Cristiano Antonio, Palmieri Raffaele, Fabiani Emiliano, Ottone Tiziana, Divona Mariadomenica, Savi Arianna, Buccisano Francesco, Maurillo Luca, Tarella Corrado, Arcese William, Voso Maria Teresa
Department of Biomedicine and Prevention, University of Rome "Tor Vergata," Rome, Italy.
UniCamillus-Saint Camillus International University of Health Sciences, Rome, Italy.
Mediterr J Hematol Infect Dis. 2022 May 1;14(1):e2022041. doi: 10.4084/MJHID.2022.041. eCollection 2022.
The addition of Venetoclax (VEN) to Hypomethylating agents (HMAs) significantly improves the probability of complete remission and prolongs survival in patients with Acute Myeloid Leukemia (AML) when compared to HMA alone. However, the mutated clone composition may impact the probability of response and its duration. Here, we describe the molecular profile of a patient with AML rapidly evolved from a previous therapy-related-Chronic MyeloMonocytic Leukemia, who achieved safely complete remission after treatment with the VEN/Azacitidine combination, even in the presence of SARS-COVID-2 infection. The targeted NGS analysis showed that the VEN/AZA combination led to the eradication of the and mutated clone/s primarily associated with AML evolution, and subsequently, the , and mutated clone/s. This case also underlines the importance of the sequential use of targeted NGS for disease monitoring: the deep molecular remission achieved by this patient allowed to safely guide adjustments of drug dosage and treatment intervals in the presence of neutropenia, helping to rule out disease progression.
与单独使用低甲基化药物(HMA)相比,在急性髓系白血病(AML)患者中,将维奈克拉(VEN)添加到低甲基化药物(HMA)中可显著提高完全缓解的概率并延长生存期。然而,突变克隆组成可能会影响缓解概率及其持续时间。在此,我们描述了一名AML患者的分子特征,该患者由先前的治疗相关慢性粒单核细胞白血病迅速演变而来,即使在感染SARS-CoV-2的情况下,接受VEN/阿扎胞苷联合治疗后仍安全地实现了完全缓解。靶向NGS分析表明,VEN/AZA联合治疗导致主要与AML演变相关的 和 突变克隆的根除,随后, 、 和 突变克隆也被根除。该病例还强调了序贯使用靶向NGS进行疾病监测的重要性:该患者实现的深度分子缓解使得在存在中性粒细胞减少的情况下能够安全地指导药物剂量调整和治疗间隔,有助于排除疾病进展。