首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Primary mucosa-associated lymphoid tissue lymphoma of the salivary glands: A multicenter rare cancer network study
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Primary mucosa-associated lymphoid tissue lymphoma of the salivary glands: A multicenter rare cancer network study

机译:涎腺原发性黏膜相关淋巴组织淋巴瘤:多中心罕见癌症网络研究

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Purpose: Involvement of salivary glands with mucosa-associated lymphoid tissue (MALT) lymphoma is rare. This retrospective study was performed to assess the clinical profile, treatment outcome, and prognostic factors of MALT lymphoma of the salivary glands. Methods and Materials: Thirteen member centers of the Rare Cancer Network from 10 countries participated, providing data on 63 patients. The median age was 58 years; 47 patients were female and 16 were male. The parotid glands were involved in 49 cases, submandibular in 15, and minor glands in 3. Multiple glands were involved in 9 patients. Staging was as follows: IE in 34, IIE in 12, IIIE in 2, and IV in 15 patients. Results: Surgery (S) alone was performed in 9, radiotherapy (RT) alone in 8, and chemotherapy (CT) alone in 4 patients. Forty-one patients received combined modality treatment (S + RT in 23, S + CT in 8, RT + CT in 4, and all three modalities in 6 patients). No active treatment was given in one case. After initial treatment there was no tumor in 57 patients and residual tumor in 5. Tumor progression was observed in 23 (36.5%) (local in 1, other salivary glands in 10, lymph nodes in 11, and elsewhere in 6). Five patients died of disease progression and the other 5 of other causes. The 5-year disease-free survival, disease-specific survival, and overall survival were 54.4%, 93.2%, and 81.7%, respectively. Factors influencing disease-free survival were use of RT, stage, and residual tumor (p < 0.01). Factors influencing disease-specific survival were stage, recurrence, and residual tumor (p < 0.01). Conclusions: To our knowledge, this report represents the largest series of MALT lymphomas of the salivary glands published to date. This disease may involve all salivary glands either initially or subsequently in 30% of patients. Recurrences may occur in up to 35% of patients at 5 years; however, survival is not affected. Radiotherapy is the only treatment modality that improves disease-free survival.
机译:目的:唾液腺受粘膜相关淋巴样组织(MALT)淋巴瘤的侵害很少。进行这项回顾性研究以评估唾液腺MALT淋巴瘤的临床概况,治疗结果和预后因素。方法和材料:来自10个国家的13个罕见癌网络成员中心参加了此次会议,提供了63位患者的数据。中位年龄是58岁。女性47例,男性16例。腮腺49例,颌下15例,小腺3例。多发腺9例。分期如下:IE为34,IEE为12,IIIE为2,IV为15例。结果:9例仅接受外科手术(S),8例仅接受放射治疗(RT),4例仅接受化学疗法(CT)。 41例患者接受了联合方式治疗(23例接受S + RT,8例接受S + CT,4例接受RT + CT,6例均接受三种方式)。 1例未给予积极治疗。初始治疗后,57例患者中没有肿瘤,5例中残留肿瘤。23例(36.5%)观察到肿瘤进展(局部位于1个,其他唾液腺位于10个,淋巴结在11个,其他在6个)。五例患者死于疾病进展,另外五例死于其他原因。 5年无病生存期,疾病特异性生存期和总生存期分别为54.4%,93.2%和81.7%。影响无病生存的因素是放疗,分期和残余肿瘤的使用(p <0.01)。影响疾病特异性生存的因素是分期,复发和残留肿瘤(p <0.01)。结论:据我们所知,本报告代表了迄今为止发表的最大的唾液腺MALT淋巴瘤系列。该疾病可能在30%的患者中最初或之后累及所有唾液腺。 5年时高达35%的患者可能会复发。但是,生存期不受影响。放射疗法是提高无病生存率的唯一治疗方法。

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