Division Genitourinary Oncology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Hospital Universitario La Fe de Valencia, Valencia, Spain.
Clin Transl Oncol. 2020 Sep;22(9):1517-1523. doi: 10.1007/s12094-020-02288-9. Epub 2020 Feb 11.
BACKGROUND (OR PURPOSE): Nivolumab has been shown to be effective for the treatment of second-line mRCC. The present study has investigated the effectiveness and safety of nivolumab in real-world Eastern Spanish patients with advanced mRCC at TKI progression.
A retrospective review of mRCC patients treated with nivolumab as a second-line treatment was performed. Analyzed variables included age, sex, ECOG (quality of life scale designed by the Eastern Cooperative Oncology Group), histology, nephrectomy, location of metastases, number of metastasis locations, previous treatments, analytical data from the standard blood count and biochemistry, and response to treatment.
98 patients from 18 sites in Spain were retrospectively reviewed. The majority of patients were male (75%), had ECOG 0-1 (90.6%), had no brain metastasis (91.4%), had undergone one prior systemic regimen (94.3%), and were current/former smokers (97.1%). Fourteen patients (13.1%) had non-clear cell histology, seven (7.1%) had poor-IMDC prognostic group characteristics, 13 patients (13.1%) had liver metastasis and 35 (35.7%) had bone lesions. All patients received prior systemic therapy (63.3% sunitinib, 34.7% pazopanib). During the study, a median of eight doses of nivolumab was given (range 2-62) and 11 patients received more than 12 doses. Eleven patients (11.2%) received nivolumab as a third or fourth line of treatment. Median duration of therapy was 3.6 months (range 0.5-29.3). Confirmed response rate was 25%. Median progression free survival was 7.8 months (range 1.2-12.1). Median overall survival was 16.3 months (range 1.7-29.3). After discontinuation of treatment, 27.58% of the patients received subsequent systemic cancer therapy. Side effects were mostly grade 1-2 (7.2% had hypothyroidism and 6.2% liver toxicity, 4% had nephritis and 2% hypophysitis). Two cases of grade 3-4 adverse events (2%) were reported.
Benefit/risk profile of nivolumab in Eastern-Spanish real-world population with mRCC after tyrosine-kinase inhibitors was consistent with prior real-life studies reported as well as pivotal study.
背景(或目的):纳武利尤单抗已被证明可有效治疗二线转移性肾细胞癌(mRCC)。本研究调查了纳武利尤单抗在西班牙东部接受过酪氨酸激酶抑制剂(TKI)进展后的晚期 mRCC 二线治疗的真实世界中对患者的疗效和安全性。
对接受纳武利尤单抗二线治疗的 mRCC 患者进行了回顾性分析。分析的变量包括年龄、性别、ECOG(东部合作肿瘤组设计的生活质量量表)、组织学、肾切除术、转移部位、转移部位数量、既往治疗、标准血常规和生化分析数据以及治疗反应。
西班牙 18 个地点的 98 例患者进行了回顾性分析。大多数患者为男性(75%),ECOG 0-1(90.6%),无脑转移(91.4%),接受过一次系统治疗(94.3%),且为当前/既往吸烟者(97.1%)。14 例(13.1%)患者组织学为非透明细胞,7 例(7.1%)患者不良 IMDC 预后组特征,13 例(13.1%)患者有肝转移,35 例(35.7%)有骨病变。所有患者均接受过系统治疗(63.3%舒尼替尼,34.7%帕唑帕尼)。研究期间,中位纳武利尤单抗剂量为 8 个(范围 2-62),11 例患者接受了超过 12 个剂量。11 例(11.2%)患者接受纳武利尤单抗作为三线或四线治疗。中位治疗持续时间为 3.6 个月(范围 0.5-29.3)。确认的缓解率为 25%。中位无进展生存期为 7.8 个月(范围 1.2-12.1)。中位总生存期为 16.3 个月(范围 1.7-29.3)。治疗停止后,27.58%的患者接受了后续的系统癌症治疗。副作用大多为 1-2 级(7.2%甲状腺功能减退,6.2%肝毒性,4%肾炎,2%垂体炎)。报告了 2 例 3-4 级不良事件(2%)。
纳武利尤单抗在西班牙东部真实世界 mRCC 人群中的获益/风险特征与先前报告的真实世界研究以及关键研究一致。