Wijetunga N Ari, Yahalom Joachim, Imber Brandon S
Department of Radiation Oncology, University of North Carolina, Chapel Hill, NC, United States.
Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Front Oncol. 2025 Mar 21;14:1478078. doi: 10.3389/fonc.2024.1478078. eCollection 2024.
It is well established that hematologic malignancies are often considerably radiosensitive, which enables usage of far lower doses of therapeutic radiotherapy. This review summarizes the currently known genomic landscape of hematologic malignancies, particularly as it relates to radiosensitivity and the field of radiation oncology. By tracing the historical development of the modern understanding of radiosensitivity, we focus on the discovery and implications of pivotal mutated genes in hematologic malignancies such as and other genes critical to DNA repair pathways. These genetic insights have contributed significantly to the advancement of personalized medicine, aiming to enhance treatment precision and outcomes, and there is an opportunity to extend these insights to personalized radiotherapy. We explore the transition from early discoveries to the current efforts in integrating comprehensive genomic data into clinical practice. Specific examples from Hodgkin lymphoma, non-Hodgkin lymphoma, and plasma cell neoplasms illustrate how genetic mutations could influence radiosensitivity and impact subsequent radiotherapeutic response. Despite the advancements, challenges remain in translating these genetic insights into routine clinical practice, particularly due to the heterogeneity of alterations and the complex interactions within cancer signaling pathways. We emphasize the potential of radiogenomics to address these challenges by identifying genetic markers that predict radiotherapy response and toxicity, thereby refining treatment strategies. The need for robust decision support systems, standardized protocols, and ongoing education for healthcare providers is critical to the successful integration of genomic data into radiation therapy. As research continues to validate genetic markers and explore novel therapeutic combinations, the promise of personalized radiotherapy becomes increasingly attainable, offering the potential to significantly improve outcomes for patients with hematologic malignancies.
血液系统恶性肿瘤通常对放疗相当敏感,这使得在治疗性放疗中可以使用低得多的剂量,这一点已得到充分证实。本综述总结了目前已知的血液系统恶性肿瘤的基因组格局,特别是与放射敏感性和放射肿瘤学领域相关的方面。通过追溯现代对放射敏感性理解的历史发展,我们关注血液系统恶性肿瘤中关键突变基因的发现及其意义,如以及对DNA修复途径至关重要的其他基因。这些遗传学见解对精准医学的发展做出了重大贡献,旨在提高治疗的精准度和疗效,并且有机会将这些见解扩展到个性化放疗。我们探讨了从早期发现到目前将综合基因组数据整合到临床实践中的努力的转变。霍奇金淋巴瘤、非霍奇金淋巴瘤和浆细胞肿瘤的具体例子说明了基因突变如何影响放射敏感性并影响随后的放射治疗反应。尽管取得了进展,但将这些遗传学见解转化为常规临床实践仍面临挑战,特别是由于改变的异质性和癌症信号通路内的复杂相互作用。我们强调放射基因组学通过识别预测放疗反应和毒性的遗传标记来应对这些挑战的潜力,从而优化治疗策略。强大的决策支持系统、标准化方案以及对医疗保健提供者的持续教育对于将基因组数据成功整合到放射治疗中至关重要。随着研究继续验证遗传标记并探索新的治疗组合,个性化放疗的前景越来越可期,有望显著改善血液系统恶性肿瘤患者的治疗效果。