Treatment of bulky uveal melanoma (UN) hepatic metastases with doxorubicin eluting beads (DEBDOX) followed by 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) TACE: an initial experience

2014 ◽  
Vol 25 (3) ◽  
pp. S45
Author(s):  
A.L. Tan ◽  
D.J. Eschelman ◽  
C.F. Gonsalves ◽  
A. Frangos ◽  
T. Sato
2012 ◽  
Vol 97 (2) ◽  
pp. 159-163 ◽  
Author(s):  
Ernie Marshall ◽  
Christopher Romaniuk ◽  
Paula Ghaneh ◽  
Helen Wong ◽  
Marie McKay ◽  
...  

HPB ◽  
2020 ◽  
Vol 22 (4) ◽  
pp. 497-505 ◽  
Author(s):  
Alistair Rowcroft ◽  
Benjamin P.T. Loveday ◽  
Benjamin N.J. Thomson ◽  
Simon Banting ◽  
Brett Knowles

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. 10025-10025 ◽  
Author(s):  
David R. Minor ◽  
Takami Sato ◽  
Marlana M. Orloff ◽  
Jason J. Luke ◽  
David J. Eschelman ◽  
...  

10025 Background: Hepatic metastases from uveal melanoma have no established therapy, with a median survival of only 6-12 months. To date therapy with checkpoint inhibitors has yielded minimal results. To take advantage of possible synergy between radiation and immunotherapy we treated patients with yttrium90 internal radiation followed by immunotherapy. Methods: Patients received yttrium90 (Sir-Spheres) via hepatic artery infusion in two treatments, one to each lobe 3-4 weeks apart, followed in 3-6 weeks by ipilimumab and nivolumab for 4 doses, then nivolumab maintenance. Results: We are presenting interim results because of the excessive toxicity seen when these FDA-approved modalities were used in sequence with the FDA-approved dosages. Initially dosing of yttrium90 (Y90) followed the package insert “BSA method” but after 8 patients we had 5 cases of grade 3-4 hepatic toxicity; in 4 cases the toxicity was observed after just the Y90. One case of cirrhosis occurred in a patient whose liver received 40-45Gy; her cirrhosis was felt most likely due to the Y90. Y90 dosing was then reduced to limit dosage to normal liver to 35Gy, and none of the next 5 patients have had more than grade 2 hepatic toxicity. Dosage to the normal liver is approximated by the MIRD formula: Actual delivered liver dose [Gy] = 50 * Administered activity [GBq] * (1 – Lung shunt fraction) / kg of treated liver. If calculated dose was > 35GY, dosage in GBq is reduced proportionally. Toxicity in the first 5 patients to receive immunotherapy included one grade 4, two grade 3 and two grade 2 hepatic toxicities, and only 3 of the 5 patients received more than one dose of ipilimumab. We then reduced dosing of ipilimumab from 3mg/kg x 4 to 1mg/kg x 4 because of this excessive autoimmune toxicity. Of 13 patients, 10 received both Y90 and immunotherapy, and 3 had responses (1 CR, 2 PR) with 3 patients stable > 5months. Median progression-free survival for all patients is 27 weeks and median overall survival is greater than 48 weeks. Treatment with Y90 produced an over 50% fall in peripheral blood lymphocytes which was reversed in most patients by the immunotherapy. Conclusions: With dose modifications this therapy appears feasible and objective tumor responses were seen. Sequential therapy with Y90 and immunotherapy appears tolerable if radiation to normal liver is limited to 35Gy and ipilimumab dose is 1mg/kg. Clinical trial information: NCT02913417.


2012 ◽  
Vol 199 (6) ◽  
pp. 1387-1392 ◽  
Author(s):  
Gundula Edelhauser ◽  
Nikolaus Schicher ◽  
Dominik Berzaczy ◽  
Dietrich Beitzke ◽  
Christoph Höeller ◽  
...  

2004 ◽  
Vol 21 (4) ◽  
pp. 314-320 ◽  
Author(s):  
T.J. White ◽  
S.H. Roy-Choudhury ◽  
D.J. Breen ◽  
J. Cast ◽  
A. Maraveyas ◽  
...  

2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e21018-e21018
Author(s):  
Giovanna Campiolo ◽  
Milton Jose De Barros E. Silva ◽  
Mariana Petaccia de Macedo ◽  
Jose Augusto Rinck

e21018 Background: Uveal melanoma is the most common primary ocular tumor in adults and accounts for 5% of all melanoma diagnoses in the United States. Approximately fifty percent of patients with uveal melanoma develop metastatic disease. The most frequent site of metastasis from UM is the liver (89 to 95% of the cases) and liver failure is the leading cause of death. To date, no systemic therapy has shown benefits in terms of overall survival (OS) in UM. Methods: We retrospectively analyzed clinical characteristics and aspects of response to systemic and local therapy of a cohort of 58 patients with UM who were treated in our institution from January of 2000 to December of 2017. Survival curves were calculated by Kaplan-Meier method and log-rank test. Results: Median age was 55y. 64% of the patients were female and 48,3% of them were caucasian. With a median follow-up time of 23 months, the median OS was 28,4 months. The median time between primary treatment and systemic relapse was 3.7 years. In 90% of the cases the liver was the unique site of progression. 12% patients had liver metastasectomy as local treatment, with OS of 102,3 months vs. 24,5 months ( p= 0,04) for no local treatment. 12% of the patients with liver methastasis perfomed regional treatment with intra-arterial chemotherapy (IAC) and 17% with chemoembolization (CE). The progression free survival (PFS) for regional treatment was 2.9 months (0,9-27 m); 4,25 months (0,9-27 m) for IAC and 2,9 months (0,9-27 m) for CE. There was no significant benefit in OS for locorregional treatment. As first line treatment, 29% of patients had chemotherapy, 10% had ipilimumab and 3,4% had anti-PD1. The median PFS for first line treatment was 2,49 months; 2 months for chemotherapy, 3,8 months for ipilimumab and 14 months for anti-PD1. The median PFS for second line treatment was 2,8 months and for third line was 2,3 months. There was no consistent clinical impact in OS for systemic treatment. Conclusions: The current systemic treatments available for cutaneous melanoma have limited efficacy in UM, so far none have yet proven a survival benefit. Locorregional therapies are relevant for patients with unresectable hepatic metastases. Resection of liver lesions in highly selected cases has the potential to improve patient outcomes, but the survival advantage may partially reflect patient selection.


2019 ◽  
Author(s):  
Mizue Terai ◽  
Emma Link ◽  
Carin F. Gonsalves ◽  
David J. Eschelman ◽  
Rober D. Adamo ◽  
...  

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