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Clinical Trial
. 2024 Aug;31(8):5340-5351.
doi: 10.1245/s10434-024-15293-x. Epub 2024 May 4.

Efficacy and Safety of the Melphalan/Hepatic Delivery System in Patients with Unresectable Metastatic Uveal Melanoma: Results from an Open-Label, Single-Arm, Multicenter Phase 3 Study

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Clinical Trial

Efficacy and Safety of the Melphalan/Hepatic Delivery System in Patients with Unresectable Metastatic Uveal Melanoma: Results from an Open-Label, Single-Arm, Multicenter Phase 3 Study

Jonathan S Zager et al. Ann Surg Oncol. 2024 Aug.

Erratum in

Abstract

Background: Uveal melanoma (UM) has a poor prognosis once liver metastases occur. The melphalan/Hepatic Delivery System (melphalan/HDS) is a drug/device combination used for liver-directed treatment of metastatic UM (mUM) patients. The purpose of the FOCUS study was to assess the efficacy and safety of melphalan/HDS in patients with unresectable mUM.

Methods: Eligible patients with mUM received treatment with melphalan (3.0 mg/kg ideal body weight) once every 6 to 8 weeks for a maximum of six cycles. The primary end point was the objective response rate (ORR). The secondary end points included duration of response (DOR), overall survival (OS), and progression-free survival (PFS).

Results: The study enrolled 102 patients with mUM. Treatment was attempted in 95 patients, and 91 patients received treatment. In the treated population (n = 91), the ORR was 36.3 % (95 % confidence interval [CI], 26.44-47.01), including 7.7 % of patients with a complete response. Thus, the study met its primary end point because the lower bound of the 95 % CI for ORR exceeded the upper bound (8.3 %) from the benchmark meta-analysis. The median DOR was 14 months, and the median OS was 20.5 months, with an OS of 80 % at 1 year. The median PFS was 9 months, with a PFS of 65 % at 6 months. The most common serious treatment-emergent adverse events were thrombocytopenia (15.8 %) and neutropenia (10.5 %), treated mostly on an outpatient basis with observation. No treatment-related deaths were observed.

Conclusion: Treatment with melphalan/HDS provides a clinically meaningful response rate and demonstrates a favorable benefit-risk profile in patients with unresectable mUM (study funded by Delcath; ClinicalTrials.gov identifier: NCT02678572; EudraCT no. 2015-000417-44).

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Figures

Fig. 1
Fig. 1
Kaplan-Meier plots of a progression-free survival and b overall survival in patients treated with melphalan/Hepatic Delivery System (HDS) (treated population: assessed by Independent Review Committee)
Fig. 2
Fig. 2
Post hoc analysis. a Kaplan-Meier plot of overall survival by best overall response. b Overall survival by best overall response and c first occurrence of objective response by treatment cycle in patients treated with the melphalan/Hepatic Delivery System (treated population, assessed by Independent Review Committee). CI, confidence interval; CR, complete response; NC, not calculable; ND, not defined; OS, overall survival; PD, progressive disease; PR, partial response; SD, stable disease

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