Prognostic factors in patients with post-transplant lymphoproliferative disorders (PTLD) in the rituximab era

被引:64
|
作者
Ghobrial, IM
Habermann, TM
Ristow, KM
Ansell, SM
Macon, W
Geyer, SM
McG egor, CG
机构
[1] Mayo Fdn, Mayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Cardiovasc Surg, Rochester, MN USA
[3] Mayo Clin, Dept Pathol, Rochester, MN USA
[4] Mayo Clin, Dept Biostat, Rochester, MN USA
关键词
PTLD; rituximab; prognostic factors;
D O I
10.1080/10428190400012011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To assess the effect of rituximab therapy and other prognostic factors on overall survival in patients with post-transplant lymphoproliferative disorders (PTLD) after solid organ transplantation, 30 consecutive patients diagnosed with PTLD between 1999 and 2002 were analyzed. Fifteen (50%) patients received rituximab (375 mg/m(2) once a week). Fifteen ( 50%) patients had other interventions including observation, immunosuppression reduction, surgery, chemotherapy, radiation or a combination of these. Patients receiving rituximab vs. non-rituximab differed in the following variables: age at diagnosis of PTLD (P=0.009), days to PTLD (P=0.0005), Epstein-Barr virus (EBV) in situ hybridization status (P=0.02) and CD20-positive status (P=0.006). At the time of last follow-up, 10 (33%) patients in the rituximab group and 5 (17%) in the nonrituximab group were alive. On univariate analysis for overall survival of all 30 patients, the significant factors were: treatment with rituximab (P=0.03), response to treatment (P=0.005), CD20 positive (P=0.0004), low international prognostic index (IPI; P = 0.02) and good performance status (P = 0.009). Multivariate analysis of all patients was significant for CD20-positive status (P=0.0007) and low performance status (P=0.006). On multivariate analysis for overall survival in patients with CD20-positive PTLD, low IPI (P=0.004) and rituximab therapy (P=0.03) were significant. Low IPI and rituximab therapy led to an improved overall survival in patients with CD20-positive PTLD.
引用
收藏
页码:191 / 196
页数:6
相关论文
共 50 条
  • [21] First-line treatment with rituximab improves survival of patients with post-transplant lymphoproliferative disease (PTLD).
    Gonzalez-Barca, E
    Domingo-Domenech, E
    Gomez-Codina, J
    Capote, F
    Flores, E
    Briones, J
    Salar, A
    Panizo, C
    Montalban, C
    Ribera, JM
    Caballero, D
    Muñoz, A
    Gallur, L
    Canales, MA
    Fernandez, P
    Encuentra, M
    de Sevilla, AF
    BLOOD, 2004, 104 (11) : 394A - 394A
  • [22] Outcomes and prognostic factors for adult patients with Post-Transplant Lymphoproliferative Disorders: the Thames Valley experience
    Barbanti, Maria Chiara
    Burton, Kieran
    Fordwor, Katrina
    Pervaiz, Omer
    Sangha, Gavinda
    Stanton, Louise
    Collins, Graham
    BRITISH JOURNAL OF HAEMATOLOGY, 2022, 197 : 107 - 108
  • [23] Treatment of post-transplant lymphoproliferative disorder (PTLD) with rituximab or chemotherapy: The University of Pennsylvania experience
    Elstrom, RL
    Andreadis, C
    Aqui, N
    Tsai, DE
    BLOOD, 2005, 106 (11) : 275A - 275A
  • [24] Who is at risk for post-transplant lymphoproliferative disorders (PTLD) after liver transplantation?
    Aucejo, F
    Rofaiel, G
    Miller, C
    JOURNAL OF HEPATOLOGY, 2006, 44 (01) : 19 - 23
  • [25] Post-transplant lymphoproliferative disorders (PTLD): Outcome of therapy with interferon alfa (IFN).
    Morrison, VA
    Dunn, DL
    Shapiro, RS
    Peterson, BA
    BLOOD, 1996, 88 (10) : 3498 - 3498
  • [26] A new technique for establishing and tracking clonality in post-transplant lymphoproliferative disorders (PTLD)
    Neppalli, V
    Coad, JE
    Brown, CA
    MODERN PATHOLOGY, 2002, 15 (01) : 343A - 343A
  • [27] The role of immunologic effector cells in the development of post-transplant lymphoproliferative disorders (PTLD).
    Shpilberg, O
    Wilson, J
    Green, M
    Nalesnik, M
    Day, R
    Herberman, RB
    Whiteside, T
    BLOOD, 1995, 86 (10) : 1354 - 1354
  • [28] Morphologic Evolution in Post-Transplant Lymphoproliferative Disorders (PTLD): A Clinicopathologic Case Series
    Stubbins, Ryan J.
    Peters, Anthea C.
    Curtis, Mabilang
    Owen, Carolyn
    Mansoor, Adnan
    Lai, Raymond
    Preiksaitis, Jutta
    BLOOD, 2015, 126 (23)
  • [29] A new technique for establishing and tracking clonality in post-transplant lymphoproliferative disorders (PTLD)
    Neppalli, V
    Coad, JE
    Brown, CA
    LABORATORY INVESTIGATION, 2002, 82 (01) : 343A - 343A
  • [30] Classic Hodgkin lymphoma post-transplant lymphoproliferative disorders (PTLD) are often preceded by discordant PTLD subtypes
    Stubbins, Ryan J.
    Mabilangan, Curtis
    Rojas-Vasquez, Marta
    Lai, Raymond L.
    Zhu, James
    Preiksaitis, Jutta P.
    Peters, Anthea C.
    LEUKEMIA & LYMPHOMA, 2020, 61 (14) : 3319 - 3330