Sperotto Alessandra, Stanghellini Maria Teresa Lupo, Peccatori Jacopo, De Marchi Roberta, Piemontese Simona, Ciotti Giulia, Basso Marco, Pierdomenico Elisabetta, Fiore Paolo, Ciceri Fabio, Gottardi Michele
Onco Hematology, Department of Oncology, Veneto Institute of Oncology, Istituto Oncologico Veneto-Istituto di Ricerca e Cura a Carattere Scientifico (IOV-IRCCS), Castelfranco Veneto, Italy.
Hematology and Hematopoietic Stem Cell Transplantation Unit, Istituto di Ricerca e Cura a Carattere Scientifico (IRCCS) San Raffaele Scientific Institute, Milano, Italy.
Front Oncol. 2024 Jan 25;13:1291457. doi: 10.3389/fonc.2023.1291457. eCollection 2023.
Therapy-related myeloid neoplasms (t-MNs), which develop after cytotoxic, radiation, or immunosuppressive therapy for an unrelated disease, account for 7%-8% of acute myeloid leukemia (AML). Worse outcomes and consequently shortened survival are associated with t-MNs as compared with AML. Therapy-related MNs are being reported with increasing frequency in successfully treated acute promyelocytic leukemia (APL), in particular, before the introduction of all- retinoic acid (ATRA) plus arsenic trioxide (ATO). Considering the high curability of APL, t-MNs represent one of the prognosis-limiting factors in this setting of leukemia. We report our experience with a patient who developed t-AML 15 years after treatment for APL. Treatment included three cycles of chemotherapy with CPX-351 (Vyxeos, Jazz Pharmaceuticals) followed, as in remission, by an allogeneic hematopoietic stem cell transplant. A review of available literature was also included.
治疗相关髓系肿瘤(t-MNs)是在针对无关疾病进行细胞毒性、放射或免疫抑制治疗后发生的,占急性髓系白血病(AML)的7%-8%。与AML相比,t-MNs的预后更差,生存期因此缩短。在成功治疗的急性早幼粒细胞白血病(APL)中,尤其是在引入全反式维甲酸(ATRA)加三氧化二砷(ATO)之前,治疗相关髓系肿瘤的报告频率越来越高。鉴于APL的高治愈率,t-MNs是这种白血病预后的限制因素之一。我们报告了一名患者在接受APL治疗15年后发生t-AML的经历。治疗包括三个周期的CPX-351(Vyxeos,Jazz制药公司)化疗,缓解后进行异基因造血干细胞移植。还对现有文献进行了综述。