Jiaju Xu, Lidong Qin, Ping Wang, Zhen Liu, Lili Yang, Hongwei Zhang, Yi Wang, Jiao Gao, Meishu Zhao, Kaili Zhang
Immune checkpoint inhibitors (ICIs) can cause immune-related adverse events (irAEs) affecting multiple organs. Distal renal tubular acidosis (dRTA) as a renal irAE is exceedingly rare, often delaying diagnosis due to nonspecific symptoms. A 63-year-old man with stage IIIA lung squamous cell carcinoma developed recurrent nausea and vomiting after three cycles of nab-paclitaxel/carboplatin combined with tislelizumab. Laboratory evaluation revealed profound metabolic acidosis (CO 2 -CP nadir 11.6 mmol/L) and life-threatening hypokalemia (serum potassium nadir 1.1 mmol/L), requiring ICU admission and mechanical ventilation. Despite aggressive intravenous potassium supplementation (up to 20 mEq/h), hypokalemia paradoxically worsened. Urine pH was 7.0 during systemic acidosis, indicating impaired renal acidification. After excluding other causes, a diagnosis of tislelizumab-induced dRTA was established. Tislelizumab was discontinued, and treatment with oral potassium citrate and prednisone (60 mg/day, tapered over 5.5 months) led to complete resolution of metabolic abnormalities. Over one year of follow-up, the patient has maintained normal renal function without recurrence and achieved a major partial response of his lung cancer. This first reported case of tislelizumab-induced dRTA highlights the need for vigilance when encountering unexplained, potassium-refractory electrolyte disturbances during ICI therapy, emphasizing early diagnosis, drug discontinuation, and pathophysiology-guided therapy.