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Ⅰ期精原细胞瘤的治疗选择。

Treatment options in stage I seminoma.

机构信息

Clinic of Urology, University Clinical Center of Serbia, Belgrade, 11000, Serbia.

Faculty of Medicine, University of Belgrade, Belgrade, 11000, Serbia.

出版信息

Oncol Res. 2023 Jan 12;30(3):117-128. doi: 10.32604/or.2022.027511. eCollection 2022.

DOI:10.32604/or.2022.027511
PMID:37305015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10208057/
Abstract

Seminomas are most commonly diagnosed in clinical stage I (CSI). After orchiectomy, approximately 15% of patients in this stage have subclinical metastases. Adjuvant radiotherapy (ART) delivered to the retroperitoneum and ipsilateral pelvic lymph nodes has been the mainstay of treatment for many years. Although highly efficient, with long-term cancer-specific survival (CSS) rates approaching almost 100%, ART is associated with considerable long-term consequences, particularly cardiovascular toxicity and increased risk of secondary malignancies (SMN). Therefore, active surveillance (AS) and adjuvant chemotherapy (ACT) were developed as alternative treatment options. While AS prevents patient overtreatment, it is associated with strict follow-up regimens and increased radiation exposure due to repeated imaging. Due to equivalent CSS rates to ART, and lower toxicity, one course of adjuvant carboplatin presents the cornerstone of chemotherapy for CSI patients. CSS is almost 100% for patients with CSI seminoma, regardless of the chosen treatment option. Therefore, a personalized approach in treatment selection is preferred. Currently, routine radiotherapy for CSI seminoma patients is no longer recommended. Instead, it should be reserved for patients who are unfit or unwilling for AS or ACT. Identification of prognostic factors for disease relapse allowed for the development of risk-adapted treatment strategy and stratification of patients in low-risk and high-risk groups. Although risk-adapted policy needs further validation, surveillance is currently recommended in low-risk patients, while ACT is reserved for patients with a higher risk of relapse.

摘要

精原细胞瘤最常被诊断为临床 I 期(CSI)。在睾丸切除术之后,大约 15%的 CSI 患者存在亚临床转移。多年来,腹膜后和同侧骨盆淋巴结的辅助放疗(ART)一直是主要的治疗方法。虽然 ART 非常有效,长期癌症特异性生存率(CSS)接近 100%,但它也伴随着相当大的长期后果,特别是心血管毒性和继发性恶性肿瘤(SMN)风险增加。因此,主动监测(AS)和辅助化疗(ACT)被开发为替代治疗选择。虽然 AS 可以防止患者过度治疗,但它与严格的随访方案相关,并且由于重复成像导致辐射暴露增加。由于与 ART 的 CSS 率相当,并且毒性较低,因此辅助卡铂治疗方案成为 CSI 精原细胞瘤患者化疗的基石。CSI 精原细胞瘤患者的 CSS 几乎为 100%,无论选择何种治疗方案。因此,在治疗选择中采用个性化方法是首选。目前,不再推荐对 CSI 精原细胞瘤患者进行常规放疗。相反,它应该保留给不适合或不愿意接受 AS 或 ACT 的患者。识别疾病复发的预后因素允许制定风险适应治疗策略,并对低危和高危患者进行分层。尽管风险适应策略需要进一步验证,但目前建议对低危患者进行监测,而高危患者则保留 ACT。