Addition of Low Dose Nivolumab to Salvage Chemotherapy in Patients with Relapsed/Refractory Hodgkin Lymphoma

在复发/难治性霍奇金淋巴瘤患者的挽救性化疗中加入低剂量纳武利尤单抗

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Abstract

INTRODUCTION: Several studies have explored different doses of checkpoint inhibitors in various malignancies, but the optimal dose remains undefined. Here, we present our data on the use of low-dose Nivolumab (LD-Nivo) in combination with conventional chemotherapy for patients with Relapsed/Refractory Hodgkin lymphoma (RRHL). METHODS: All patients with RRHL who received LD-Nivo with conventional chemotherapy between 2020 and 2024 were included in the study. All patients received a fixed dose of 40 mg of Nivolumab per cycle. RESULTS: Twenty-one patients were included in the study with a median age of 26 years. The majority of patients had refractory disease (n = 16; 76.2%). Median Nivolumab dose per cycle was 0.66 mg/kg and median number of cycles of therapy was 3. The overall response rate was 100% with 19 patients achieving a complete response (90.5%). Eleven patients (52.4%) underwent an Autologous hematopoietic cell transplant post salvage therapy. The median follow-up was 23 months during which 2 patients relapsed. There were no deaths during follow-up. Median progression-free and overall survival were not reached. CONCLUSION: The addition of a fixed 40 mg dose of Nivolumab to conventional salvage therapy has demonstrated high response rates and favourable outcomes. This may serve as a viable option in Low/Middle Income Countries.

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