was observed, including non‐responders at first follow‐up and patients developing resistance while on therapy.

Funder

Siemens Healthineers

Novartis Pharma

Publisher

Wiley

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