Department of Radiation Oncology, Ege University Medical School, Izmir, Turkey.
Int J Radiat Oncol Biol Phys. 2012 Jan 1;82(1):315-20. doi: 10.1016/j.ijrobp.2010.09.046. Epub 2010 Nov 13.
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.
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.
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).
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.
唾液腺黏膜相关淋巴组织(MALT)淋巴瘤的腺体受累罕见。本回顾性研究旨在评估唾液腺 MALT 淋巴瘤的临床特征、治疗结果和预后因素。
来自 10 个国家的 13 个罕见癌症网络成员中心参与了此项研究,提供了 63 例患者的数据。中位年龄为 58 岁;47 例为女性,16 例为男性。49 例累及腮腺,15 例累及颌下腺,3 例累及小唾液腺。9 例患者有多个腺体受累。分期如下:IE 期 34 例,IIE 期 12 例,III 期 2 例,IV 期 15 例。
9 例患者仅接受手术(S)治疗,8 例患者仅接受放疗(RT)治疗,4 例患者仅接受化疗(CT)治疗。41 例患者接受了联合治疗(23 例接受 S+RT,8 例接受 S+CT,4 例接受 RT+CT,6 例接受所有三种治疗)。1 例患者未接受积极治疗。初始治疗后,57 例患者肿瘤无残留,5 例患者有肿瘤残留。23 例患者出现肿瘤进展(局部 1 例,其他唾液腺 10 例,淋巴结 11 例,其他部位 6 例)。5 例患者死于疾病进展,5 例患者死于其他原因。5 年无病生存率、疾病特异性生存率和总生存率分别为 54.4%、93.2%和 81.7%。影响无病生存率的因素为 RT 的使用、分期和残留肿瘤(p<0.01)。影响疾病特异性生存率的因素为分期、复发和残留肿瘤(p<0.01)。
据我们所知,这是迄今为止发表的最大系列唾液腺 MALT 淋巴瘤报告。该疾病最初或随后可累及所有唾液腺,发生率为 30%。5 年内复发率可达 35%;然而,生存并未受到影响。放疗是唯一能提高无病生存率的治疗方法。