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First-Line Radiotherapy for Colorectal Cancer Liver Metastases
Selective internal radiotherapy with yttrium-90 resin microspheres (SIRT) has proven beneficial as a third-line or subsequent therapy for patients with colorectal cancer (CRC) liver metastases. To determine the potential benefit of adding SIRT to first-line chemotherapy in this setting, investigators conducted a planned pooled analysis of three industry-sponsored, multicenter, open-label, randomized trials involving more than 1100 patients with liver-predominant metastatic CRC.
Most patients were male (66%) and had colon primaries (71%–76%), synchronous metastases (87%), primary tumors in place (50%–55%), and 25% or less liver involvement (68%–69%); a minority had extra hepatic metastases (35%–36%). Patients received first-line FOLFOX chemotherapy with permissible addition of bevacizumab or anti-EGFR therapy versus chemotherapy sequenced with two intrahepatic infusions of SIRT given during the first two cycles of chemotherapy.
At a median follow-up of 43.3 months, median overall survival was similar with chemotherapy plus SIRT versus chemotherapy alone for all patients (22.6 and 23.3 months, respectively), as well as for those with liver-only metastases (24.5 and 24.6 months). The response rate was higher with SIRT (72% vs. 63%; P=0.0012), as was the rate of response in the liver. However, grade 3 or higher adverse events were more likely with SIRT (odds ratio, 1.42; P=0.0089).
Comment
The use of SIRT with first-line chemotherapy for metastatic CRC failed to improve survival and increased the risk for serious adverse events. This therapy should not be used in first-line treatment of metastatic CRC with liver-confined or liver-predominant disease.
Citation(s)
Author:
Wasan HS et al.
Title:
First-line selective internal radiotherapy plus chemotherapy versus chemotherapy alone in patients with liver metastases from colorectal cancer (FOXFIRE, SIRFLOX, and FOXFIRE-Global): A combined analysis of three multicentre, randomised, phase 3 trials.
Source:
Lancet Oncol
2017
Sep
; [e-pub].
(Abstract/FREE Full Text)
Empfohlen von
David H. Ilson, MD, PhD