Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Canada; Department of Oncology, Queen's University, Kingston, Canada.
Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Canada.
Clin Oncol (R Coll Radiol). 2019 Sep;31(9):653-658. doi: 10.1016/j.clon.2019.04.008. Epub 2019 May 2.
Neurotoxicity may affect the quality of life of survivors of testicular cancer. Understanding the burden of neurotoxicity is important to guide survivorship care. A population-based study was undertaken to describe the proportion of patients in the 'real world' with neurotoxicity.
A population-based, retrospective, cohort study of patients with advanced testicular cancer treated in the province of Ontario. The Ontario Cancer Registry was linked to electronic treatment records to identify all incident cases of testicular cancer during 2000-2010. Administrative databases were used to describe health system visits for symptoms potentially related to neurotoxicity. Health system visit rates were explored by number of chemotherapy cycles among patients treated during 2005-2010 for whom complete chemotherapy details were available.
During 2000-2010, 2650 patients underwent an orchiectomy for testicular cancer; 920 (33%) also received chemotherapy. The proportion of patients with health system visits for neurotoxicity in the 2 years before surgery compared with the 2 years after surgery remained stable among patients treated with orchiectomy alone (18% [303/1730] versus 18% [316/1730], P = 0.523); however, there was a substantial increase among patients treated with chemotherapy (16% [151/920] versus 25% [231/920], P < 0.001). Among patients treated with chemotherapy in 2005-2010 for whom complete details were available regarding number of treatment cycles there was a dose-response effect. The increase in health system visits for neurotoxicity from 2 years before compared with 2 years after orchiectomy was greater among patients treated with four cycles of chemotherapy (17% [21/121] versus 37% [45/121]) and three cycles of chemotherapy (17% [45/258] versus 28% [72/258]) compared with those treated with one to two cycles of chemotherapy (<13% [<6/45] versus 20% [9/45], P = 0.013).
This population-based study suggests that symptoms of neurotoxicity are common among survivors of testicular cancer and that this seems to be driven by increasing exposure to chemotherapy. Clinicians should carefully evaluate patients for neurotoxicity during the survivorship phase of treatment.
神经毒性可能会影响睾丸癌幸存者的生活质量。了解神经毒性的负担对于指导生存护理很重要。本研究开展了一项基于人群的研究,旨在描述“真实世界”中患有神经毒性的患者比例。
这是一项基于人群的回顾性队列研究,纳入了在安大略省接受治疗的晚期睾丸癌患者。安大略癌症登记处与电子治疗记录相链接,以确定 2000 年至 2010 年期间所有睾丸癌的发病病例。使用行政数据库来描述与神经毒性相关的潜在症状的就诊情况。通过对 2005 年至 2010 年期间接受完整化疗详细信息的患者进行化疗周期数的探索,来研究患者的就诊率。
2000 年至 2010 年期间,2650 例患者接受了睾丸切除术;其中 920 例(33%)患者还接受了化疗。与术后相比,手术前两年因神经毒性接受医疗系统治疗的患者比例在仅接受睾丸切除术的患者中保持稳定(18%[303/1730]与 18%[316/1730],P=0.523);然而,在接受化疗的患者中,该比例显著增加(16%[151/920]与 25%[231/920],P<0.001)。在 2005 年至 2010 年期间接受了完整化疗周期数详细信息的化疗患者中,存在剂量反应效应。与术后相比,在接受 4 个周期化疗的患者中,因神经毒性而进行医疗系统治疗的就诊率从术前 2 年增加到术后 2 年(17%[21/121]与 37%[45/121]),而在接受 3 个周期化疗的患者中,就诊率增加了(17%[45/258]与 28%[72/258]),与接受 1-2 个周期化疗的患者相比(<13%[6/45]与 20%[9/45],P=0.013)。
本基于人群的研究表明,睾丸癌幸存者普遍存在神经毒性症状,这似乎是由接受化疗的人数增加所驱动的。在治疗的生存阶段,临床医生应仔细评估患者的神经毒性。