Department of Urology, Center for Prostate Cancer, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang-si, Gyeonggi-do, 10408, Republic of Korea.
Biometrics Research Branch, Division of Cancer Epidemiology and Prevention, Research Institute and Hospital of National Cancer Center, Goyang, South Korea.
BMC Cancer. 2019 Jul 15;19(1):688. doi: 10.1186/s12885-019-5900-1.
The differences in progression-free survival (PFS) and cancer-specific survival (CSS) of metastatic renal cell carcinoma (mRCC) patients according to treatment, type of metastasis, and Heng criteria risk are unclear. In this study, we compared survival according to various such parameters.
Between 2000 to 2014, 214 mRCC patients, of whom 171 (79.9%) were intermediate-risk and 43 (20.1%) were poor-risk, were retrospectively selected; 126 (58.9%) patients were treated with immunotherapy (IT) and 88 (41.1%) with targeted therapy (TT). Moreover, 144 patients had synchronous mRCCs (67.3%, SM) and 70 had metachronous mRCCs (32.7%, MM). The Kaplan-Meier method and log-rank test were used to compare progression-free survival (PFS) and CSS.
During a median 4.2 (1.0-70.4) months of systemic treatment and 98.3 (4.8-147.6) months of follow-up, the median PFS and CSS were 4.7 (95% confidence interval [CI]: 3.8-5.5) and 13.8 (95% CI, 9.8-18.3) months, respectively. The PFS and CSS were significantly better in the MM (5.9 and 21.3 months) and intermediate-risk groups (5.2 and 18.3 months) than those in the SM (4.4 and 9.6 months) and poor-risk groups (2.7 and 5.8 months), respectively (p < 0.05). Further stratification showed that TT produced significantly better PFS than IT in intermediate-risk patients with SM and a treatment-free interval (TFI) < 1 year, and in those with MM with a TFI ≥1 year (p < 0.05). There were no differences in survival outcomes according to various other subgroup stratifications (p > 0.05).
Dividing patients into specific subcategories helps to better predict therapeutic outcomes.
转移性肾细胞癌(mRCC)患者的无进展生存期(PFS)和癌症特异性生存期(CSS)的差异因治疗、转移类型和 Heng 标准风险而异。在这项研究中,我们比较了各种参数的生存情况。
在 2000 年至 2014 年间,回顾性选择了 214 名 mRCC 患者,其中 171 名(79.9%)为中危患者,43 名(20.1%)为高危患者;126 名(58.9%)患者接受免疫治疗(IT),88 名(41.1%)接受靶向治疗(TT)。此外,144 名患者为同步性 mRCC(SM),70 名患者为异时性 mRCC(MM)。采用 Kaplan-Meier 法和对数秩检验比较无进展生存期(PFS)和 CSS。
在中位 4.2(1.0-70.4)个月的系统治疗和 98.3(4.8-147.6)个月的随访期间,中位 PFS 和 CSS 分别为 4.7(95%置信区间[CI]:3.8-5.5)和 13.8(95% CI,9.8-18.3)个月。与 SM(4.4 和 9.6 个月)和高危组(2.7 和 5.8 个月)相比,MM(5.9 和 21.3 个月)和中危组(5.2 和 18.3 个月)的 PFS 和 CSS 显著更好(p<0.05)。进一步分层显示,在 SM 中中危患者且治疗无进展间隔(TFI)<1 年和 MM 中 TFI≥1 年的患者中,TT 治疗的 PFS 显著优于 IT(p<0.05)。根据其他亚组分层,生存结果没有差异(p>0.05)。
将患者分为特定亚类有助于更好地预测治疗结果。