Department of Dermatology, University of Turku and Turku University Hospital, Turku, Finland; FICAN West Cancer Research Laboratory, University of Turku and Turku University Hospital, Turku, Finland.
Department of Biostatistics, University of Turku, Turku, Finland.
Acta Derm Venereol. 2024 Nov 27;104:adv40990. doi: 10.2340/actadv.v104.40990.
Actinic keratosis and cutaneous squamous cell carcinoma in situ are precancerous forms of cutaneous squamous cell carcinoma. In this single-centre retrospective study, patients with histopathologically confirmed actinic keratosis (n = 121) or cutaneous squamous cell carcinoma in situ (n = 99) as their initial keratinocyte-derived lesion were compared and evaluated with regard to development of cutaneous squamous cell carcinoma during a 5-year observation period. Patients with severely dysplastic actinic keratosis or cutaneous squamous cell carcinoma in situ as their initial lesion developed cutaneous squamous cell carcinoma more rapidly than patients with actinic keratosis with mild or moderate dysplasia. With either actinic keratosis or cutaneous squamous cell carcinoma in situ as an initial lesion, advanced age, male sex, comorbidity with basal cell carcinoma, and immunosuppressive medication were associated with elevated risk of cutaneous squamous cell carcinoma development. Regarding solely patient with actinic keratosis as their initial lesion male sex, advanced age, immunosuppressive medication, location of the initial lesion, and degree of dysplasia were associated with the risk of cutaneous squamous cell carcinoma. Among patients with cutaneous squamous cell carcinoma in situ as their initial lesion, only aspirin usage was associated with increased risk of cutaneous squamous cell carcinoma. This study indicates that, among the vast and increasing population of patients with cutaneous squamous cell carcinoma precursors, male patients with immunosuppressive medication who develop basal cell carcinoma should be regarded as at heightened risk of cutaneous squamous cell carcinoma development and warrant closer surveillance.
光化性角化病和原位皮肤鳞状细胞癌是皮肤鳞状细胞癌的癌前形式。在这项单中心回顾性研究中,比较了组织病理学证实为光化性角化病(n=121)或原位皮肤鳞状细胞癌(n=99)作为初始角质形成细胞来源病变的患者,并在 5 年观察期内评估了他们发展为皮肤鳞状细胞癌的情况。初始病变为严重发育不良的光化性角化病或原位皮肤鳞状细胞癌的患者比具有轻度或中度发育不良的光化性角化病患者更快地发展为皮肤鳞状细胞癌。无论是光化性角化病还是原位皮肤鳞状细胞癌作为初始病变,年龄较大、男性、基底细胞癌合并症和免疫抑制药物与皮肤鳞状细胞癌发展的风险增加相关。对于仅患有光化性角化病作为初始病变的患者,男性、年龄较大、免疫抑制药物、初始病变的位置和发育不良程度与皮肤鳞状细胞癌的风险相关。在患有原位皮肤鳞状细胞癌作为初始病变的患者中,仅阿司匹林的使用与皮肤鳞状细胞癌的风险增加相关。本研究表明,在患有皮肤鳞状细胞癌前体的庞大且不断增加的患者群体中,患有基底细胞癌且使用免疫抑制药物的男性患者应被视为皮肤鳞状细胞癌发展风险增加的高危人群,并需要更密切的监测。