This activity is intended for pulmonologists, hematology/oncology specialists, emergency medicine physicians and nurses.
The goal of this activity is to educate members of the multidisciplinary and interprofessional cancer care team on recognizing and understanding how to manage immune-mediated adverse events (imAEs) related to the use of immune checkpoint inhibitors in the management of multiple cancers.
Upon completion of this activity, participants will:
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Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 1.25 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.
Awarded 1.25 contact hour(s) of continuing nursing education for RNs and APNs; 1.25 contact hours are in the area of pharmacology.
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activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 75% on the post-test.
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CME / ABIM MOC / CE Released: 3/25/2019
Valid for credit through: 3/25/2020, 11:59 PM EST
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The following cases are modeled on the interactive grand rounds approach. The questions within the activity are designed to test your current knowledge. After each question, you will be able to see whether you answered correctly and read evidence-based information that supports the most appropriate answer choice. The questions are designed to challenge you; you will not be penalized for answering the questions incorrectly. At the end of the activity, there will be a short post-test assessment based on the material presented.
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Ken is a 55-year-old man who presents to the emergency department (ED) one Sunday with a new nonproductive cough, dyspnea, and shortness of breath. He says he is having difficulty with his daily activities. Ken has a history of hypertension and type 2 diabetes mellitus, for which he is taking metformin and lisinopril. He is a former smoker with a 30-pack year history. Seven months earlier, he received a diagnosis of unresectable stage III squamous cell carcinoma (SCC) of the lung, which had mediastinal node involvement but no distant metastases. His programmed death-ligand 1 (PD-L1) tumor proportion score (TPS) was 2%. He was treated with concurrent platinum-based chemotherapy and radiotherapy. Computed tomography (CT) imaging 2 weeks after completing therapy was without evidence for progression. Ken then received consolidation therapy with durvalumab, a PD-L1 antibody. He has received 9 14-day cycles of intravenous (IV) durvalumab 10 mg/kg, during which he had no progression. A physical examination shows oxygen saturation of 98% on room air, blood pressure of 120/70 mm Hg, a respiratory rate of 24 bpm, and a temperature of 99.9°F. Nothing specific is heard during lung auscultation. Results of a complete blood count (CBC) and other laboratory tests are unremarkable. The ED physician suspects Ken may have checkpoint inhibitor–related pneumonitis (CIP).