Marangon Miriam, Visco Carlo, Barbui Anna Maria, Chiappella Annalisa, Fabbri Alberto, Ferrero Simone, Galimberti Sara, Luminari Stefano, Musuraca Gerardo, Re Alessandro, Zilioli Vittorio Ruggero, Ladetto Marco
Department of Hematology, Azienda Sanitaria Universitaria Giuliano Isontina, 34129 Trieste, Italy.
Section of Hematology, Department of Medicine, University of Verona, 37134 Verona, Italy.
Cancers (Basel). 2021 Jan 14;13(2):291. doi: 10.3390/cancers13020291.
MCL is an uncommon lymphoproliferative disorder that has been regarded as incurable since its identification as a distinct entity. Allogeneic transplantation for two decades has represented the only option capable of ensuring prolonged remissions and possibly cure. Despite its efficacy, its application has been limited by feasibility limitations and substantial toxicity, particularly in elderly patients. Nevertheless, the experience accumulated over time has been wide though often scattered among retrospective and small prospective studies. In this review, we aimed at critically revise and discuss available evidence on allogeneic transplantation in MCL, trying to put available evidence into the 2020 perspective, characterized by unprecedented development of novel promising therapeutic agents and regimens.
套细胞淋巴瘤(MCL)是一种罕见的淋巴增殖性疾病,自被确认为一种独特的实体以来,一直被认为是无法治愈的。二十年来,异基因移植一直是唯一能够确保长期缓解并可能治愈的选择。尽管其疗效显著,但其应用受到可行性限制和严重毒性的制约,尤其是在老年患者中。然而,随着时间的推移积累的经验虽然广泛,但往往分散在回顾性研究和小型前瞻性研究中。在本综述中,我们旨在批判性地修订和讨论关于MCL异基因移植的现有证据,试图将现有证据置于2020年的背景下,这一时期以新型有前景的治疗药物和方案的前所未有的发展为特征。