Nivolumab and stereotactic radiation therapy for the treatment of patients with Stage IV non-small-cell lung cancer. (17th November 2018)

• Record Type: Journal Article
• Authors: Miyamoto, Shingo; Nomura, Ryutaro; Sato, Kengo; Awano, Nobuyasu; Kuse, Naoyuki; Inomata, Minoru; Izumo, Takehiro; Terada, Yuriko; Furuhata, Yoshiaki; Bae, Yuan; Kunitoh, Hideo
• Is Part Of: Japanese journal of clinical oncology. Volume 49:Number 2(2019)
• Page Start: 160
• Page End: 164
• Publication Date: 2018-11-17
• Subjects: radiosurgery -- nivolumab -- non-smal-cell lung carcinoma; Oncology -- Periodicals; Cancer -- Periodicals; 616.994005
• DOI: 10.1093/jjco/hyy171
• Languages: English
• ISSNs: 0368-2811

Abstract

Abstract : Radiotherapy may function as a powerful initiator for immunotherapy. We performed a study of stereotactic radiation therapy plus nivolumab. This combination therapy was well tolerated. Abstract: Background: Radiation therapy might modify the cancer immune environment to enhance the antitumor effect of immune checkpoint inhibitors. We performed a feasibility study of nivolumab following stereotactic radiation therapy for chemotherapy pretreated advanced non-small-cell lung cancer. Patients and methods: Pretreated advanced/recurrent non-small-cell lung cancer patients received stereotactic radiation therapy to one of the disease sites. Nivolumab at a dose of 3 mg/kg was given within 2 weeks after the completion of stereotactic radiation therapy and continued every 2 weeks thereafter until disease progression or unacceptable toxicities. The primary endpoint was the occurrence rate of Grade 3 pneumonitis (within 12 weeks) or other non-hematological toxicity (within 8 weeks). Results: From September 2016 to September 2017, six patients were enrolled. Five received stereotactic radiation therapy to their primary lesions. All patients received nivolumab on the following day after stereotactic radiation therapy completion. Grade 3 pneumonitis occurred in one patient, but no other serious adverse events were reported for the other patients. One complete response and two partial responses were achieved. Four patients had measurable lesions outside the irradiated area, of whom three patients responded to the treatment. The initial progression sites were mainly outside the irradiated field, including one brain metastasis. Conclusions: Nivolumab therapy immediately following stereotactic radiation therapy was well tolerated. This sequential combination warrants further study.