Ashraf Sara, Alsharedi Mohamed
Joan C Edwards School of Medicine at Marshall University, Huntington, West Virginia, USA.
Stem Cell Investig. 2021 Sep 6;8:19. doi: 10.21037/sci-2020-071. eCollection 2021.
The most common cancer in the United States is non-melanoma skin cancer. Cutaneous squamous cell carcinoma (cSCC) is the second most common non-melanoma skin cancer after basal cell carcinoma. It develops in the middle and outer layers of the skin. Its precursor is actinic keratosis, which can progress to squamous cell carcinoma in situ, invasive cSCC, and finally metastatic cSCC. About 20% of non-melanoma skin cancers are squamous cell and the remaining 80% are basal cell. Unlike basal cell, squamous cell carcinoma has the propensity to metastasize. This commonly occurs with squamous cell carcinoma (SCC) thicker than 2 millimeters. The risk of metastasis and local recurrence increases with 6 mm thickness and desmoplasia. The risk factors are excessive sun or ultraviolet light (tanning beds) exposure, immunosuppression (either having a weakened immune system or taking immunosuppressive therapy) and fair skin. Therefore, it most commonly affects skin in the head and neck area such as scalp, ears, lips, face, neck or the back of the hands. The treatment for local cutaneous squamous cell cancer is mainly surgery; excisional surgery, Moh's surgery, cryosurgery, curettage and electrodessication, laser surgery or radiation therapy, photodynamic therapy or topical agents such as fluorouracil or imiquimod. However, cSCC that is locally advanced, such as involvement of regional lymph nodes, or has metastasized to distant organs or tissue, is not amenable to surgery or radiation alone. Immunotherapy with cemiplimab, a programmed cell death 1 (PD-1) inhibitor, is a US Food and Drug Administration (FDA) approved therapeutic option for locally advanced and metastatic cSCC for patients who are not candidates for or whose disease is not susceptible to curative surgery or radiation therapy. Cemiplimab is a humanized recombinant immunoglobulin monoclonal antibody that binds to and blocks PD-1 receptor found on T cells inhibiting T-cell proliferation and cytokine production. We present a case of locally advanced cSCC with regional lymph nodes metastases, which achieved clinical remission, utilizing a unique approach of therapy combining a checkpoint inhibitor, Cemiplimab and radiotherapy.
美国最常见的癌症是非黑色素瘤皮肤癌。皮肤鳞状细胞癌(cSCC)是仅次于基底细胞癌的第二常见非黑色素瘤皮肤癌。它发生在皮肤的中层和外层。其前体是光化性角化病,可进展为原位鳞状细胞癌、侵袭性cSCC,最终发展为转移性cSCC。约20%的非黑色素瘤皮肤癌为鳞状细胞癌,其余80%为基底细胞癌。与基底细胞癌不同,鳞状细胞癌有转移倾向。这种情况通常发生在厚度超过2毫米的鳞状细胞癌(SCC)中。转移和局部复发的风险随着厚度达到6毫米和出现促结缔组织增生而增加。风险因素包括过度日晒或紫外线(晒黑床)暴露、免疫抑制(免疫系统较弱或接受免疫抑制治疗)以及皮肤白皙。因此,它最常影响头颈部区域的皮肤,如头皮、耳朵、嘴唇、面部、颈部或手背。局部皮肤鳞状细胞癌的治疗主要是手术,包括切除手术、莫氏手术、冷冻手术、刮除术和电干燥法、激光手术或放射治疗、光动力疗法或外用药物,如氟尿嘧啶或咪喹莫特。然而,局部晚期的cSCC,如区域淋巴结受累,或已转移至远处器官或组织,则不适合单独进行手术或放疗。使用西米普利单抗(一种程序性细胞死亡1(PD-1)抑制剂)进行免疫治疗,是美国食品药品监督管理局(FDA)批准的一种治疗选择,用于治疗局部晚期和转移性cSCC,适用于不适合或对根治性手术或放射治疗不敏感的患者。西米普利单抗是一种人源化重组免疫球蛋白单克隆抗体,它与T细胞上发现的PD-1受体结合并阻断该受体,抑制T细胞增殖和细胞因子产生。我们报告了一例局部晚期cSCC伴区域淋巴结转移的病例,该病例采用了一种独特的治疗方法,将检查点抑制剂西米普利单抗与放疗相结合,实现了临床缓解。