Stage IIIB non-squamous NSCLC on chemoimmunotherapy: alcohol-related hypertonic hyponatremia corrected during oncology follow-up

This lung cancer diagnosis at a glance

Stage at diagnosis
Stage III
Subtype
Non-Small Cell Lung Cancer
Biomarkers
Tumor biomarkers not reported. Severe hyponatremia workup showed high serum osmolality and ethanol level.
Sex
Male
Treatment
chemotherapy, immunotherapy and supportive care
Outcome
Care Ongoing

Treatment course, step by step

  1. Combination chemoimmunotherapy for Stage IIIB non-squamous NSCLC: pemetrexed + pembrolizumab + carboplatin every 3 weeks
  2. recurrent dizziness and severe hyponatremia evaluated during oncology follow-up; workup showed hypertonic hyponatremia due to excess alcohol intake rather than SIADH alone
  3. alcohol detoxification with reducing-dose chlordiazepoxide, vitamin B complex, oral thiamine 50 mg daily, and referral to alcohol cessation support
  4. gradual alcohol reduction and cessation with disappearance of osmolar gap and improvement in serum sodium.

What happened, in summary

This 56-year-old man had Stage IIIB non-squamous non-small-cell lung cancer diagnosed about 1 year before the case presentation. He was receiving combination chemoimmunotherapy with pemetrexed, pembrolizumab, and carboplatin every 3 weeks. His medical history was complex and included dilated cardiomyopathy, coronary artery disease, type 2 diabetes, chronic kidney disease, chronic hepatitis B infection, and prior partial gastrectomy. He smoked 10-12 cigarettes daily and initially said he did not drink much alcohol. Over 3 months, he had 3 episodes of dizziness, each accompanied by severe low serum sodium below 120 mmol/L. He had no headache, seizure, vomiting, diarrhea, excessive thirst, or weight loss. Because lung cancer can be associated with SIADH, that diagnosis was considered, especially because he had a previous episode with low osmolality and urinary findings compatible with mild SIADH. However, the more recent episodes were different: measured serum osmolality was high, and the osmolar gap was markedly elevated at 80 mOsm/kg. Ethanol testing later showed a serum ethanol level of 36 mmol/L, and he then acknowledged daily excess alcohol intake in the preceding months. He was hospitalized for alcohol detoxification with a reducing chlordiazepoxide regimen, vitamin B complex, and oral thiamine. He was referred for alcohol cessation support but preferred self-management. Over 6 months, he gradually stopped alcohol use. His serum ethanol disappeared, the osmolar gap resolved, and sodium levels improved while he continued oncology follow-up. The cancer treatment status remained ongoing, but the dangerous electrolyte abnormality improved once the alcohol-related osmolar gap was recognized and addressed.

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