AI Article Synopsis

  • The liver is the main site for metastases in uveal melanoma, prompting the need for targeted treatment methods like transarterial chemoembolization (TACE).
  • Between 2003 and 2008, 25 patients who had liver metastases after systemic therapy were treated with TACE using fotemustine or cisplatin, showing mostly manageable side effects.
  • The treatment resulted in 56% of patients having stable disease for over 2 months, with a median progression-free survival of 3 months and overall survival of 6 months, indicating that TACE could be beneficial, especially for patients with lower lactate dehydrogenase levels.

Article Abstract

The liver is the predominant site of metastases in the majority of patients with uveal melanoma, suggesting the evaluation of regional treatment approaches. Here we report our experience with transarterial chemoembolization (TACE) in uveal melanoma patients with pretreated liver metastases. Twenty-five patients were treated with fotemustine-based or cisplatin-based TACE after treatment failure of systemic therapy between 2003 and 2008 at our institution. Grade III toxicity consisted of gastric ulcer (n=1), fever (n=3), splenic infarction (n=1), and thrombocytopenia (n=1). No grade IV toxicity or catheter-associated complications were observed. Fourteen of 25 patients (56%) had stable disease for at least 2 months and four had partial remission. The median progression-free survival (PFS) was 3 months (95% confidence interval: 2-4 months) and the median overall survival (OS) was 6 months (95% confidence interval: 5-7 months), with 15% of patients alive at 1 year. Both PFS and OS were significantly longer, when pretreatment lactate dehydrogenase was below the two-fold upper limit of normal (n=11): PFS 5 versus 2 months (P<0.001) and OS 11 versus 5 months (P=0.012). All patients with lactate dehydrogenase less than 2xupper limit of normal had a clinically detectable benefit. TACE is well tolerated and effective in pretreated patients with liver metastases from uveal melanoma. TACE should further be evaluated as first-line therapy in prospective randomized clinical trials.

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http://dx.doi.org/10.1097/CMR.0b013e328334c36eDOI Listing

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