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March 28, 2026Kidney International Reports0 citationsOpen Access

Wcn26-6471 Bevacizumab-Associated Kidney Toxicity in Oncology Patients: An Onconephrology Perspective From a Multi-Ethnic Cohort in Southeast Asia

JWJia Yee WongJWJia Yee WongHLHan Hwa Lee

Key Points

  • To explore the kidney toxicity associated with bevacizumab in oncology patients, particularly focusing on electrolyte disturbances.
  • Case analysis of a multi-ethnic cohort
  • CT scans and urine studies to assess electrolyte levels
  • Hormonal assays to evaluate corticosteroid and ACTH levels
  • Dexamethasone suppression test to confirm Cushing syndrome
  • Severe hypokalemia (2.3 mmol/L) and alkalosis observed after chemotherapy/immunotherapy treatment
  • Recurrence of hyponatremia identified alongside hypercortisolism
  • Electrolyte shifts suggest dual paraneoplastic syndrome potentially linked to small cell lung cancer
  • Normalization of sodium levels achieved through fluid restriction and salt tablets

Abstract

levels.CT scan revealed multiple lung and liver nodules, suggestive of disease recurrence.Instead, liver biopsy confirmed small cell lung cancer, for which chemotherapy/immunotherapy was initiated.Results: Nine months later, she presented with severe hypokalemia (2.3 mmol/L) and alkalosis (CO2 38 mmol/L) but was normonatremic (141) despite not taking her salt tablets.Urine studies revealed renal potassium wasting, and serum studies showed elevated AM cortisol (49.1 mcg/dL) and high ACTH (181 pg/mL).CT scan showed bilateral adrenal thickening.A high-dose dexamethasone suppression test confirmed ectopic Cushing syndrome, so she was started on metyrapone.Within 48 hours, her sodium declined from 138 to 130 mmol/L.Copeptin later came back at >5,000 pmol/L.Tolvaptan was considered, but fluid restriction, salt tablets, and urea normalized her sodium.Conclusion: Hyponatremia resolving to hypokalemia/alkalosis and recurring to hyponatremia again should raise the suspicion for dual paraneoplastic syndrome in SCLC.Our patient exhibited a triphasic electrolyte evolution, highlighting an intricate hormonal interplay: hyponatremia due to SIADH, normalization during hypercortisolism, and recurrent hyponatremia after cortisol reduction.The high cortisol's mineralocorticoid activity, overwhelming 11beta-hydroxysteroid dehydrogenase, likely masked hyponatremia, and then metyraponeinduced cortisol suppression may have unmasked a persistent ADHdriven water retention.Anticipating this triphasic course is key to the diagnosis and treatment of a rare dual paraneoplastic syndrome in SCLC.I have no potential conflict of interest to disclose.I did not use generative AI and AI-assisted technologies in the writing process.

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Cite This Study

Wong et al. (2026) studied this question.

synapsesocial.com/papers/69c770418bbfbc51511e0837https://doi.org/10.1016/j.ekir.2026.105968
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