Baylor College of Medicine, Houston, TX.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2019 Jan;19(1):e51-e61. doi: 10.1016/j.clml.2018.09.002. Epub 2018 Sep 10.
We report successful treatment of mesenteric diffuse large B-cell lymphoma (DLBCL) using localized involved site radiation therapy (ISRT), intensity modulated radiation therapy (IMRT), and daily computed tomography (CT)-image guidance.
Patients with mesenteric DLBCL treated with RT between 2011 and 2017 were reviewed. Clinical and treatment characteristics were analyzed for an association with local control, progression-free survival (PFS), and overall survival.
Twenty-three patients were eligible. At diagnosis, the median age was 52 years (range, 38-76 years), and 57% (n = 13) had stage I/II DLBCL. All patients received frontline chemotherapy (ChT) (R-CHOP [rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone], n = 19; dose-adjusted R-EPOCH [rituximab, etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin], n = 4) with median 6 cycles. Prior to RT, salvage ChT for refractory DLBCL was given to 43% (n = 10) and autologous stem cell transplantation was administered in 13% (n = 3). At the time of RT, positron emission tomography-CT revealed 5-point scale of 1 to 3 (48%; n = 11), 4 (9%; n = 2), and 5 (44%; n = 10). All patients received IMRT, daily CT imaging, and ISRT. The median RT dose was 40 Gy (range, 16.2-49.4 Gy). Relapse or progression occurred in 22% (n = 5). At a median follow-up of 37 months, the 3-year local control, PFS, and overall survival rates were 80%, 75%, and 96%, respectively. Among patients treated with RT after complete metabolic response to frontline ChT (n = 8), the 3-year PFS was 100%, compared with 61% for patients with a history of chemorefractory DLBCL (n = 15; P = .055). Four of the 5 relapses occurred in patients with 5-point scale of 5 prior to RT (P = .127).
Mesenteric involvement of DLBCL can be successfully targeted with localized ISRT fields using IMRT and daily CT-image guidance.
我们报告了使用局部受累部位放射治疗(ISRT)、调强放射治疗(IMRT)和每日计算机断层扫描(CT)图像引导成功治疗肠系膜弥漫性大 B 细胞淋巴瘤(DLBCL)的情况。
回顾了 2011 年至 2017 年间接受 RT 治疗的肠系膜 DLBCL 患者。分析了临床和治疗特征与局部控制、无进展生存期(PFS)和总生存期的关系。
23 名患者符合条件。在诊断时,中位年龄为 52 岁(范围,38-76 岁),57%(n=13)为 I/II 期 DLBCL。所有患者均接受一线化疗(ChT)(R-CHOP[利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松],n=19;剂量调整的 EPOCH[利妥昔单抗、依托泊苷、泼尼松、长春新碱、环磷酰胺和多柔比星],n=4),中位周期数为 6 个。在 RT 前,43%(n=10)的患者接受了难治性 DLBCL 的挽救性 ChT,13%(n=3)的患者接受了自体干细胞移植。在 RT 时,正电子发射断层扫描-CT 显示 5 分制为 1-3(48%;n=11)、4(9%;n=2)和 5(44%;n=10)。所有患者均接受 IMRT、每日 CT 成像和 ISRT。中位 RT 剂量为 40Gy(范围,16.2-49.4Gy)。22%(n=5)出现复发或进展。中位随访 37 个月后,3 年局部控制、PFS 和总生存率分别为 80%、75%和 96%。在接受一线 ChT 完全代谢反应后接受 RT 治疗的 8 名患者中,3 年 PFS 为 100%,而既往有化疗难治性 DLBCL 病史的 15 名患者为 61%(P=0.055)。5 次复发中有 4 次发生在 RT 前 5 分制为 5 的患者中(P=0.127)。
使用 IMRT 和每日 CT 图像引导,可成功地用局部 ISRT 野靶向治疗肠系膜 DLBCL。