在现实世界的临床实践中,高级别非霍奇金淋巴瘤患者的放疗剂量递减

IF 1.8 Q3 ONCOLOGY Radiation Oncology Journal Pub Date : 2023-09-25 DOI:10.3857/roj.2023.00339
Budhi Singh Yadav, Treshita Dey
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引用次数: 0

摘要

非霍奇金淋巴瘤(NHL)的标准治疗包括联合治疗、放疗(RT)和利妥昔单抗化疗,利妥昔单抗显著提高了无病生存期(DFS)和总生存期(OS)。然而,这些患者的辐射剂量使用并不均匀。在这项回顾性研究中,我们比较了侵袭性非霍奇金淋巴瘤患者的低辐射剂量和高辐射剂量。材料与方法纳入2007 - 2017年所有高级别NHL或弥漫性大b细胞淋巴瘤和非中枢神经系统NHL的治疗记录。我们比较了接受¤30 Gy放疗与接受>30 Gy放疗的患者的有效率、OS和DFS。通过单因素和多因素分析确定影响预后的因素,即年龄、性别、分期、国际预后指数(IPI)、添加利妥昔单抗和放疗剂量。结果分析了184例合并放疗或单独放疗的NHL患者的完整随访资料。中位随访66.8个月时,高剂量组5年OS为72.8%,低剂量组为69.9% (p = 0.772); 5年DFS为64.7%,低剂量组为64.1% (p = 0.871)。低剂量治疗的早期疾病患者和>30 Gy治疗的晚期疾病患者的OS和DFS更好,但无统计学意义。添加利妥昔单抗与更好的OS和DFS相关,与放射剂量无关。IPI评分高和未使用美罗华是导致OS和DFS显著恶化的唯一因素。两组的急性放射毒性比较(p = 0.82)。在晚期毒性中,没有患者发生第二次恶性肿瘤,5%的患者死于心血管并发症(p = 0.595),尽管只有2例患者(1.1%)接受了胸部放射治疗。结论两组有效率、急性毒性、DFS和OS相当。这项研究表明,在不影响DFS和OS的情况下,在高级别NHL中减少放疗剂量是可能的。关键词:非霍奇金淋巴瘤,放疗,晚期效应,放疗剂量递减
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Radiotherapy dose de-escalation in patients with high grade non-Hodgkin lymphoma in a real-world clinical practice
Purpose The standard treatment of non-Hodgkin lymphoma (NHL) comprises combined modality treatment, radiotherapy (RT), and chemotherapy with rituximab which has significantly improved both disease-free survival (DFS) and overall survival (OS). However, there is no uniformity in radiation dose usage in these patients. In this retrospective study, we compared lower radiation dose with higher in patients with aggressive NHL. Materials and Methods From 2007 to 2017, treatment records of all high-grade NHL or diffuse large B-cell lymphoma and non-central nervous system NHL were included. We compared response rates, OS and DFS of patients who received ≤30 Gy RT to those with >30 Gy. Univariate and multivariate analyses were done to determine factors affecting prognosis, i.e., age, sex, stage, International Prognostic Index (IPI), adding rituximab, and radiation dose. Results A total of 184 NHL patients treated with combined modality or radiation alone having complete follow-up details were analyzed. At median follow-up of 66.8 months, 5-year OS was 72.8% in high-dose group versus 69.9% in low-dose group (p = 0.772) and 5-year DFS 64.7% versus 64.1% (p = 0.871). Patients having early-stage disease receiving low dose and those with advanced disease treated with >30 Gy had better OS and DFS though not statistically significant. Adding rituximab was associated with significantly better OS and DFS irrespective of radiation dose delivered. High IPI score and omitting rituximab were the only factors that significantly worsened both OS and DFS. Acute radiation toxicities were comparable in both groups (p = 0.82). Among late toxicities, no patient developed a second malignancy and 5% died due to cardiovascular complications (p = 0.595) though only two patients (1.1%) had received thoracic radiation. Conclusion The two groups had comparable response rates, acute toxicities, DFS and OS. This study suggests that RT dose reduction may be possible in high-grade NHL without compromising the DFS and OS. Keywords: Non-Hodgkin lymphoma, Radiotherapy, Late effects, Radiation dose de-escalation
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