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舒尼替尼治疗透明细胞肾细胞癌患者器官毒性的发生率、患病率及其对生存的影响:一家参考癌症中心的经验

Incidence and prevalence of organ toxicities in patients suffering from clear cell renal carcinoma treated with sunitinib and its impact on survival: a reference cancer center experience.

作者信息

Sałek-Zań Agata, Püsküllüoğlu Mirosława, Jaworska Justyna, Pietruszka Agnieszka, Lompart Joanna, Ziobro Marek, Banaś Tomasz

机构信息

Department of Clinical Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Kraków, Poland.

Department of Radiation Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Kraków, Poland.

出版信息

Front Oncol. 2025 Aug 20;15:1590163. doi: 10.3389/fonc.2025.1590163. eCollection 2025.

Abstract

INTRODUCTION

Tyrosine kinase inhibitors (TKIs) are the standard treatment options for advanced clear cell renal cell carcinoma (ccRCC), but their toxicities can hinder optimal dosing, affecting clinical outcomes.

MATERIAL AND METHODS

A retrospective analysis of 96 patients treated with first-line line sunitinib at the National Research Institute of Oncology, Branch Kraków, Poland was conducted to assess the incidence and prevalence of organ toxicities in ccRCC and their impact on overall survival (OS).

RESULTS

The study included 96 patients. The median number of treatment cycles was 11 (IQR: 19), and the median duration was 63 weeks (IQR: 95). The most common toxicities were gastrointestinal (76.0%), fatigue (61.5%), and cardiovascular (49.0%), with 81.3% of patients experiencing multi-organ toxicity. Dose delays occurred in 37 patients (38.5%), mainly due to gastrointestinal (38.5%) and cardiovascular toxicity (21.9%). Dose reductions were required in 64 patients (66.7%), primarily for gastrointestinal (39.6%) and cardiovascular (16.7%) complications. Cardiotoxicity (p=0.017) correlated with improved OS. No OS differences were observed in enterotoxicity, hematologic, endocrine, dermatologic, or renal toxicity. Patients requiring dose reduction due to cardiotoxicity (p=0.012), hematologic toxicity (p=0.004) or gastrointestinal toxicity (p=0.004) had better survival than those without modifications. Patients requiring dose reduction due to any cause had better OS than those maintaining the initial dose. The timing or frequency of dose reductions had no significant impact.

CONCLUSIONS

Cardiotoxicity, gastrointestinal and hematologic toxicities requiring dose reduction were associated with improved survival, suggesting these toxicities may reflect treatment efficacy. The findings emphasize the need to balance toxicity and treatment continuity.

摘要

引言

酪氨酸激酶抑制剂(TKIs)是晚期透明细胞肾细胞癌(ccRCC)的标准治疗选择,但其毒性可能会阻碍最佳剂量的使用,从而影响临床疗效。

材料与方法

对波兰克拉科夫肿瘤研究所国家分院接受一线舒尼替尼治疗的96例患者进行回顾性分析,以评估ccRCC患者器官毒性的发生率和患病率及其对总生存期(OS)的影响。

结果

该研究纳入96例患者。治疗周期的中位数为11(四分位间距:19),持续时间的中位数为63周(四分位间距:95)。最常见的毒性反应为胃肠道毒性(76.0%)、疲劳(61.5%)和心血管毒性(49.0%),81.3%的患者出现多器官毒性。37例患者(38.5%)出现剂量延迟,主要原因是胃肠道毒性(38.5%)和心血管毒性(21.9%)。64例患者(66.7%)需要降低剂量,主要是由于胃肠道并发症(39.6%)和心血管并发症(16.7%)。心脏毒性(p = 0.017)与OS改善相关。在肠毒性、血液学毒性、内分泌毒性、皮肤毒性或肾毒性方面未观察到OS差异。因心脏毒性(p = 0.012)、血液学毒性(p = 0.004)或胃肠道毒性(p = 0.004)而需要降低剂量的患者比未调整剂量的患者生存期更长。因任何原因需要降低剂量的患者比维持初始剂量的患者OS更好。剂量降低的时间或频率没有显著影响。

结论

需要降低剂量的心脏毒性、胃肠道和血液学毒性与生存期改善相关,表明这些毒性可能反映了治疗效果。研究结果强调了平衡毒性和治疗连续性的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f98/12404977/04f60e3f0a24/fonc-15-1590163-g001.jpg

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