Sequential intra-arterial infusion of 90Y-resin microspheres and mitomycin C in chemo refractory liver metastatic breast cancer patients: a single centre pilot study

Author:

Aarts Brigitte Maximiliana12,Klompenhouwer Elisabeth Geneviève1,Dresen Raphaëla Carmen3,Deroose Christophe Michel Albert Louis Omer4,Beets-Tan Regina Gien Hoa12,Punie Kevin5,Neven Patrick5,Wildiers Hans5,Maleux Geert3

Affiliation:

1. Radiology, The Netherlands Cancer Institute , Amsterdam , The Netherlands

2. GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre , Maastricht , The Netherlands

3. Radiology, University Hospitals Leuven , Leuven , Belgium

4. Nuclear Medicine, University Hospitals Leuven , Leuven , Belgium

5. General Medical Oncology, University Hospitals Leuven , Leuven , Belgium

Abstract

Abstract Background The aim of the study was to evaluate the safety and feasibility of intra-arterial mitomycin C (MMC) infusion after selective internal radiation therapy (SIRT) using Yttrium-90 (90Y) resin microspheres in liver metastatic breast cancer (LMBC) patients. Patients and methods The prospective pilot study included LMBC patients from 2012–2018. Patients first received infusion of 90Y resin microspheres, after 6–8 weeks response to treatment was assessed by MRI, 18F-FDG PET/CT and laboratory tests. After exclusion of progressive disease, MMC infusion was administrated 8 weeks later in different dose cohorts; A: 6 mg in 1 cycle, B: 12 mg in 2 cycles, C: 24 mg in 2 cycles and D: maximum of 72 mg in 6 cycles. In cohort D the response was evaluated after every 2 cycles and continued after exclusion of progressive disease. Adverse events (AE) were reported according to CTCAE version 5.0. Results Sixteen patients received 90Y treatment. Four patients were excluded for MMC infusion, because of extra hepatic disease progression (n = 3) and clinical and biochemical instability (n = 1). That resulted in the following number of patient per cohort; A: 2, B: 1, C: 3 and D: 6. In 4 of the 12 patients (all cohort D) the maximum dose of MMC was adjusted due biochemical toxicities (n = 2) and progressive disease (n = 2). One grade 3 AE occurred after 90Y treatment consisting of a gastrointestinal ulcer whereby prolonged hospitalization was needed. Conclusions Sequential treatment of intra-arterial infusion of MMC after 90Y SIRT was feasible in 75% of the patients when MMC was administrated in different escalating dose cohorts. However, caution is needed to prevent reflux after 90Y SIRT in LMBC patients.

Publisher

Walter de Gruyter GmbH

Subject

Radiology Nuclear Medicine and imaging,Oncology

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