Department of Radiation Oncology, Duke University Medical Center, Durham, North Carolina.
Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, North Carolina.
Int J Radiat Oncol Biol Phys. 2019 Sep 1;105(1):96-101. doi: 10.1016/j.ijrobp.2019.02.055. Epub 2019 Mar 8.
To evaluate the feasibility of reducing the dose of consolidation radiation therapy (RT) in diffuse large B-cell lymphoma.
This phase 2 study enrolled patients with diffuse large B-cell lymphoma, not otherwise specified and primary mediastinal (thymic) large B-cell lymphoma in complete response on positron emission tomography-computed tomography imaging after ≥4 cycles of a rituximab/anthracycline-containing combination chemotherapy regimen. Consolidation RT used a dose of 19.5 to 20 Gy. The primary endpoint was 5-year freedom from local recurrence.
Sixty-two patients were enrolled between 2010 and 2016. Stage distribution was as follows: I to II (n = 49, 79%) and III to IV (n = 13, 21%). Bulky disease (defined as ≥7.5 cm or ≥10 cm) was present in 23 (40%) and 16 (28%) patients, respectively. Chemotherapy was R-CHOP (then list the drugs) in 58 (94%) and R-EPOCH (then list the drugs) in 4 (6%) with a median of 6 cycles. With a median follow-up of 51 months, 7 patients developed disease progression (6 outside the RT field, 1 within the RT field). Freedom from local recurrence at 5 years was 98% (90% lower confidence bound, 88%). Progression-free and overall survival at 5 years were 83% and 90%, respectively.
With more effective systemic therapy (e.g., addition of rituximab) and more refined chemotherapy response assessment (e.g., positron emission tomography-computed tomography), the dose of RT in combined modality treatment programs may potentially be reduced to 20 Gy. This achieves excellent local control with the potential to decrease acute and long-term side effects.
评估降低弥漫性大 B 细胞淋巴瘤巩固放疗剂量的可行性。
本 2 期研究纳入了在完成利妥昔单抗/蒽环类药物联合化疗≥4 周期后,正电子发射断层扫描/计算机断层扫描成像达到完全缓解的非特指弥漫性大 B 细胞淋巴瘤和原发性纵隔(胸腺)大 B 细胞淋巴瘤患者。巩固放疗剂量为 19.5 至 20 Gy。主要终点为 5 年局部无复发生存率。
2010 年至 2016 年期间共纳入 62 例患者。分期分布如下:I 期至 II 期(n=49,79%)和 III 期至 IV 期(n=13,21%)。23 例(40%)和 16 例(28%)患者存在大肿块疾病(定义为≥7.5 cm 或≥10 cm)。58 例(94%)患者接受 R-CHOP(列出药物)化疗,4 例(6%)接受 R-EPOCH(列出药物)化疗,中位化疗周期数为 6 个。中位随访 51 个月时,7 例患者发生疾病进展(6 例在放疗野外,1 例在放疗野内)。5 年局部无复发生存率为 98%(90%置信区间下限,88%)。5 年无进展生存率和总生存率分别为 83%和 90%。
随着更有效的全身治疗(例如,加入利妥昔单抗)和更精细的化疗反应评估(例如,正电子发射断层扫描/计算机断层扫描),联合治疗方案中的放疗剂量可能降低至 20 Gy。这可以实现优异的局部控制,并有降低急性和长期副作用的潜力。