Radiation Therapy Program, BC Cancer Agency, Vancouver and Victoria, BC.
Clin Breast Cancer. 2012 Dec;12(6):412-9. doi: 10.1016/j.clbc.2012.07.006. Epub 2012 Sep 25.
To evaluate treatment and outcomes in a population-based cohort of patients diagnosed with primary breast lymphoma.
Prognostic factors, management, and outcomes (local control, lymphoma-specific survival, and overall survival) were analyzed for all patients diagnosed with limited-stage, primary breast non-Hodgkin lymphoma (n = 50) diagnosed in British Columbia between 1981 and 2009.
The median follow-up was 3.5 years; 64% presented with a breast mass. Histologic subtypes were indolent (n = 16 [32%]) or aggressive (n = 34 [68%]). Of those with indolent lymphoma, 81% had stage I, and 19% had stage II disease; 13% received no initial treatment; 75% received radiotherapy (RT) alone. One (6%) patient received surgical resection alone, and 1 (6%) patient received surgical resection in addition to RT. Of those with aggressive lymphoma, 62% had stage I and 38% had stage II disease; 3% received no initial treatment; 6%, RT alone; 38%, chemotherapy only; 41%, chemotherapy and RT; 9%, surgical resection alone; and 3%, surgical resection in addition to chemotherapy and RT. In patients with indolent and aggressive disease, 5-year local control estimates were 92% and 96%, lymphoma-specific survivals were 91% and 71%, and overall survivals were 75% and 54%, respectively. On univariate analysis, stage (I vs. II) (P = .006) and RT use (P = .032) were statistically significant predictors of improved overall survival in patients with indolent breast lymphoma. Combined chemoradiation was associated with a trend for improved overall survival (P = .061) in patients with aggressive disease. There were 4 cases of central nervous system relapse, all occurred in subjects with aggressive primary breast lymphoma.
Patients with indolent breast lymphoma were most frequently treated with RT alone and achieved high rates of local control and survival. Patients with aggressive histology most often treated with chemotherapy, alone or combined with RT, had excellent local control but lower survival compared with indolent disease. Improved systemic therapies are needed to improve outcomes for patients with aggressive breast lymphoma.
评估在不列颠哥伦比亚省诊断为原发性乳腺淋巴瘤的人群中进行治疗和结局。
分析了 1981 年至 2009 年间在不列颠哥伦比亚省诊断为局限性原发性乳腺非霍奇金淋巴瘤(n = 50)的所有患者的预后因素、治疗方法和结局(局部控制、淋巴瘤特异性生存和总生存)。
中位随访时间为 3.5 年;64%的患者表现为乳房肿块。组织学亚型为惰性(n = 16 [32%])或侵袭性(n = 34 [68%])。惰性淋巴瘤患者中,81%为 I 期,19%为 II 期;13%未接受初始治疗;75%单独接受放疗(RT)。1 名(6%)患者仅接受手术切除,1 名(6%)患者在接受 RT 后接受手术切除。侵袭性淋巴瘤患者中,62%为 I 期,38%为 II 期;3%未接受初始治疗;6%单独接受 RT;6%仅接受化疗;38%接受化疗和 RT;9%仅接受手术切除;3%在接受化疗和 RT 后接受手术切除。在惰性和侵袭性疾病患者中,5 年局部控制估计分别为 92%和 96%,淋巴瘤特异性生存率分别为 91%和 71%,总生存率分别为 75%和 54%。单因素分析显示,分期(I 期与 II 期)(P =.006)和 RT 应用(P =.032)是影响惰性乳腺淋巴瘤患者总生存的统计学显著预测因素。在侵袭性疾病患者中,联合化疗和放疗与总生存的改善趋势相关(P =.061)。有 4 例中枢神经系统复发,均发生在侵袭性原发性乳腺淋巴瘤患者中。
大多数患有惰性乳腺淋巴瘤的患者单独接受 RT 治疗,局部控制和生存率较高。大多数患有侵袭性组织学的患者接受化疗单独或联合 RT 治疗,局部控制良好,但与惰性疾病相比,生存率较低。需要改进全身治疗,以改善侵袭性乳腺淋巴瘤患者的结局。