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数字PCR定量检测ALK阳性间变性大细胞淋巴瘤微小病变:迈向国际试验风险分层的一步?

Quantification of Minimal Disease by Digital PCR in ALK-Positive Anaplastic Large Cell Lymphoma: A Step towards Risk Stratification in International Trials?

作者信息

Damm-Welk Christine, Lovisa Federica, Contarini Giorgia, Lüdersen Jette, Carraro Elisa, Knörr Fabian, Förster Jan, Zimmermann Martin, Sala Alessandra, Vinti Luciana, Tondo Annalisa, Pillon Marta, Woessmann Wilhelm, Mussolin Lara

机构信息

Pediatric Hematology and Oncology, University Medical Center Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Maternal and Child Health Department, Padova University, 35128 Padova, Italy.

出版信息

Cancers (Basel). 2022 Mar 27;14(7):1703. doi: 10.3390/cancers14071703.

Abstract

Minimal disseminated and residual disease (MDD/MRD) analyzed by qualitative PCR for NPM-ALK fusion transcripts are validated prognostic factors in pediatric ALK-positive anaplastic large cell lymphoma (ALCL). Although potentially promising, MDD quantification by quantitative real-time PCR in international trials is technically challenging. Quantification of early MRD might further improve risk stratification. We aimed to assess droplet digital PCR for quantification of minimal disease in an inter-laboratory setting in a large cohort of 208 uniformly treated ALCL patients. Inter-laboratory quality control showed high concordance. Using a previously described cut-off of 30 copies NPM-ALK/104 copies ABL1 (NCN) in bone marrow and peripheral blood, MDD quantification allowed identification of very high-risk patients (5-year PFS% 34 ± 5 for patients with ≥30 NCN compared to 74 ± 6 and 76 ± 5 for patients with negative or <30 NCN, respectively, p < 0.0001). While MRD positivity was confirmed as a prognostic marker for the detection of very high-risk patients in this large study, quantification of MRD fusion transcripts did not improve stratification. PFS% was 80 ± 5 and 73 ± 6 for MDD- and MRD-negative patients, respectively, versus 35 ± 10 and 16 ± 8 for MRD-positive patients with <30 and ≥30 NCN, p < 0.0001. Our results suggest that MDD quantification by dPCR enables improved patient stratification in international clinical studies and patient selection for early clinical trials already at diagnosis.

摘要

通过定性PCR分析NPM-ALK融合转录本检测的微小播散和残留病(MDD/MRD)是儿童ALK阳性间变性大细胞淋巴瘤(ALCL)中经过验证的预后因素。尽管具有潜在前景,但在国际试验中通过定量实时PCR对MDD进行定量在技术上具有挑战性。早期MRD的定量可能会进一步改善风险分层。我们旨在评估在一大群208例接受统一治疗的ALCL患者的实验室间环境中,使用液滴数字PCR对微小疾病进行定量。实验室间质量控制显示出高度一致性。使用先前描述的骨髓和外周血中30拷贝NPM-ALK/104拷贝ABL1(NCN)的临界值,MDD定量能够识别出极高风险患者(≥30 NCN的患者5年无进展生存率为34±5%,而NCN阴性或<30 NCN的患者分别为74±6%和76±5%,p<0.0001)。虽然在这项大型研究中MRD阳性被确认为检测极高风险患者的预后标志物,但MRD融合转录本的定量并未改善分层。MDD阴性和MRD阴性患者的无进展生存率分别为80±5%和73±6%,而NCN<30和≥30的MRD阳性患者分别为35±10%和16±8%,p<0.0001。我们的结果表明,通过数字PCR进行MDD定量能够在国际临床研究中改善患者分层,并在诊断时为早期临床试验进行患者选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2fb/8996924/23449c0a52a3/cancers-14-01703-g001.jpg

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