Nemes-Tömöri Dóra, Jász Dávid Kurszán, Tari Dóra, Bói Bernadett, Ágoston-Szabó Ágnes, Szűcs Gabriella, Majai Gyöngyike Emese
Division of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Móricz Zsigmond Road 22, 4032 Debrecen, Hungary.
Department of Rheumatology and Immunology, Medical School, University of Pécs, Akác Street 1, 7632 Pécs, Hungary.
Biomedicines. 2025 Apr 19;13(4):993. doi: 10.3390/biomedicines13040993.
: Systemic sclerosis (SSc) is associated with high malignancy risk. With improving SSc management, tumor risk could change, therefore re-evaluating the possibility of neoplasms is necessary. Our aim was to observe malignancy prevalence and its risk factors in the Hungarian SSc population, comparing them to our previous and international results. : We retrospectively collected the data of SSc patients followed by and admitted to three Hungarian clinical centers between 2018 and 2024. The collected data included the characteristics of SSc and neoplasms, autoantibody positivities, immunosuppressive treatments, pregnancy and environmental factors. : Out of 541 patients, 85 had malignancy and, in total, 96 tumors were registered. Skin cancer was the most common ( = 24), followed by breast ( = 14) and lung cancer ( = 14). Among skin cancers, almost one-third was melanoma. Tumors mostly appeared in two peaks: around the time of SSc diagnosis and 10 years later. The occurrence of anti-RNA Polymerase III (anti-RNAPIII) was significantly higher in cancerous patients. Tumor risk was higher with anti-RNAPIII (Odds Ratio (OR) 4.33, 95% Confidence Interval (95% CI) 1.08, 15.1) and anti-topoisomerase I (ATA) (OR 2.34, 95% CI 0.94, 5.84) positivity. Women and patients with diffuse cutaneous SSc (dcSSc) were more likely to have malignancy. Smoking (OR 1.27, 95% CI 0.53, 3.00) also raised the possibility of carcinogenesis. Cancerous patients were older (-value = 0.003), and their mortality was worse compared to non-cancerous patients (Hazard Ratio (HR) 4.75, 95% CI 2.12, 10.62). Pregnancy did not provide a protective effect against breast cancer. : Malignancy significantly contributes to the increased mortality in SSc. Female gender, dcSSc, anti-RNAPIII positivity, smoking and older age represent a higher risk of tumors. Dermatological cancer screening is necessary for all patients with SSc.
系统性硬化症(SSc)与高恶性肿瘤风险相关。随着SSc管理水平的提高,肿瘤风险可能会发生变化,因此有必要重新评估肿瘤发生的可能性。我们的目的是观察匈牙利SSc患者群体中的恶性肿瘤患病率及其风险因素,并将其与我们之前的研究结果和国际研究结果进行比较。
我们回顾性收集了2018年至2024年间在匈牙利三个临床中心接受随访和住院治疗的SSc患者的数据。收集的数据包括SSc和肿瘤的特征、自身抗体阳性情况、免疫抑制治疗、妊娠和环境因素。
在541例患者中,85例患有恶性肿瘤,共登记了96个肿瘤。皮肤癌最为常见(24例),其次是乳腺癌(14例)和肺癌(14例)。在皮肤癌中,近三分之一为黑色素瘤。肿瘤大多出现在两个高峰:SSc诊断时及10年后。癌症患者中抗RNA聚合酶III(anti-RNAPIII)的出现率显著更高。抗RNAPIII(比值比(OR)4.33,95%置信区间(95%CI)1.08,15.1)和抗拓扑异构酶I(ATA)(OR 2.34,95%CI 0.94,5.84)阳性时肿瘤风险更高。女性和弥漫性皮肤型SSc(dcSSc)患者更易发生恶性肿瘤。吸烟(OR 1.27,95%CI 0.53,3.00)也增加了致癌的可能性。癌症患者年龄更大(P值=0.003),与非癌症患者相比,其死亡率更高(风险比(HR)4.75,95%CI 2.12,10.62)。妊娠对乳腺癌没有保护作用。
恶性肿瘤显著导致SSc患者死亡率增加。女性、dcSSc、抗RNAPIII阳性、吸烟和年龄较大代表着更高的肿瘤风险。所有SSc患者都有必要进行皮肤癌筛查。