“…Whereas earlier efforts were complicated by limited BM reserve and overall poor state of health of patients with advanced HIV disease, as well as synergistic toxicities due to the myelosuppressive effects of zidovudine (15,16), the development of more potent and better tolerated ART regimens with fewer side effects allowed HIV-infected patients with leukemias or lymphomas to receive aggressive antineoplastic therapy, along with autologous or allogeneic HSCT (17)(18)(19)(20)(21). By the end of the first decade of the 2000s, the outcome of autologous HSCT in HIV-infected patients with lymphoma approached that in HIV-uninfected patients (22) and had become a standard of care (22)(23)(24)(25).…”