We just recently have had a patient (Indian) who was admitted with pulmonary infiltrates. He has a history of Hodgkins disease and was treated with ABVD (adriamycin, bleomycin, vincristine and decadron). Though no definitive diagnosis has been made, bleomycin pulmonary toxicity is considered a high in the list of differential (and most likely).
The interesting observation is that this is a second male from India who has been admitted with similar presentation and diagnosed with bleomycin pulmonary toxicity.
Why is this important? At least in the oncology world --- one of the frontiers is selecting dosing for drugs based on specific mutations. Is there a specific genetic mutation that makes these patients more susceptible to pulmonary toxicities? Are there specific mutations that might suggest better response?
I only
have specific information on the currently admitted patient, but not the other patient.
Thoughts?
Biren