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Acute immune-therapy toxicity

Essential points for quick revision.

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Immune-mediated organ failure, CRS or ICANS

Hypoxia, shock, chest pain, arrhythmia, severe diarrhoea, jaundice, adrenal crisis, weakness, confusion, aphasia, seizure or reduced consciousness during or after immune therapy can deteriorate rapidly.

Action: Use ABCDE care, hold further immune therapy, call acute oncology and the treating centre, investigate and treat sepsis concurrently, obtain organ-directed tests and start protocol corticosteroid, hormone replacement, tocilizumab or other rescue according to the toxicity syndrome and grade.

Synopsis

Recognise life-threatening checkpoint-inhibitor, CAR-T and bispecific-antibody toxicity, treat infection and other mimics in parallel and start severity- and organ-specific immune rescue without waiting for routine oncology review.

  • Immune toxicity can affect any organ and may begin during treatment or weeks to months after the last checkpoint dose; ask specifically about the exact immune product and date.
  • Withhold further immune therapy for clinically significant suspected toxicity and contact acute oncology or the cellular-therapy centre immediately.
  • First-line assessment combines ABCDE, sepsis cultures and lactate, FBC, renal, liver, glucose, cortisol and thyroid tests with organ-specific ECG, troponin, CT, stool or neurological evaluation.

Key red flags

New breathlessness, hypoxaemia or diffuse lung change during checkpoint therapy may be pneumonitis, infection or embolism and requires urgent imaging and oncology review.

Immune colitis

Increasing stool frequency, nocturnal diarrhoea, blood, pain or fever can progress to dehydration, toxic dilatation and perforation.

Investigation priorities

01
First-line sepsis and organ screenFirst stepFirst line

Identify infection, shock and the organ systems requiring immediate support.

Management branches

InitialHold therapy and assess both toxicity and infection

A patient exposed to immune therapy develops a new inflammatory, endocrine, cardiac or neurological syndrome.

  1. Use ABCDE and monitoring, identify exact product and dates, hold further immune treatment and contact acute oncology or the cellular-therapy centre immediately.
  2. Obtain sepsis and organ-directed tests and start antimicrobials and other emergency treatment when indicated without waiting for a toxicity grade.

Key medicines

Intravenous methylprednisolone for severe checkpoint toxicityGive methylprednisolone 1 to 2 mg/kg intravenously once daily, or the divided organ-specific equivalent, for severe immune-mediated toxicity, with pulse dosing reserved for selected life-threatening cardiac or neurological disease under specialist protocol.
Hydrocortisone for adrenal crisisGive hydrocortisone 100 mg intravenously or intramuscularly immediately, then 200 mg over 24 hours by infusion or 50 mg intravenously every 6 hours with intravenous 0.9% sodium chloride and glucose as required.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom