The Meaning of Lymphadenopathies During Adjuvant Durvalumab After Chemoradiotherapy for Lung Cancer: Thinking Beyond Disease Progression

• Published in: Curēus (Palo Alto, CA) Vol. 14; no. 7; p. e26729
• Main Authors: Pantarotto, Marcos, Barata, Rita, Coelho, Ricardo, Carvalheiro, Catarina, Rolim, Ines, Garrido, Patricia, GIl, Nuno, Duarte-Ramos, Filipa, Tonin, Fernanda S
• Format: Journal Article
• Language: English
• Published: United States Cureus Inc 11.07.2022; Cureus
• Subjects: Antigens; Asymptomatic; Biopsy; Cancer therapies; Case reports; Chemotherapy; Cytotoxicity; Diagnostic tests; Epidermal growth factor; Granulomas; Immunotherapy; Inflammation; Ligands; Lung cancer; Lymphatic system; Medical diagnosis; Medical imaging; Melanoma; Monoclonal antibodies; Oncology; Patients; Pulmonology; Radiation therapy; Sarcoidosis; Skin; Targeted cancer therapy; Therapeutics; Tomography; Ultrasonic imaging; lung cancer; pseudoprogression; differential diagnosis; immune-checkpoint inhibitors; immune-related adverse events
• ISSN: 2168-8184; 2168-8184
• DOI: 10.7759/cureus.26729

Immune-checkpoint inhibitors (ICIs) have become the mainstay of treatment for many malignancies. With this new strategy, relevant immune-related adverse events (irAEs) have been reported, some of which can be mistaken for disease progression. To better illustrate the current challenges in diagnosing and managing a patient under adjuvant ICI treatment, we present the case of a 67-year-old female patient with stage IIIB unresectable, epidermal growth factor receptor (EGFR)-mutated, non-small-cell lung cancer who was initially treated with chemoradiotherapy, followed by immunotherapy with durvalumab. During the course of immunotherapy, the patient presented with madarosis and erythematous and endured skin lesions, in addition to lymphadenopathies and pulmonary infiltrates. She was started on first-line palliative treatment with an EGFR tyrosine kinase inhibitor. After reviewing the case, a multidisciplinary team meeting suggested diagnostic procedures, including a transbronchial needle aspiration from mediastinal lymph nodes. The histologic examination showed chronic systemic inflammation and non-caseating granulomas of the sarcoid type. In this case, palliative treatment was suspended and systemic therapy with prednisolone was initiated. The patient became asymptomatic and the previously observed radiologic abnormalities resolved. This case highlights the importance of early recognition and appropriate treatment of irAEs, mainly because these conditions remain poorly understood and are probably underdiagnosed. Considering differential diagnosis is paramount to guide clinical management, despite curative or palliative treatment intent.