“…Other early clinical data confirmed an increased lymphoma incidence with AZA, even after short-term use (59). In addition to the increased risk for lymphomas, AZA has also been correlated with induction of a broad variety of solid neoplasms, including squamous cell carcinoma (60,61), urinary bladder tumors (62), breast cancer (63), and brain tumors (64). However, with the more recent use of new combined immunosuppressive regimens, the effects of less intensive use of AZA on tumor development in a transplant situation become difficult to assess.…”