Hilser Thomas, Casuscelli Jozefina, Aydogdu Can, Zschäbitz Stefanie, Schnabel Marco Julius, Rinderknecht Emily, Mattigk Angelika, Schostak Martin, Volk Anna-Lisa, Ivanyi Philipp, Wiegmann Jonas, Darr Christopher, Flegar Luka, Mandal Subhajit, Schlack Katrin, Seidl Daniel, Handke Analena, Klee Melanie, Nestler Tim, Rehlinghaus Marc, Hijazi Sameh, Heidenreich Axel, Grünwald Viktor, Paffenholz Pia
Department of Medical Oncology, West German Cancer Center, University Hospital Essen and German Cancer Consortium (DKTK), University Duisburg-Essen, Essen, Germany.
Department of Urology, University Hospital, LMU Munich, Munich, Germany.
Eur Urol Open Sci. 2025 Jul 12;78:59-67. doi: 10.1016/j.euros.2025.06.011. eCollection 2025 Aug.
Papillary renal cell carcinoma (pRCC) is a rare disease. The optimal treatment of metastatic pRCC is still unclear. We evaluated real-world treatment outcomes of first-line treatment in this cohort in Germany.
Patients with advanced or metastatic pRCC were eligible. Adverse events (AEs) were reported according to Common Terminology Criteria for Adverse Events version 5.0. The overall response rate was accessed according to the local standard. Progression-free survival (PFS) was calculated from the start of treatment to progression or death. Descriptive statistics and Kaplan-Meier plots were utilised, where appropriate.
In total, 121 suitable patients (77% male) with a median age of 63 yr (quartiles 55, 70) were included. Prior nephrectomy was performed in 78%. Eastern Cooperative Oncology Group performance status 0-1 was reported in 74%. Lymphatic (68%) and pulmonary (42%) metastases were most common. Of the patients, 59% received first-line immune checkpoint inhibitor (ICI) combination therapies (ICI-ICI: 20%, tyrosine kinase inhibitor [TKI]-ICI: 39%), and 41% of patients received TKI monotherapy, predominantly sunitinib. The median follow-up time was 33.3 mo (interquartile range 14.8-46.7). The median PFS was 5.4 mo (95% confidence interval [CI]: 3.2-7.6) for ICI-ICI combinations, 16.9 mo (95% CI: 7.2-26.6) for ICI-TKI combinations, and 8.8 mo (95% CI: 7.0-10.7) for TKI monotherapy. Of all the patients, 70% and 35% experienced all-grade and grade 3-5 AEs, respectively. AEs of any cause led to discontinuation in 33% of patients.
TKI-based therapies are applied frequently in pRCC patients. Our data support the use of ICI plus TKI as a first-line standard for patients with pRCC. The major limitations were the retrospective data capture and short follow-up of our study. Additional analyses to tailor treatment strategies in patients with metastatic pRCC are warranted.
In this report, we looked at the outcome of first-line treatment of patients with metastatic papillary renal cell cancer (pRCC). Tyrosine kinase inhibitor (TKI)-based therapies are applied frequently in pRCC. Our data support the use of immune checkpoint inhibitor plus TKI as a first-line standard for patients with pRCC. However, further studies are needed to optimise treatment in patients with metastatic pRCC.
乳头状肾细胞癌(pRCC)是一种罕见疾病。转移性pRCC的最佳治疗方案仍不明确。我们评估了德国这一队列中一线治疗的真实世界治疗结果。
纳入晚期或转移性pRCC患者。不良事件(AE)根据不良事件通用术语标准第5.0版进行报告。根据当地标准评估总缓解率。无进展生存期(PFS)从治疗开始计算至疾病进展或死亡。在适当情况下使用描述性统计和Kaplan-Meier曲线。
共纳入121例合适患者(77%为男性),中位年龄63岁(四分位数间距为55、70)。78%的患者曾接受过肾切除术。74%的患者东部肿瘤协作组体能状态为0 - 1。最常见的转移部位是淋巴结(68%)和肺部(42%)。59%的患者接受一线免疫检查点抑制剂(ICI)联合治疗(ICI - ICI:20%,酪氨酸激酶抑制剂[TKI] - ICI:39%),41%的患者接受TKI单药治疗,主要是舒尼替尼。中位随访时间为33.3个月(四分位数间距为14.8 - 46.7)。ICI - ICI联合治疗的中位PFS为5.4个月(95%置信区间[CI]:3.2 - 7.6),ICI - TKI联合治疗为16.9个月(95% CI:7.2 - 26.6),TKI单药治疗为8.8个月(95% CI:7.0 - 10.7)。所有患者中,分别有70%和35%经历了所有级别的AE和3 - 5级AE。任何原因导致的AE使33%的患者停药。
基于TKI的治疗方法在pRCC患者中应用频繁。我们的数据支持将ICI加TKI作为pRCC患者的一线标准治疗方案。主要局限性在于本研究为回顾性数据收集且随访时间较短。有必要进行额外分析以制定转移性pRCC患者的治疗策略。
在本报告中,我们观察了转移性乳头状肾细胞癌(pRCC)患者一线治疗的结果。基于酪氨酸激酶抑制剂(TKI)的治疗方法在pRCC中应用频繁。我们的数据支持将免疫检查点抑制剂加TKI作为pRCC患者的一线标准治疗方案。然而,需要进一步研究以优化转移性pRCC患者的治疗。