Plasma Cell Neoplasms in US Solid Organ Transplant Recipients

被引:29
作者
Engels, Eric A. [1 ]
Clarke, Christina A. [2 ]
Pfeiffer, Ruth M. [1 ]
Lynch, Charles F. [3 ]
Weisenburger, Dennis D. [4 ]
Gibson, Todd M. [1 ]
Landgren, Ola [5 ]
Morton, Lindsay M. [1 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, Rockville, MD USA
[2] Canc Prevent Inst Calif, Fremont, CA USA
[3] Univ Iowa, Iowa City, IA USA
[4] City Hope Natl Med Ctr, Duarte, CA USA
[5] NCI, Ctr Canc Res, Bethesda, MD 20892 USA
关键词
Epstein-Barr virus; immunosuppression; multiple myeloma; plasmacytoma; primary biliary cirrhosis; posttransplant lymphoproliferative disorder; PRIMARY BILIARY-CIRRHOSIS; POSTTRANSPLANT LYMPHOPROLIFERATIVE DISORDER; EPSTEIN-BARR-VIRUS; STAGE RENAL-DISEASE; MULTIPLE-MYELOMA; CANCER INCIDENCE; EXTRAMEDULLARY PLASMACYTOMA; UNDETERMINED SIGNIFICANCE; KIDNEY-TRANSPLANTATION; LIVER-TRANSPLANTATION;
D O I
10.1111/ajt.12234
中图分类号
R61 [外科手术学];
学科分类号
摘要
Transplant recipients have elevated risk for plasma cell neoplasms (PCNs, comprising multiple myeloma and plasmacytoma), but little is known about risk factors in the transplant setting. Through linkage of the US solid organ transplant registry with 15 state/regional cancer registries, we identified 140 PCNs in 202600 recipients (1987-2009). PCN risk was 1.8-fold increased relative to the general population (standardized incidence ratio [SIR] 1.80, 95%CI 1.51-2.12). Among cases, 102 were multiple myeloma (SIR 1.41) and 38 were plasmacytoma (SIR 7.06). PCN incidence increased with age, but due to the rarity of PCNs in younger people in the general population, SIRs were highest in younger transplant recipients (p=0.03). PCN risk was especially high in recipients who were Epstein-Barr virus (EBV) seronegative at transplantation (SIR 3.93). EBV status was known for 18 tumors, of which 7 (39%) were EBV positive. Following liver transplantation, PCN risk was higher in recipients with cholestatic liver disease (SIR 2.78); five of these cases had primary biliary cirrhosis (PBC). A role for primary EBV infection after transplantation is supported by the increased PCN risk in young EBV seronegative recipients and the presence of EBV in tumors. PBC may be another risk factor, perhaps by causing chronic immune activation.
引用
收藏
页码:1523 / 1532
页数:10
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