Clinical features of late cytomegalovirus infection after hematopoietic stem cell transplantation

被引:45
作者
Asano-Mori, Yuki [1 ,2 ]
Kanda, Yoshinobu [1 ]
Oshima, Kumi [1 ]
Kako, Shinichi [1 ]
Shinohara, Akihito [1 ]
Nakasone, Hideki [1 ]
Sato, Hiroyuki [1 ]
Watanabe, Takuro [1 ]
Hosoya, Noriko [3 ]
Izutsu, Koji [1 ]
Asai, Takashi [1 ]
Hangaishi, Akira [1 ]
Motokura, Toru [1 ]
Chiba, Shigeru [3 ]
Kurokawa, Mineo [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Japanese Red Cross Med Ctr, Dept Hematol, Tokyo, Japan
[3] Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Tokyo 113, Japan
关键词
cytomegalovirus; antigenemia; ganciclovir; preemptive therapy; hematopoietic stem cell transplantation;
D O I
10.1007/s12185-008-0051-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Late cytomegalovirus (CMV) disease beyond day 100 after hematopoietic stem cell transplantation (HSCT) has become an increasing problem after the introduction of preemptive ganciclovir (GCV) administration. To clarify the risk factors and outcome for late CMV reactivation and disease, we retrospectively analyzed the records of 101 Japanese adult patients who underwent allogeneic HSCT between 1998 and 2005 at our hospital. Fifty-one developed late positive CMV antigenemia, with a cumulative incidence of 53%. Recipient CMV seropositivity, the use of alemtuzumab, chronic GVHD, and high-dose steroids were significantly associated with late positive antigenemia. Eight patients developed late CMV disease, with a cumulative incidence of 8%, including retinitis and gastrointestinal disease. None progressed to a fatal disease. The use of alemtuzumab was identified as an independent significant risk factor for late CMV disease, although it was not associated with increased non-relapse mortality. Among the 51 patients with late positive antigenemia, 28 had consistently less than three positive cells, 25 of whom showed negative conversion without antiviral agents. In conclusion, late CMV antigenemia appeared to develop frequently, especially in patients with profound immune suppression; however, a fatal outcome could be prevented by optimal preemptive therapy. Low-level antigenemia may not require antiviral treatments.
引用
收藏
页码:310 / 318
页数:9
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