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Phase I trial of dose-escalated whole liver irradiation with hepatic arterial fluorodeoxyuridine/leucovorin and streptozotocin followed by fluorodeoxyuridine/leucovorin and chemoembolization for patients with neuroendocrine hepatic metastases

American Journal of Clinical Oncology Apr 02, 2018

Shilkrut M, et al. - Researchers have previously demonstrated that moderate doses of chemoradiotherapy can elicit a response in patients with refractory neuroendocrine tumors. In a dose-escalation phase I/II trial combining hepatic arterial (HA) chemotherapy, chemoembolization, and dose-escalated whole liver radiotherapy, they looked for the maximum safe dose of radiation that could be delivered and to make a preliminary assessment of response. It was found safe to deliver thirty-two in 2 Gy daily fractions in combination with HA chemotherapy and subsequent transarterial chemoembolization. Despite objective responses, this combination was not significantly better than the prior approaches.
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