Gandarillas Sophia, Tang Horace, Dasgeb Bahar
Department of Dermatology, Wayne State University, Detroit, MI, United States.
Department of Hematology, Community Medical Center, Toms River, NJ, United States.
Front Med (Lausanne). 2024 Mar 11;11:1322210. doi: 10.3389/fmed.2024.1322210. eCollection 2024.
Cutaneous squamous cell carcinoma (cSCC) is the second most common malignancy with the aggressive cSCC subtype being especially worrisome due to its higher metastatic and mortality rate. An 80-year-old immunocompetent Caucasian man presented with a locally advanced and recurrent cSCC for which he underwent six Mohs surgeries, radiation therapy, and standard immunotherapy treatments. Throughout treatment, the patient's cancer continued to progress across different regions of the face. Biopsy and analysis were performed and showed that the cSCCs had a high mutational burden and oncogenes known to be present in tumors with aggressive nature. After the algorithmically applied standard of care failed to cure or control the progressing disease, the genetic analysis favored dostarlimab as a suitable option. With only three doses of 500 mg dostarlimab q3 weeks, the patient showed a fast response with macroscopic resolution of clinically discernible disease of, the previously noted, locally advanced cSCC on his right forehead, as well as other primary keratinocyte carcinomas on his left contralateral face, nose, left leg, and neck. This remarkable case can present an option for complex patients with locally advanced and recurrent cSCC who failed the current standard of care. Moreover, it warrants a proper clinical trial to assess efficacy and potential indication of dostarlimab in such patients. Of note is the presence of a KMT2D mutation and its well-identified correlation with mismatch repair deficiency (dMMR) and poor prognosis, which can play an informative role in clinical decision making and precision therapeutic choice at the point of care.
皮肤鳞状细胞癌(cSCC)是第二常见的恶性肿瘤,侵袭性cSCC亚型因其较高的转移率和死亡率尤其令人担忧。一名80岁免疫功能正常的白种男性患者出现局部晚期复发性cSCC,为此他接受了6次莫氏手术、放射治疗和标准免疫治疗。在整个治疗过程中,患者的癌症在面部不同区域持续进展。进行了活检和分析,结果显示cSCC具有高突变负荷以及已知存在于具有侵袭性肿瘤中的致癌基因。在算法应用的标准治疗未能治愈或控制进展性疾病后,基因分析倾向于选择多斯塔利单抗作为合适的治疗方案。仅给予3剂每3周一次、每次500 mg的多斯塔利单抗,患者就表现出快速反应,临床上可辨别的疾病肉眼可见消退,包括先前所述的右侧前额局部晚期cSCC以及左侧对侧面部、鼻子、左腿和颈部的其他原发性角质形成细胞癌。这个显著的病例为局部晚期复发性cSCC且当前标准治疗失败的复杂患者提供了一种选择。此外,有必要进行适当的临床试验来评估多斯塔利单抗在此类患者中的疗效和潜在适应证。值得注意的是存在KMT2D突变及其与错配修复缺陷(dMMR)和不良预后的明确关联,这在临床决策和即时护理时的精准治疗选择中可发挥参考作用。