TY - JOUR
T1 - Characteristics and outcomes of progressive multifocal leukoencephalopathy in hematologic malignancies and stem cell transplant–a case series
AU - Adrianzen Herrera, Diego
AU - Ayyappan, Sabarish
AU - Jasra, Sakshi
AU - Kornblum, Noah
AU - Derman, Olga
AU - Shastri, Aditi
AU - Mantzaris, Ioannis
AU - Verma, Amit
AU - Braunschweig, Ira
AU - Janakiram, Murali
PY - 2019/2
Y1 - 2019/2
N2 - Progressive multifocal leukoencephalopathy (PML) is a life-threatening opportunistic infection of immunomodulatory therapies. PML cases reported in PubMed (1995–2017) following stem-cell transplantation (HSCT) or chemoimmunotherapy (CIT) for hematologic malignancies were reviewed. We found 107 cases, 40% were HSCT recipients (32 allogeneic, 11 autologous) and 40% indolent lymphomas receiving monoclonal antibodies (mAbs). HSCT cases had longer time to PML diagnosis (10.8 vs. 4 months, p <.001), higher proportion of PML therapy response (58% vs. 25%, p =.019), lower mortality rate (56% vs. 88%, p <.001), and longer median survival (8 vs. 2 months, p <.001). Outcome differences might be caused by selection bias as HSCT patients are most likely treated aggressively; however, time-dependent immune reconstitution might also contribute to their better prognosis. Increased use of mAbs and HSCT are associated with rising PML incidence in hematological malignancies, currently constituting the second largest vulnerable population after HIV-infected patients; further research is needed for its optimal treatment.
AB - Progressive multifocal leukoencephalopathy (PML) is a life-threatening opportunistic infection of immunomodulatory therapies. PML cases reported in PubMed (1995–2017) following stem-cell transplantation (HSCT) or chemoimmunotherapy (CIT) for hematologic malignancies were reviewed. We found 107 cases, 40% were HSCT recipients (32 allogeneic, 11 autologous) and 40% indolent lymphomas receiving monoclonal antibodies (mAbs). HSCT cases had longer time to PML diagnosis (10.8 vs. 4 months, p <.001), higher proportion of PML therapy response (58% vs. 25%, p =.019), lower mortality rate (56% vs. 88%, p <.001), and longer median survival (8 vs. 2 months, p <.001). Outcome differences might be caused by selection bias as HSCT patients are most likely treated aggressively; however, time-dependent immune reconstitution might also contribute to their better prognosis. Increased use of mAbs and HSCT are associated with rising PML incidence in hematological malignancies, currently constituting the second largest vulnerable population after HIV-infected patients; further research is needed for its optimal treatment.
KW - Progressive multifocal leukoencephalopathy
KW - hematologic malignancies
KW - monoclonal antibodies
KW - stem cell transplantation
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U2 - 10.1080/10428194.2018.1474523
DO - 10.1080/10428194.2018.1474523
M3 - Article
C2 - 29969336
AN - SCOPUS:85049564267
SN - 1042-8194
VL - 60
SP - 395
EP - 401
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 2
ER -