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Persistence of dormant leukemic progenitors during interferon-induced remission in chronic myelogenous leukemia. Analysis by polymerase chain reaction of individual colonies.

机译:在慢性粒细胞性白血病的干扰素诱导的缓解期间休眠的白血病祖细胞的持久性。通过聚合酶链反应分析单个菌落。

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摘要

Interferon-alpha induces durable cytogenetic remissions in about one-quarter of newly diagnosed patients with chronic myelogenous leukemia (CML). Even so, after short-term follow-up, previous studies have shown that residual leukemic cells can be detected by the polymerase chain reaction (PCR) in all of these individuals. The objectives of our study were therefore to obtain long-term follow-up data on residual disease in a cohort of complete responders and to determine if leukemic cells with clonogenic potential are present in patients despite the absence of relapse. We performed (a) serial analysis of blood and/or bone marrow for a reverse transcriptase PCR amplified BCR-ABL transcript at times well beyond the point that cytogenetic remission was first attained and (b) reverse transcriptase PCR of individually plucked myeloid and erythroid colonies for the presence of the same transcript. Seven CML patients who had previously attained complete cytogenetic remission while on interferon-alpha were investigated. Six of the seven patients were in complete cytogenetic remission at the time of analysis, whereas one patient had early evidence of cytogenetic relapse. With ongoing therapy, five patients with the longest follow-up eventually achieved PCR negativity at time periods of 27, 32, 36, 49, and 67 mo after a complete cytogenetic remission was first noted. Even so, residual disease was detected in progenitor cells derived from two patients, each of whom had been in continuous cytogenetic remission for approximately 2.5 and 3.5 yr, respectively. Progenitors expressing BCR-ABL transcripts were also detected in the patient with early cytogenetic relapse. These observations demonstrate that residual disease resides in colony-forming cells that should have the potential to repopulate the bone marrow. However, the presence of a minority of Ph-positive CML progenitor cells for a very long period of time is still compatible with durable remission, confirming that a situation of tumor dormancy may be induced in CML by interferon therapy.
机译:干扰素-α在大约四分之一的新诊断的慢性粒细胞性白血病(CML)患者中诱导持久的细胞遗传学缓解。即使这样,在短期随访之后,先前的研究表明,通过所有这些个体中的聚合酶链反应(PCR)可以检测到残留的白血病细胞。因此,我们的研究目的是获得一组完全反应者中残留疾病的长期随访数据,并确定尽管没有复发,患者中是否仍存在具有克隆形成潜能的白血病细胞。我们进行了(a)血液和/或骨髓的系列分析,其逆转录酶PCR扩增的BCR-ABL转录本的时间远远超过首次获得细胞遗传学缓解的时间,以及(b)分别摘除的髓样和红系集落的逆转录酶PCR存在相同的成绩单。研究了七名先前接受干扰素α治疗时已经达到完全细胞遗传学缓解的CML患者。在分析时,七名患者中有六名完全细胞遗传学缓解,而一名患者早期有细胞遗传学复发的证据。在进行中的治疗中,随访时间最长的五名患者在首次观察到完全的细胞遗传学缓解后最终在27、32、36、49和67 mo时达到了PCR阴性。即便如此,在两名患者的祖细胞中仍检测到残留疾病,每名患者分别持续持续约2.5年和3.5年的细胞遗传学缓解。在具有早期细胞遗传学复发的患者中也检测到表达BCR-ABL转录本的祖细胞。这些观察结果表明,残留的疾病存在于集落形成细胞中,该细胞应具有重新聚集骨髓的潜力。然而,在很长一段时间内少数Ph阳性CML祖细胞的存在仍与持久缓解相容,这证实了通过干扰素治疗可在CML中诱发肿瘤休眠的情况。

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