What is the management of Bleomycin-induced lung fibrosis?

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Last updated: October 17, 2025View editorial policy

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Management of Bleomycin-Induced Lung Fibrosis

The management of bleomycin-induced lung fibrosis requires immediate cessation of bleomycin therapy, administration of oral corticosteroids (prednisolone 0.5 mg/kg for 7 days with subsequent tapering), and referral to a respiratory physician with expertise in interstitial lung disease. 1

Diagnosis and Assessment

  • Diagnosis is made by combining systemic symptoms (particularly dry cough and shortness of breath) with typical radiological changes on high-resolution computed tomography (HRCT) 1
  • Cough is the most sensitive symptom for predicting bleomycin-induced pulmonary toxicity and should trigger immediate investigation 1
  • HRCT is the investigation of choice for suspected bleomycin-induced lung toxicity, as chest X-ray has extremely low sensitivity 1
  • Pulmonary function tests (PFTs) provide supportive evidence but are not diagnostic on their own; diffusion capacity for carbon monoxide (DLCO) is the most significant parameter 1, 2

Acute Management

  • Immediate discontinuation of bleomycin therapy when pulmonary toxicity is suspected or confirmed 1, 2
  • Oral prednisolone at 0.5 mg/kg for 7 days with subsequent tapering is recommended for all CT-confirmed diagnoses of bleomycin lung toxicity 1
  • Low threshold for antimicrobial therapy as infection can mimic, coexist with, and drive the development of fibrosis 1
  • Referral to or discussion with a respiratory physician with expertise in interstitial lung disease is strongly recommended in cases of confirmed toxicity 1

Monitoring and Follow-up

  • All patients receiving more than 300 units of bleomycin should receive a post-treatment CT scan 1
  • Further investigations should be symptom-led, with particular attention to new or worsening cough or dyspnea 1
  • Monthly monitoring of DLCO is recommended if it is employed to detect subclinical pulmonary toxicity; discontinue bleomycin when DLCO falls below 30-35% of the pretreatment value 2
  • Long-term follow-up is essential as lung fibrosis may develop or progress years after cessation of bleomycin therapy 3

Special Considerations

  • Avoid high oxygen concentrations in patients with a history of bleomycin treatment, as this can trigger or exacerbate pulmonary fibrosis 2, 4
  • For patients requiring surgery after bleomycin therapy, maintain FIO₂ at concentrations approximating room air (25%) during surgery and the postoperative period 2
  • Monitor fluid replacement carefully, focusing more on colloid administration rather than crystalloid 2
  • Patients over 40 years of age, those with renal dysfunction, significant smoking history, and pre-existing lung disease are at higher risk for developing bleomycin-induced pulmonary fibrosis 1, 5

Experimental Approaches

  • MRTF/SRF pathway inhibitors have shown promise in preventing bleomycin-induced lung fibrosis in preclinical studies 6
  • Adenovirus-mediated gene transfer of bleomycin resistance genes has demonstrated potential in preventing bleomycin-induced pulmonary fibrosis in animal models 7

Patient Education

  • Every patient receiving bleomycin should receive a post-treatment advice sheet regarding potential pulmonary complications 1
  • Patients should be instructed to report new respiratory symptoms promptly, particularly cough and dyspnea 1
  • Patients should inform all healthcare providers about their history of bleomycin treatment, especially before procedures requiring oxygen administration 2, 4

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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