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年龄≥40 岁与转移性生殖细胞癌的不良结局相关,尽管接受了适当的意向化疗。

Age ≥40 Years Is Associated with Adverse Outcome in Metastatic Germ Cell Cancer Despite Appropriate Intended Chemotherapy.

机构信息

University College London Hospital, London, UK; Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

Eur Urol Focus. 2017 Dec;3(6):621-628. doi: 10.1016/j.euf.2016.10.005. Epub 2016 Oct 26.

Abstract

BACKGROUND

Age ≥40 yr is associated with poorer testicular cancer outcomes in population-based studies.

OBJECTIVE

To assess the association between age (≥40 yr) and outcomes among men with germ cell tumors (GCTs) in a large hospital registry.

DESIGN, SETTING, AND PARTICIPANTS: Electronic medical records for 1095 GCT patients treated at Dana-Farber Cancer Institute between 1997 and 2013 were reviewed. Information regarding histology, stage, treatment, and patient characteristics was obtained.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

Using logistic regression analysis and Cox proportional hazards regression, we investigated the association between age and treatment and risk of relapse and GCT-specific death for men with GCT.

RESULTS AND LIMITATIONS

At diagnosis, 26% of men (n=283/1095) were ≥40 yr. Among the 610 men with clinical stage 1 (CS1) disease, age ≥40 yr was not associated with a higher risk of CS1 relapse (hazard ratio [HR] 1.19, 95% confidence interval [CI] 0.74-1.92). There were 603 men with metastatic disease (CS1 at diagnosis with subsequent relapse or metastasis at diagnosis); after adjusting for stage and histology, men ≥40 yr were more likely to receive etoposide and cisplatin chemotherapy compared to bleomycin, etoposide, and cisplatin as their primary treatment (odds ratio 2.40, 95% CI 1.14-5.05). Salvage therapy also differed by age. In the multivariable model, men ≥40 yr with metastatic GCT had a higher risk of relapse (HR 1.58, 95% CI 1.02-2.46) after primary treatment and death from GCT (HR 2.31, 95% CI 1.29-4.15). The study limitations include incomplete data on medical comorbidities and possible subsequent dose modifications.

CONCLUSIONS

Men aged ≥40 yr with metastatic GCT have poorer outcomes, even after accounting for different intended treatment patterns.

PATIENT SUMMARY

In this study we looked at the outcome for testicular cancer in more than 1000 patients treated at a single institution in the USA. We found that the treatment for metastatic disease differed between older (≥40 yr) and younger patients. Furthermore, outcomes for older patients (≥40 yr) were worse than for younger men.

摘要

背景

基于人群的研究表明,年龄≥40 岁与睾丸癌结局较差相关。

目的

评估在大型医院登记处中,年龄(≥40 岁)与生殖细胞瘤(GCT)男性患者结局之间的关联。

设计、设置和参与者:回顾了 1997 年至 2013 年间在 Dana-Farber 癌症研究所接受治疗的 1095 名 GCT 患者的电子病历。获取了有关组织学、分期、治疗和患者特征的信息。

结局测量和统计分析

使用逻辑回归分析和 Cox 比例风险回归,我们调查了年龄与 GCT 男性的治疗和复发风险以及 GCT 特异性死亡之间的关系。

结果和局限性

在诊断时,26%的男性(n=283/1095)年龄≥40 岁。在 610 名患有临床分期 1(CS1)疾病的男性中,年龄≥40 岁与 CS1 复发的风险增加无关(危险比[HR]1.19,95%置信区间[CI]0.74-1.92)。有 603 名患有转移性疾病(CS1 在诊断时随后复发或在诊断时发生转移)的男性;在调整了分期和组织学后,与博来霉素、依托泊苷和顺铂相比,年龄≥40 岁的男性更有可能接受依托泊苷和顺铂化疗作为其主要治疗方法(优势比 2.40,95%CI1.14-5.05)。挽救性治疗也因年龄而异。在多变量模型中,接受转移性 GCT 治疗的年龄≥40 岁的男性在接受主要治疗后复发的风险较高(HR1.58,95%CI1.02-2.46),并且死于 GCT 的风险较高(HR2.31,95%CI1.29-4.15)。研究的局限性包括对合并症和可能随后进行剂量调整的不完全数据。

结论

即使考虑到不同的预期治疗模式,年龄≥40 岁的患有转移性 GCT 的男性结局仍较差。

患者总结

在这项研究中,我们观察了在美国一家医疗机构接受治疗的 1000 多名患者的睾丸癌结局。我们发现,年龄较大(≥40 岁)和较年轻的患者之间转移性疾病的治疗方法不同。此外,年龄较大(≥40 岁)的患者的结局比年轻男性差。

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