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Mantle Cell Lymphoma Current and Emerging Treatment Strategies and Unanswered Questions

机译:地幔细胞淋巴瘤当前和新兴的治疗策略和未答复的问题

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摘要

Mantle cell lymphoma (MCL) is biologically and clinically heterogeneous with no clear standard of care. Overexpression of cyclin D1 is a hallmark of MCL. Evolving characterization of other molecular drivers explain a variety of disease phenotypes. These molecular profiles challenge risk stratification techniques. TP53-deleted disease is associated with adverse outcomes. Frontline treatment programs include intensive chemoimmunotherapy and autologous stem cell transplantation. Minimal residual disease may change management of MCL and guide therapy. As commonly dysregulated pathways become enumerated, novel biologically targeted agents and their combinations have been developed that will increasingly replace older, more toxic, and less efficacious regimens.
机译:Mantle细胞淋巴瘤(MCL)在生物学和临床上异质,没有明确的护理标准。 细胞周期蛋白D1的过度表达是MCL的标志。 不断发展的其他分子司机的表征解释了各种疾病表型。 这些分子曲线挑战风险分层技术。 TP53缺失的疾病与不利结果有关。 前线治疗计划包括密集的化疗和自体干细胞移植。 最小的残留疾病可能会改变MCL和指导治疗的管理。 随着常见的失调途径变列,已经开发了新的生物靶向剂及其组合,这将越来越多地替代较旧的,更具毒性和更不效益的方案。

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