Impact of the posttransplant lymphoproliferative disorder subtype on survival

Cancer. 2018 Jun 1;124(11):2327-2336. doi: 10.1002/cncr.31339. Epub 2018 Mar 26.

Abstract

Background: Posttransplant lymphoproliferative disorder (PTLD) is a life-threatening complication of solid organ transplantation. Histologic heterogeneity and a lack of treatment standards have made evaluating clinical outcomes in specific patient populations difficult. This systematic literature review investigated the impact of the PTLD histologic subtype on survival in a large data set.

Methods: Case series were identified on PubMed with the search terms post-transplant lymphoproliferative disorder/disease, PTLD, and solid organ transplantation, with additional publications identified through reference lists. The patient characteristics, immunosuppressive regimen, treatment, survival, and follow-up time for 306 cases were extracted from 94 articles, and these cases were combined with 11 cases from Emory University Hospital. Patients with a recorded subtype were included in a Kaplan-Meier survival analysis (n = 234). Cox proportional hazards regression analyses identified predictors of overall survival (OS) for each subtype and B-cell subgroup.

Results: OS differed significantly between monomorphic T-cell neoplasms (median, 9 months) and polymorphic, monomorphic B-cell, and Hodgkin-type neoplasms, for which the median OS was not reached (P = .0001). Significant differences in OS among B subgroups were not detected, but there was a trend toward decreased survival for patients with Burkitt-type PTLD. Kidney transplantation and a reduction of immunosuppression were associated with increased OS for patients with B-cell neoplasms in a multivariate analysis. Immunosuppression with azathioprine was associated with decreased OS for patients with T-cell neoplasms, whereas radiotherapy was associated with improved OS for patients with that subtype.

Conclusions: The histologic subtype represents an important prognostic factor in PTLD, with patients with T-cell neoplasms exhibiting very poor OS. Possibly lower survival for certain subsets of patients with B-cell PTLD should be explored further and suggests the need for subtype-specific therapies to improve outcomes. Cancer 2018;124:2327-36. © 2018 American Cancer Society.

Keywords: B-cell neoplasms; T-cell neoplasms; immunosuppression; posttransplant lymphoproliferative disorder; survival.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Antineoplastic Agents, Immunological / therapeutic use
  • Chemoradiotherapy / methods
  • Graft Rejection / immunology
  • Graft Rejection / prevention & control
  • Humans
  • Immunocompromised Host / drug effects
  • Immunocompromised Host / immunology
  • Immunosuppression Therapy / adverse effects*
  • Immunosuppression Therapy / methods
  • Immunosuppressive Agents / adverse effects
  • Incidence
  • Kaplan-Meier Estimate
  • Lymphoproliferative Disorders / immunology
  • Lymphoproliferative Disorders / mortality*
  • Lymphoproliferative Disorders / therapy
  • Organ Transplantation / adverse effects*
  • Postoperative Complications / etiology
  • Postoperative Complications / mortality*
  • Progression-Free Survival
  • Risk Factors

Substances

  • Antineoplastic Agents, Immunological
  • Immunosuppressive Agents