Efficacy and safety of cabozantinib in metastatic renal cell carcinoma patients: Russian multicenter observational study

M. Volkova, A. Kalpinskiy, K. V. Men'shikov, L. V. Gorbuleva, O. Evsyukova, V. R. Meltonyan, S. Mishugin, M. R. Maturov, A. S. Ol'shanskaya, D. Y. Shemetov, T. Sannikova, M. V. Makhnutina, M. A. Filip'eva, E. Gaysina, E. Ovchinnikova, V. Matveev, B. Alekseev
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Abstract

Purpose: an assessment of efficacy and safety of cabozantinib in unselected patients with metastatic renal cell carcinoma in the first and subsequent lines of therapy.Materials and methods. Russian multicenter observational study included 92 consecutive patients with morphologically verified metastatic renal cell carcinoma treated with cabozantinib (60 mg/d) in 16 Russian centers. Median age of the patients was 56 (19-79) years, a male-to-female ratio - 3:1. At the start of cabozantinib therapy 27.2 % of patients had ECOG PS 2. Most common histological type of kidney cancer was clear-cell RCC (90.2 %). Most patients were diagnosed with synchronous (71.7 %) multiple metastases (60.9 %). Previous nephrectomy was performed in 87.0 % of cases. Prognosis according to International Metastatic Renal Cancer Database Consortium (IMDC) score was assessed as favorable in 5.4 %, intermediate - in 58.7 % and poor - in 35.9 % patients. Cabozantinib as the first-line therapy was administered in 9 (9.8 %), following 1-5 lines of systemic treatment - in 83 (90.2 %) cases. Median follow-up was 11 (2.3-44.5) months.Results. In patients, receiving cabozantinib as the first-line therapy, objective response rate was 66.7 %, tumor control was reached in 100 % of cases. Median time to the objective response was 2.6 (1.9-3.6) months, median objective response duration - 13.2 (6.2-21.5) months. Median progression-free survival (PFS) and overall survival (OS) were not reached, 6- and 12-months PFS was 77.8 % and 77.8 %, 6- and 12-months OS - 88.9 % and 88.9 % respectively. Cabozantinib as the second and subsequent lines of therapy provided objective response rate of 34.9 %, tumor control rate - 97.6     %. Median time to the objective response was 2.5 (1.8-4.1) months, median objective response duration - 12.6 (5.5-27.3) months. Median PFS was not reached (6- and 12-months PFS - 92.5 % and 73.1 % respectively), median OS was 32.6      months (6- and 12-months OS - 97.4 % and 80.8 % respectively). Any adverse events (AE) developed in 88.8 %, AE grade III-IV - in 32.6 % of cases. Most frequent AE grade III-IV included arterial hypertension (18.5 %), diarrhea (6.5 %) and palmar-plantar erythrodysesthesia (6.5 %). Unacceptable toxicity demanded treatment cancellation in 2.2 %, therapy interruption - in 16.3 % and dose reduction - in 30.4 % of patients.Conclusion. Cabozantinib as the first and subsequent lines of therapy for metastatic renal cell carcinoma patients in the real world practice demonstrated high efficacy and better tolerability comparing with population assigned for cabozantinib monotherapy in the randomized phase II-III trials.
卡博赞替尼在转移性肾细胞癌患者中的疗效和安全性:俄罗斯多中心观察性研究
目的:评估卡博赞替尼在未选择的转移性肾细胞癌患者的一线和后续治疗中的有效性和安全性。材料和方法。俄罗斯多中心观察性研究包括在16个俄罗斯中心连续92例经形态学证实的转移性肾细胞癌患者接受卡博赞替尼(60 mg/d)治疗。患者中位年龄56(19-79)岁,男女比例- 3:1。在卡博赞替尼治疗开始时,27.2%的患者ECOG ps2。肾癌最常见的组织学类型是透明细胞肾细胞癌(90.2%)。大多数患者被诊断为同步(71.7%)多发性转移(60.9%)。87%的病例曾行过肾切除术。根据国际转移性肾癌数据库联盟(IMDC)评分,5.4%的患者预后良好,58.7%为中等,35.9%为不良。9例(9.8%)患者接受卡博赞替尼作为一线治疗,83例(90.2%)患者接受1-5线全身治疗。中位随访时间为11(2.3-44.5)个月。在接受卡博赞替尼作为一线治疗的患者中,客观有效率为66.7%,100%的病例达到肿瘤控制。中位客观反应时间为2.6(1.9-3.6)个月,中位客观反应持续时间为13.2(6.2-21.5)个月。中位无进展生存期(PFS)和总生存期(OS)未达到,6个月和12个月的PFS分别为77.8%和77.8%,6个月和12个月的OS分别为88.9%和88.9%。卡博赞替尼作为二线及后续治疗的客观缓解率为34.9%,肿瘤控制率为97.6%。客观缓解的中位时间为2.5(1.8-4.1)个月,客观缓解的中位持续时间为12.6(5.5-27.3)个月。未达到中位PFS(6个月和12个月PFS分别为92.5%和73.1%),中位OS为32.6个月(6个月和12个月OS分别为97.4%和80.8%)。不良事件(AE)发生率为88.8%,AE III-IV级发生率为32.6%。最常见的AE III-IV级包括动脉高血压(18.5%)、腹泻(6.5%)和掌足底红觉不良(6.5%)。不可接受的毒性要求2.2%的患者取消治疗,16.3%的患者中断治疗,30.4%的患者减少剂量。Cabozantinib作为转移性肾细胞癌患者的一线和后续治疗,在现实世界的实践中,与随机II-III期试验中分配给Cabozantinib单药治疗的人群相比,显示出更高的疗效和更好的耐受性。
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