Madabhavi Irappa, Sarkar Malay, Kumar Vineet, Sagar Raghavendra
Department of Medical and Pediatric Oncology and Hematology, J N Medical College and KLE Academy of Higher Education and Research, Belagavi, India.
Kerudi Cancer Hospital, Bagalkot, India.
Indian J Surg Oncol. 2024 Jun;15(2):321-331. doi: 10.1007/s13193-024-01900-6. Epub 2024 Feb 20.
Head and neck squamous cell carcinomas (HNSCC) have proven to be inherently resistant to systemic treatments as a result of histological, molecular, and etiological heterogeneity, with limited responses seen after second-line therapy and beyond. With limited treatment options after progression on systemic chemotherapy in HNSCCs, immunotherapy has a role to play with improved results. In this prospective, observational, non-randomized, open-label study, a total of 12 patients with advanced, relapsed, or metastatic HNSCC received Inj. Nivolumab weight-based dose of 3 mg per kg, intravenously every 2 weeks along with low-dose capecitabine 500 mg twice a day, was prospectively assessed. The patient's clinical, hematological, and staging characteristics were described and the clinical benefit rate (CBR) was calculated. A total of 12 patients received the combined metronomic chemo-immunotherapy (CMCI). The majority of patients were belonging to ECOG-PS 1(66%), with all patients being in stage IV disease. Six, four, and two patients received immunotherapy as the 5th, 3rd, and 4th line of therapy, respectively. Nivolumab and low-dose capecitabine were used in all 12 patients. CBR was seen in 66% (8/12) of patients, one patient died due to hepatitis and hepatic encephalopathy, another patient died due to pneumonia and respiratory complications, two patients had progressive disease, and two patients with stable disease discontinued treatment because of financial constraints and kept on capecitabine alone. The majority tolerated therapy well with no grade 3/4 immune-related adverse events (IRAEs). Two patients required supportive therapy with packed red cell transfusion and albumin infusions. Six-month overall survival (OS) and progression-free survival (PFS) in the study population were 83.3% and 66.6%, respectively. In conclusion, nivolumab along with metronomic chemotherapy with low-dose capecitabine was very well tolerated and exhibited anti-tumor activity with a CBR of 66%, 6-month OS of 83.3%, and 6-month PFS of 66.6%, in extensively pretreated patients with HNSCCs. Additional studies of nivolumab and metronomic chemotherapy and immuno-immuno combination therapy in these diseases are ongoing.
头颈部鳞状细胞癌(HNSCC)由于组织学、分子学和病因学的异质性,已被证明对全身治疗具有内在抗性,二线及后续治疗的反应有限。在HNSCC患者接受全身化疗进展后治疗选择有限的情况下,免疫疗法发挥了作用并取得了更好的效果。在这项前瞻性、观察性、非随机、开放标签研究中,共有12例晚期、复发或转移性HNSCC患者接受了基于体重的3mg/kg剂量的纳武单抗静脉注射,每2周一次,同时每日两次口服低剂量卡培他滨500mg,并进行了前瞻性评估。描述了患者的临床、血液学和分期特征,并计算了临床获益率(CBR)。共有12例患者接受了节拍化疗免疫联合治疗(CMCI)。大多数患者属于ECOG-PS 1(66%),所有患者均处于IV期疾病。分别有6例、4例和2例患者接受免疫治疗作为第5线、第3线和第4线治疗。所有12例患者均使用了纳武单抗和低剂量卡培他滨。66%(8/12)的患者出现了CBR,1例患者因肝炎和肝性脑病死亡,另1例患者因肺炎和呼吸并发症死亡,2例患者疾病进展,2例病情稳定的患者因经济原因停止治疗,仅继续使用卡培他滨。大多数患者对治疗耐受性良好,无3/4级免疫相关不良事件(IRAEs)。2例患者需要进行浓缩红细胞输血和白蛋白输注的支持治疗。研究人群的6个月总生存期(OS)和无进展生存期(PFS)分别为83.3%和66.6%。总之,在广泛预处理的HNSCC患者中,纳武单抗联合低剂量卡培他滨的节拍化疗耐受性良好,表现出抗肿瘤活性,CBR为66%,6个月OS为83.3%,6个月PFS为66.6%。目前正在对这些疾病中纳武单抗与节拍化疗以及免疫-免疫联合治疗进行更多研究。