Why the study?
Alveolar soft part sarcoma is a rare malignancy with low sensitivity to chemotherapy and substantially decreased 5-year overall survival in metastatic disease.
Does pembrolizumab combined with axitinib improve tumor response in an elderly patient with metastatic alveolar soft part sarcoma and autoimmune disorders?
Does pembrolizumab combined with axitinib improve tumor response in an elderly patient with metastatic alveolar soft part sarcoma and autoimmune disorders?
Pembrolizumab combined with axitinib can be an effective and safe treatment for metastatic alveolar soft part sarcoma even in elderly patients with pre-existing autoimmune disorders.
Suggests pembrolizumab plus axitinib may be feasible in elderly sarcoma patients with autoimmune comorbidities;.
Alveolar soft part sarcoma (ASPS) is a rare malignancy with low sensitivity to chemotherapy. While localized ASPS has a very good prognosis after resection, the 5-year overall survival rate drops substantially in metastatic disease. We report the case of an 80-year-old male patient with ASPS of the left elbow and metastasis to the lung, lymph nodes and peritoneum. After weighing the benefits and risks, systemic treatment with the anti-PD-1 checkpoint inhibitor pembrolizumab combined with the vascular endothelial growth factor receptor tyrosinkinase inhibitor axitinib was initiated in this patient with a history of psoriasis and Crohn's disease. After only two cycles of therapy, a significant size reduction of the nodal cervical metastasis became apparent. A partial response of all metastases was then confirmed in the first computed tomography restaging. So far, side effects have remained manageable, especially with regard to the development or worsening of autoimmune adverse events. The patient continued to have a high quality of life, while also remaining in ongoing partial response for 15 months at the time of submission. While sarcomas generally have low sensitivity to immunotherapies, ASPS is an exception, and checkpoint inhibition is an integral part of its systemic therapy.
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Dorman et al. (2022) studied this question.
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