鼻窦非霍奇金恶性淋巴瘤——53例患者按REAL分类的治疗结果

Non-Hodgkin's malignant lymphoma of the sinonasal tract--treatment outcome for 53 patients according to REAL classification.

作者信息

Hatta C, Ogasawara H, Okita J, Kubota A, Ishida M, Sakagami M

机构信息

Department of Otolaryngology, Hyogo College of Medicine, 1-1 Mukogawa, Nishinomiya, 663-8501, Hyogo, Japan.

出版信息

Auris Nasus Larynx. 2001 Jan;28(1):55-60. doi: 10.1016/s0385-8146(00)00094-8.

Abstract

OBJECTIVE

Although the Working Formulation is commonly used to classify NHL in Japan, it has been recognized as imperfect for primary extranodal lymphoma, especially for patients with sinonasal disease because of their histological characteristics. The present study investigated the clinical characteristics and the prognosis of sinonasal lymphomas according to REAL classification.

METHODS

Fifty-three patients with non-Hodgkin's malignant lymphoma (NHL) of the sinonasal tract were treated between 1981 and 1997. The age at clinical presentation was from 10 to 84 years (mean, 52.4 years). According to the Ann Arbor system, there were 30 patients with Stage IE, 13 with Stage IIE, 4 with Stage IIIE, and 6 with Stage IVE lymphomas. Twenty-two patients (41.5%) had B symptoms. The primary sites were the nasal cavity (67.8%), maxillary sinus (20.8%), ethmoidal sinus (9.4%), and frontal sinus (1.9%). The survival data was calculated by Kaplan-Meier method. Statistical analysis was performed with a generalized Wilcoxon method.

RESULTS

All of the lymphomas showed a diffuse growth pattern. Based on the origin of the tumor cells, the authors classified NHL of the sinonasal tract into five groups with the REAL classification of Japan: diffuse large B-cell lymphoma (22.6%), peripheral T-cell lymphomas (15.1%), angiocentric lymphoma (35.9%), other lymphomas and unclassified types. Of 53 patients, 39 (73.6%) received chemotherapy and radiotherapy, eight patients received chemotherapy alone, and four patients received radiotherapy alone. The cumulative 5-year survival rates were 28.5% for all of the types, 55.0% for diffuse large B-cell lymphoma, 33.3% for peripheral T-cell lymphoma, and 19.7% for angiocentric lymphoma. Results suggest that conventional combined treatment (CHOP chemotherapy+radiotherapy) is ineffective for NHL of the sinonasal tract, and especially so for NHL in the nasal cavity, NHL with tumor cells with positive T-cell markers, NHL further than Stage IIE and NHL with B symptoms.

CONCLUSION

(1) In light of this ineffectiveness, new therapies must be developed to improve patient outcome instead of the conventional combined treatment; (2) REAL classification is clear and useful for sinonasal lymphomas in Japan.

摘要

目的

尽管工作分类法在日本常用于非霍奇金淋巴瘤(NHL)的分类,但由于其组织学特征,该分类法已被认为对于原发性结外淋巴瘤并不完善,尤其是对于鼻窦疾病患者。本研究根据修订的欧美淋巴瘤分类(REAL分类)调查了鼻窦淋巴瘤的临床特征和预后。

方法

1981年至1997年间,对53例鼻窦非霍奇金恶性淋巴瘤(NHL)患者进行了治疗。临床表现时的年龄为10至84岁(平均52.4岁)。根据Ann Arbor分期系统,有30例IE期淋巴瘤患者,13例IIE期患者,4例IIIE期患者和6例IVE期淋巴瘤患者。22例患者(41.5%)有B症状。原发部位为鼻腔(67.8%)、上颌窦(20.8%)、筛窦(9.4%)和额窦(1.9%)。生存数据采用Kaplan-Meier法计算。采用广义Wilcoxon法进行统计分析。

结果

所有淋巴瘤均表现为弥漫性生长模式。根据肿瘤细胞的起源,作者将日本REAL分类法中的鼻窦NHL分为五组:弥漫性大B细胞淋巴瘤(22.6%)、外周T细胞淋巴瘤(15.1%)、血管中心性淋巴瘤(35.9%)、其他淋巴瘤和未分类类型。53例患者中,39例(73.6%)接受了化疗和放疗,8例患者仅接受化疗,4例患者仅接受放疗。所有类型的5年累积生存率为28.5%,弥漫性大B细胞淋巴瘤为55.0%,外周T细胞淋巴瘤为33.3%,血管中心性淋巴瘤为19.7%。结果表明,传统的联合治疗(CHOP化疗+放疗)对鼻窦NHL无效,尤其是对鼻腔NHL、肿瘤细胞T细胞标志物阳性的NHL、IIE期以上的NHL和有B症状的NHL无效。

结论

(1)鉴于这种无效性,必须开发新的疗法以改善患者预后,而不是采用传统的联合治疗;(2)REAL分类法对日本的鼻窦淋巴瘤清晰且有用。

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