Zhang Shiyu, Xiong Xingyu, Xie Nan, Zheng Weitao, Li Yongjun, Lin Tianhai, Wei Qiang, Tan Ping
Department of Urology West China Hospital, Sichuan University Chengdu China.
Emergency Department of West China Hospital, West China School of Nursing, Sichuan university Chengdu China.
MedComm (2020). 2024 Apr 24;5(5):e544. doi: 10.1002/mco2.544. eCollection 2024 May.
There is considerable interest in the potential of stereotactic body radiation therapy (SBRT) combined with systemic therapy such as tyrosine kinase inhibitors (TKIs) or immune checkpoint inhibitors (ICIs). However, its efficacy and safety remain unclear. The purpose of this study was to evaluate the efficacy and safety of conducting SBRT during ICI or TKI treatment in different disease settings for patients with metastatic renal cell carcinoma (mRCC). A total of 16 studies were ultimately included. Under the random effects model, the pooled 1-year local control rate (1-yr LCR) and objective response rate (ORR) were 90% (95% confidence interval [CI]: 80%-95%, = 67%) and 52% (95% CI: 37%-67%, = 90%), respectively. SBRT concomitant with different systemic therapy yield significant different 1-yr LCR ( < 0.01) and ORR ( = 0.02). Regarding survival benefits, the pooled 1-year progression-free survival (1-yr PFS) and 1-year overall survival (1-yr OS) rates were 45% (95% CI: 29%-62%, = 91%) and 85% (95% CI: 76%-91%, = 66%), respectively. 1-yr PFS and 1-yr OS in different disease settings demonstrated significant difference ( < 0.01). As for toxicity, the pooled incidence of grade 3-4 adverse events was 14% (95% CI: 5%-26%, = 90%). This study highlights the feasibility of utilizing these strategies in mRCC patients, especially those with a low metastatic tumor burden.
立体定向体部放射治疗(SBRT)联合酪氨酸激酶抑制剂(TKIs)或免疫检查点抑制剂(ICIs)等全身治疗的潜力备受关注。然而,其疗效和安全性仍不明确。本研究的目的是评估在不同疾病背景下,对转移性肾细胞癌(mRCC)患者在ICI或TKI治疗期间进行SBRT的疗效和安全性。最终共纳入16项研究。在随机效应模型下,汇总的1年局部控制率(1-yr LCR)和客观缓解率(ORR)分别为90%(95%置信区间[CI]:80%-95%,I² = 67%)和52%(95% CI:37%-67%,I² = 90%)。与不同全身治疗联合的SBRT产生了显著不同的1年LCR(P < 0.01)和ORR(P = 0.02)。关于生存获益,汇总的1年无进展生存率(1-yr PFS)和1年总生存率(1-yr OS)分别为45%(95% CI:29%-62%,I² = 91%)和85%(95% CI:76%-91%,I² = 66%)。不同疾病背景下的1年PFS和1年OS显示出显著差异(P < 0.01)。至于毒性,3-4级不良事件的汇总发生率为14%(95% CI:5%-26%,I² = 90%)。本研究强调了在mRCC患者中应用这些策略的可行性,尤其是那些转移瘤负荷较低的患者。