Historically, patients with metastatic disease may undergo palliative low-dose radiotherapy for bleeding, pain, or other symptom control from localized progression of disease. However, the advent of increasingly effective systemic therapies has led to interest in exploring how consolidative high-dose locoregional therapies can prolong beneficial effects from systemic therapy in metastatic disease. Investigators have explored local therapy directed at metastatic foci in addition to treatment of in situ primary tumors. In oligometastatic cancers, for patients who did not progress with systemic therapy, the addition of local therapy directed at metastasis has demonstrated an improvement to overall survival (OS) compared with systemic therapy alone in early randomized studies. 1,2 In low-volume metastatic prostate cancer, the addition of primary-directed radiotherapy has also improved OS. 3 Prior retrospective series have demonstrated that patients with metastatic nasopharyngeal cancer (NPC) who receive radiotherapy to their primary and nodal disease have superior outcomes than those who receive systemic therapy alone, and that higher doses of radiotherapy may be associated with superior outcome. 4,5 In an analysis of 718 patients with metastatic NPC in the national cancer database, the 437 patients who received RT had an improved 5-year OS of 28% compared with 10% for those who did not. 4 A review of 105 patients treated at a single institution with metastatic NPC revealed higher doses of radiotherapy (>65 Gy) delivered to the primary site were associated with improved outcomes. 5 Although, to our knowledge, no level I evidence exists to date, based on the aforementioned data and other similar series, the National Comprehensive Cancer Network offers chemoradiotherapy to the primary disease in the head and neck as one of the possible treatment paradigms for metastatic NPC. 6 In this issue of JAMA Oncology, You et al 6 report results from a multicenter randomized clinical trial of patients with metastatic NPC to directly address the benefit of chemoradiotherapy to the primary tumor and nodal disease in this setting. Following the studies in oligometastatic cancer, patients who had a partial response or complete response to 3 cycles of cisplatin and fluorouracil were eligible to be randomized to an additional 3 cycles of chemotherapy alone, or radiotherapy to 70 Gy with concurrent cisplatin/fluorouracil (PF). Of the 173 patients who were assessed for eligibility, 126 had a CR or PR after 3 cycles of chemotherapy and were randomized. The 2-year OS improved by an absolute difference of more than 20%, from 76.4% in the radiotherapy arm vs 54.5% in the chemotherapy-alone group, which led to a hazard ratio of 0.42 for death (P = .004). Not surprisingly, there was a significant decrease in patients who had local or regional recurrence as part of their first recurrence from 70% in the chemotherapy-