Comprehensive Guide for Oxaliplatin: Infusion and Hypersensitivity Reactions
Infusion Reaction Management
Comprehensive Guide for Oxaliplatin: Infusion and Hypersensitivity Reactions
Oxaliplatin is a third-generation platinum-based chemotherapeutic agent widely used in colorectal cancer and other gastrointestinal malignancies. While generally well-tolerated, infusion and hypersensitivity reactions (HSRs) can occur and require vigilant monitoring.
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1. Incidence Rate of Infusion or Hypersensitivity Reactions
- Overall incidence of hypersensitivity reactions (HSRs) to oxaliplatin: ranges from 2% to 25% depending on cumulative exposure and patient population.
- Grade 3–4 severe reactions: occur in approximately 1.6%–2.3% of patients.
- Timing: HSRs typically occur after multiple treatment cycles — most commonly after the 6th cycle or later — due to repeated antigen exposure and sensitization.
2. Onset, Signs, and Symptoms of Reactions
Onset:
- Most infusion-related reactions (IRRs) occur during the infusion or within minutes to hours following administration.
- Immediate reactions: usually within the first 30 minutes of infusion.
- Delayed reactions: can occur up to several hours after infusion.
Signs and Symptoms:
- Mild to Moderate (Grade 1–2):
- Flushing
- Rash, pruritus
- Urticaria
- Mild hypotension or hypertension
- Fever and chills
- Dyspnea without bronchospasm
- Severe (Grade 3–4):
- Bronchospasm, chest tightness
- Laryngeal edema, throat tightness
- Anaphylaxis (with hypotension, tachycardia, generalized urticaria, collapse)
- Severe hypotension or shock
3. Prophylactic Medications (Given 30–60 minutes prior to infusion)
Although routine premedication is not universally required for all first-time oxaliplatin recipients, prophylactic regimens are recommended in patients at higher risk or with prior mild reactions, or when continuing therapy after desensitization.Common prophylactic options:
- Corticosteroids:
- Dexamethasone 8–20 mg IV (commonly given as part of the antiemetic regimen)
- H1 Antihistamines:
- Diphenhydramine 25–50 mg IV
- or Cetirizine 10 mg orally (less sedating option; may be given prior to arrival)
- H2 Antagonists:
- Ranitidine 50 mg IV
- or Famotidine 20 mg IV
- Optional (especially with prior reactions):
- Acetaminophen 650 mg orally to reduce fever/chills risk
4. Management Strategies for Infusion Reactions Specific to Oxaliplatin
A. If Reaction Occurs During Infusion:
- Immediately stop the infusion; maintain IV access.
- Assess airway, breathing, circulation (ABCs).
- Administer oxygen and monitor vital signs closely.
- Pharmacologic interventions:
- Epinephrine (0.3–0.5 mg IM, 1:1000 concentration) for anaphylaxis.
- Antihistamines: diphenhydramine 25–50 mg IV.
- Corticosteroids: dexamethasone or methylprednisolone IV bolus.
- H2 antagonists: famotidine or ranitidine IV.
- Bronchodilators for bronchospasm (e.g., albuterol via nebulizer).
- IV fluids for hypotension and shock.
- If symptoms resolve, discuss risk/benefit of rechallenge versus discontinuation.
B. Rechallenge Protocols (for mild/moderate reactions):
- May be considered in selected patients after risk assessment.
- Slower infusion rate (e.g., extend to 6 hours or more).
- Escalating dose desensitization protocols under close supervision in specialized centers.
- Premedication with steroid + H1/H2 antihistamines before subsequent doses.
C. Discontinuation Criteria:
- Grade 3–4 life-threatening reactions or confirmed anaphylaxis are generally considered absolute indications to permanently discontinue oxaliplatin.
Key Monitoring Recommendations
- First 15–30 min of infusion: highest vigilance.
- Have emergency resuscitation drugs and equipment readily available.
- Educate patients to report symptoms immediately — even subtle sensations (throat tightness, itching, chest pressure).
Oxaliplatin Hypersensitivity Reaction Management Flowchart
https://info.pharkeep.com/oxaliplatin-reaction.html

References
- Andre T, Boni C, Mounedji-Boudiaf L, et al. N Engl J Med. 2004;350(23):2343–2351.
- Maindrault-Goebel F, et al. “Allergic-type reactions to oxaliplatin: retrospective analysis.” Eur J Cancer. 2005;41(15):2262-2267.
- Markman M. “Toxicities of the platinum antineoplastic agents.” UptoDate. Last updated 2023.
- Shimada Y, et al. Cancer Chemother Pharmacol. 2009;64:587–593.