Mackinnon S, Barnett L, Heller G
Bone Marrow Transplant Service Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.
Bone Marrow Transplant. 1996 Apr;17(4):643-7.
In chronic myeloid leukemia (CML) the polymerase chain reaction (PCR) can be used to detect minimal residual disease after bone marrow transplantation (BMT). Previous studies have shown that PCR positivity is common following BMT. However, the clinical significance of this finding for any given individual who is PCR positive remains unclear, as many of these patients remain long-term disease-free survivors after allogeneic BMT. In the present study, we used PCR to detect BCR-ABL mRNA in 144 blood or marrow samples from 36 patients who received a T cell-depleted BMT for CML in first chronic phase. Six patients had no evidence of PCR-detectable residual disease at any time following transplant. The other 30 patients had at least one positive PCR result post-BMT. Once PCR positivity was found, it was usually sustained, with only four patients having a subsequent PCR negative assay. No patient who had two consecutive PCR-positive assays had a return to PCR negativity. None of the six patients with exclusively PCR-negative assays have developed either cytogenetic or hematologic relapse at a median follow-up of 42 months. Of the 30 patients with at least one PCR-positive assay post-BMT, 28 were PCR positive at last follow-up, and 22 have progressed to cytogenetic or hematologic relapse. If the PCR-positive assay occurred within 24 months of the transplant then the estimated probability of progression to cytogenetic or hematologic relapse was 65% at 24 months. Twenty of the 26 patients who were studied early (< or = 6 months) after BMT had at least one positive PCR assay. Fifteen of the 20 patients who were PCR positive < or = 6 months following transplant have progressed to either cytogenetic or hematologic relapse resulting in an estimated probability of relapse of 84% at 24 months. These results indicate that following T cell-depleted BMT for CML in first chronic phase, PCR is highly predictive of relapse and may identify a cohort of patients in need of therapeutic intervention before the onset of overt clinical relapse.
在慢性粒细胞白血病(CML)中,聚合酶链反应(PCR)可用于检测骨髓移植(BMT)后的微小残留病。先前的研究表明,BMT后PCR阳性很常见。然而,对于任何PCR阳性的个体而言,这一发现的临床意义仍不明确,因为许多此类患者在异基因BMT后仍是长期无病生存者。在本研究中,我们使用PCR检测了36例处于慢性期的CML患者接受T细胞去除的BMT后144份血液或骨髓样本中的BCR-ABL mRNA。6例患者在移植后的任何时间均无PCR可检测到的残留病证据。其他30例患者在BMT后至少有一次PCR结果为阳性。一旦发现PCR阳性,通常会持续存在,只有4例患者随后PCR检测为阴性。连续两次PCR检测为阳性的患者均未恢复为PCR阴性。在中位随访42个月时,6例PCR检测始终为阴性的患者均未发生细胞遗传学或血液学复发。在30例BMT后至少有一次PCR检测为阳性的患者中,28例在最后一次随访时PCR仍为阳性,22例已进展为细胞遗传学或血液学复发。如果PCR阳性检测发生在移植后24个月内,那么在24个月时进展为细胞遗传学或血液学复发的估计概率为65%。在BMT后早期(≤6个月)接受研究的26例患者中,20例至少有一次PCR检测为阳性。移植后PCR阳性≤6个月的20例患者中有15例已进展为细胞遗传学或血液学复发,导致在24个月时复发的估计概率为84%。这些结果表明,对于处于慢性期的CML患者进行T细胞去除的BMT后,PCR对复发具有高度预测性,并且可能在明显临床复发发生之前识别出一批需要进行治疗干预的患者。