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1.
Immunotherapy ; 15(6): 417-428, 2023 04.
Article in English | MEDLINE | ID: mdl-37013834

ABSTRACT

Introduction: Immune checkpoint inhibitor-associated diabetes mellitus (ICI-DM) is a rare adverse event. In this study, we characterize clinical outcomes of patients with ICI-DM and evaluate survival impact of this complication on melanoma patients. Research design & methods: We conducted a retrospective review of 76 patients diagnosed with ICI-DM from April 2014 to December 2020. Results: 68% of patients presented in diabetic ketoacidosis, 16% had readmissions for hyperglycemia, and hypoglycemia occurred in 70% of patients after diagnosis. Development of ICI-DM did not impact overall survival or progression-free survival in melanoma patients. Conclusion: Development of ICI-DM is associated with long-term insulin dependence and pancreatic atrophy; the use of diabetes technology in this patient population can help improve glycemic control.


Cancer treatment with immune checkpoint inhibitors can cause irreversible side effects. In this study, we describe the clinical presentations of 76 patients who developed immune checkpoint inhibitor diabetes mellitus, a rare complication of checkpoint inhibitor therapy that requires lifelong treatment with insulin therapy. Most patients presented with a life-threatening hyperglycemic emergency and had experienced weight loss and hyperglycemia several weeks prior to diagnosis. After diagnosis, these patients are at risk for high and low blood sugars, but the use of glucose monitoring devices and insulin pumps can help improve blood sugar control. In our study, the development of this complication did not affect survival for melanoma patients. We need to improve awareness of this rare complication to ensure timely treatment for patients.


Subject(s)
Diabetes Mellitus , Melanoma , Humans , Immune Checkpoint Inhibitors/therapeutic use , Melanoma/drug therapy , Retrospective Studies
2.
J Clin Ultrasound ; 48(4): 227-230, 2020 May.
Article in English | MEDLINE | ID: mdl-32045024

ABSTRACT

Metastases to the submandibular gland are extremely rare; a literature search retuned only three previously reported cases from a thyroid gland primary site. Herein, we report two cases of metastatic thyroid carcinoma to the submandibular gland in a 64-year-old woman with PTC and a 70-year-old-woman with medullary thyroid carcinoma (MTC). The metastases were identified on CT and PET/CT in one case and on CT in the other case, but both were diagnosed with ultrasound-guided fine-needle aspiration. Our cases highlight that while rare, both PTC and MTC can metastasize to the submandibular gland.


Subject(s)
Carcinoma, Neuroendocrine/secondary , Submandibular Gland Neoplasms/secondary , Thyroid Cancer, Papillary/secondary , Thyroid Neoplasms/pathology , Aged , Biopsy, Fine-Needle , Calcitonin/metabolism , Carcinoma, Neuroendocrine/diagnostic imaging , Carcinoma, Neuroendocrine/metabolism , Female , Humans , Middle Aged , Positron Emission Tomography Computed Tomography , Submandibular Gland Neoplasms/diagnostic imaging , Thyroid Cancer, Papillary/diagnostic imaging , Thyroid Cancer, Papillary/metabolism , Thyroid Neoplasms/diagnostic imaging , Thyroid Neoplasms/metabolism , Thyroid Neoplasms/secondary , Thyroidectomy , Tomography, X-Ray Computed , Ultrasonography
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