van Rhee F, Lin F, Cullis J O, Spencer A, Cross N C, Chase A, Garicochea B, Bungey J, Barrett J, Goldman J M
Leukaemia Research Fund Centre for Adult Leukaemia, Royal Postgraduate Medical School, London, UK.
Blood. 1994 Jun 1;83(11):3377-83.
Fourteen patients with chronic myeloid leukemia (CML) relapsing after allogeneic bone marrow transplant (BMT) were treated with leukocyte transfusions from the original marrow donor (sibling, n = 9; volunteer unrelated, n = 5). The relapse was defined at the molecular level in two cases, cytogenetically in five cases and hematologically in seven cases. Ten patients responded, seven of seven patients with cytogenetic/molecular relapse compared with three of seven with hematologic relapse (P < .03). All five recipients of cells from unrelated donors responded. Eight of the 10 responders have achieved polymerase chain reaction-negative status and this persisted in three patients for more than 2 years; no responder has shown sign of relapse. Reversible marrow aplasia occurred in two patients, both treated in hematologic relapse. Severe graft-versus-host disease occurred in four patients and was fatal in one. We confirm previous reports that donor leukocyte transfusions are effective in the management of CML in relapse after BMT. In this series, therapeutic intervention before the onset of hematologic relapse was associated with an increased likelihood of response and no marrow aplasia.
14例异基因骨髓移植(BMT)后复发的慢性髓性白血病(CML)患者接受了来自原骨髓供者(同胞,n = 9;志愿非亲属,n = 5)的白细胞输注。2例复发在分子水平定义,5例在细胞遗传学水平定义,7例在血液学水平定义。10例患者有反应,细胞遗传学/分子复发的7例患者中有7例有反应,而血液学复发的7例患者中有3例有反应(P <.03)。所有5例接受非亲属供者细胞的受者均有反应。10例有反应者中有8例达到聚合酶链反应阴性状态,其中3例持续超过2年;无反应者出现复发迹象。2例患者发生可逆性骨髓再生障碍,均在血液学复发时接受治疗。4例患者发生严重移植物抗宿主病,1例死亡。我们证实了先前的报道,即供者白细胞输注对BMT后复发的CML治疗有效。在本系列中,在血液学复发发生前进行治疗干预与反应可能性增加及无骨髓再生障碍相关。