Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Blood. 2011 Feb 10;117(6):1958-65. doi: 10.1182/blood-2010-06-288480. Epub 2010 Dec 9.
The aim of this retrospective cohort study was to analyze the impact of surgery on the outcomes and qualities of life (QOL) in patients with intestinal diffuse large B-cell lymphoma (DLBCL). We assessed 345 patients with either localized or disseminated intestinal DLBCL and compared them according to treatment: surgical resection followed by chemotherapy versus chemotherapy alone. In patients with localized disease (Lugano stage I/II), surgery plus chemotherapy yielded a lower relapse rate (15.3%) than did chemotherapy alone (36.8%, P < .001). The 3-year overall survival rate was 91% in the surgery plus chemotherapy group and 62% in the chemotherapy-alone group (P < .001). The predominant pattern in the chemotherapy group was local relapse (27.6%). When rituximab was used with cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP), there was no improvement of the outcomes in patients treated with primary surgical resection. The QOL of patients who underwent surgery and chemotherapy was lower than chemotherapy alone, but its difference was acceptable. Multivariate analysis showed that surgical resection plus chemotherapy was an independent prognostic factor for overall survival. Surgical resection followed by chemotherapy might be an effective treatment strategy with acceptable QOL deterioration for localized intestinal DLBCL. This study was registered at www.clinicaltrials.gov as #NCT01043302.
本回顾性队列研究旨在分析手术对肠道弥漫性大 B 细胞淋巴瘤(DLBCL)患者结局和生活质量(QOL)的影响。我们评估了 345 例局限或播散性肠道 DLBCL 患者,并根据治疗方式进行了比较:手术切除联合化疗与单纯化疗。在局限疾病(Lugano 分期 I/II)患者中,手术加化疗的复发率(15.3%)低于单纯化疗(36.8%,P <.001)。手术加化疗组的 3 年总生存率为 91%,单纯化疗组为 62%(P <.001)。化疗组的主要复发模式为局部复发(27.6%)。当环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)联合利妥昔单抗使用时,原发手术切除患者的结局并未改善。接受手术和化疗的患者的 QOL 低于单纯化疗,但差异是可以接受的。多变量分析表明,手术切除加化疗是总生存的独立预后因素。对于局限的肠道 DLBCL,手术切除联合化疗可能是一种有效的治疗策略,其 QOL 恶化是可以接受的。本研究在 www.clinicaltrials.gov 注册,编号为 #NCT01043302。