# Case Report of Acute Severe Hyponatremia Induced by Desmopressin Administration During Chemotherapy

**Authors:** Koutaro Ono, Shugo Uematsu, Aya Yoshihara, Ayako Tsuboya, Shoichi Mori, Takashi Yoshioka, Shuichi Nawata

PMC · DOI: 10.1002/ccr3.72192 · Clinical Case Reports · 2026-03-05

## TL;DR

A 70-year-old man developed severe low sodium levels after resuming a medication called desmopressin during chemotherapy, highlighting the need to carefully manage this drug during cancer treatment.

## Contribution

This case highlights the risk of desmopressin-induced hyponatremia during chemotherapy and advocates for its discontinuation to ensure treatment safety.

## Key findings

- Resuming desmopressin during chemotherapy led to CTCAE Grade 4 hyponatremia.
- Discontinuing desmopressin prevented recurrence of hyponatremia in subsequent chemotherapy cycles.
- The patient completed all planned chemotherapy cycles after desmopressin was stopped.

## Abstract

Patients undergoing chemotherapy are prone to developing hyponatremia due to insufficient oral intake because of nausea and vomiting, administration of large volumes of intravenous fluids, syndrome of inappropriate antidiuretic hormone secretion induced by chemotherapeutic agents, adrenal insufficiency, and drug interactions. Severe hyponatremia during chemotherapy interferes with continuation of cancer treatment. In addition, it may be difficult to distinguish hyponatremia from chemotherapy‐related adverse effects because of symptom similarity. This report presented a case of desmopressin‐induced severe hyponatremia during chemotherapy and discussed the appropriateness of discontinuing desmopressin administration. A 70‐year‐old male was hospitalized for postoperative adjuvant chemotherapy with cisplatin and vinorelbine for a pathological stage IIB adenocarcinoma of the right lower lung lobes. The patient had been taking oral desmopressin (25 μg daily) for 4 years to treat nocturnal polyuria. Desmopressin was discontinued on day 1 of chemotherapy because of a contraindicated combination with dexamethasone, which was administered as an antiemetic. Desmopressin was resumed on day 6, but was followed by Common Terminology Criteria for Adverse Events (CTCAE) Grade 3 nausea, anorexia, and CTCAE Grade 4 hyponatremia (serum sodium concentration of 119 mEq/L) on day 7. Severe hyponatremia progressed following the resumption of desmopressin treatment. Desmopressin was not reintroduced thereafter, and subsequent chemotherapy cycles were continued without recurrence of hyponatremia. The patient completed all four planned adjuvant chemotherapy cycles. This case study highlighted the importance of carefully evaluating the necessity of continuing desmopressin administration and considering its discontinuation during chemotherapy to prevent the onset of hyponatremia.

Resuming desmopressin during chemotherapy can precipitate severe hyponatremia; its necessity should be reassessed and discontinuation considered to ensure safe continuation of cancer treatment.

## Linked entities

- **Chemicals:** cisplatin (PubChem CID 5460033), vinorelbine (PubChem CID 5311497), dexamethasone (PubChem CID 5743), desmopressin (PubChem CID 5311065)
- **Diseases:** adenocarcinoma (MONDO:0004970)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}
- **Diseases:** adenocarcinoma (MESH:D000230), diabetes insipidus (MESH:D003919), adrenal insufficiency (MESH:D000309), cancer (MESH:D009369), diabetes mellitus (MESH:D003920), SIADH (MESH:D007177), Hyponatremia (MESH:D007010), anorexia (MESH:D000855), bronchial asthma (MESH:D001249), nocturnal polyuria (MESH:D011141), RSWS (MESH:D013651), neurological disorders (MESH:D009461), vomiting (MESH:D014839), nausea (MESH:D009325), fatigue (MESH:D005221), myocardial infarction (MESH:D009203), benign prostatic hyperplasia (MESH:D011470), fluid retention (MESH:D016055), hypertension (MESH:D006973), renal dysfunction (MESH:D007674), nausea and vomiting (MESH:D020250), type 2 diabetes mellitus (MESH:D003924), appetite (MESH:D001068), drug allergies (MESH:D004342)
- **Chemicals:** cortisol (MESH:D006854), bilirubin (MESH:D001663), rebamipide (MESH:C052785), platinum (MESH:D010984), linagliptin (MESH:D000069476), omega-3-acid ethyl esters (MESH:C405603), VNR (MESH:D000077235), aspirin (MESH:D001241), palonosetron (MESH:D000077924), Furosemide (MESH:D005665), dexamethasone (MESH:D003907), Cl (MESH:D002713), CDDP (-), Cisplatin (MESH:D002945), thyroxine (MESH:D013974), Na (MESH:D012964), lansoprazole (MESH:D064747), K (MESH:D011188), mirabegron (MESH:C520025), alcohol (MESH:D000438), triiodothyronine (MESH:D014284), mecobalamin (MESH:C019476), metoclopramide (MESH:D008787), Mg (MESH:D008274), azilsartan (MESH:C521273), glucose (MESH:D005947), creatinine (MESH:D003404), pioglitazone (MESH:D000077205), magnesium oxide (MESH:D008277)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12962875/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12962875/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962875/full.md

---
Source: https://tomesphere.com/paper/PMC12962875