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肺黏膜相关边缘区 B 细胞淋巴瘤患者的治疗结果。

Treatment outcomes in patients with extranodal marginal zone B-cell lymphoma of the lung.

机构信息

Division of Pulmonology and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

J Thorac Cardiovasc Surg. 2017 Jul;154(1):342-349. doi: 10.1016/j.jtcvs.2017.03.043. Epub 2017 Mar 21.

Abstract

OBJECTIVES

To evaluate clinical presentations, treatment modalities, and outcomes of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma by stage strata.

METHODS

We retrospectively reviewed 51 patients diagnosed with pulmonary MALT lymphoma between January 2003 and December 2015. To compare treatment modalities and outcomes, we stratified the patients into low-stage (IE/IIE) and high-stage (IIIE/IVE) groups using modified Ann Arbor staging. Progression-free survival was estimated using Kaplan-Meier curves, and differences were compared using the log-rank test. A hazard ratio of progression by stage strata, adjusted for other clinical variables, was determined using a Cox adjusted proportional hazards model.

RESULTS

The majority of patients had stage IE disease (76.5%; 39 of 51). With advancing stage, patients were more likely to have respiratory and B symptoms and higher International Prognostic Index scores. The most common treatment modality was surgical resection in low-stage patients (33 of 43) and chemotherapy in high-stage patients (7 of 8). At a median follow-up of 40.7 months, progression-free survival was longer for low-stage patients (median, 40.7 months vs 24.9 months; P < .001), and high-stage patients were 9.2 times more likely to progress (hazard ratio, 9.24; 95% confidence interval, 1.93-44.36). Among 30 patients with surgically resected stage IE disease, 8 with central lesions were treated via lobectomy and 22 with peripheral lesions were treated via lobectomy (n = 8) or limited resection (n = 14). One of these patients, with a central lesion, experienced disease recurrence.

CONCLUSIONS

Our findings suggest that the clinical course of low-stage pulmonary MALT lymphoma, for which the mainstay of treatment is surgical resection, might be indolent.

摘要

目的

通过分期分层评估肺黏膜相关淋巴组织(MALT)淋巴瘤的临床表现、治疗方式和结局。

方法

我们回顾性分析了 2003 年 1 月至 2015 年 12 月期间诊断为肺 MALT 淋巴瘤的 51 例患者。为了比较治疗方式和结局,我们使用改良的 Ann Arbor 分期将患者分为低分期(IE/IIE)和高分期(IIIE/IVE)组。使用 Kaplan-Meier 曲线估计无进展生存期,并使用对数秩检验比较差异。使用 Cox 调整比例风险模型确定按分期分层的进展风险比,同时调整其他临床变量。

结果

大多数患者患有 IE 期疾病(76.5%,51 例中的 39 例)。随着分期的进展,患者更有可能出现呼吸和 B 症状以及更高的国际预后指数评分。低分期患者最常见的治疗方式是手术切除(43 例中的 33 例),高分期患者是化疗(8 例中的 7 例)。在中位随访 40.7 个月时,低分期患者的无进展生存期更长(中位时间,40.7 个月 vs 24.9 个月;P<0.001),高分期患者进展的可能性高 9.2 倍(风险比,9.24;95%置信区间,1.93-44.36)。在 30 例接受手术切除的 IE 期疾病患者中,8 例中央病变患者接受肺叶切除术,22 例周围病变患者接受肺叶切除术(n=8)或有限切除术(n=14)。其中 1 例中央病变患者出现疾病复发。

结论

我们的研究结果表明,以手术切除为主要治疗方法的低分期肺 MALT 淋巴瘤的临床病程可能是惰性的。

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