Lee Victor Ho-Fun, Tsang Raymond King-Yin, Lo Anthony Wing Ip, Chan Sum-Yin, Chung Joseph Chun-Kit, Tong Chi-Chung, Leung To-Wai, Kwong Dora Lai-Wan
Department of Clinical Oncology, School of Clinical Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Department of Clinical Oncology, Queen Mary Hospital, Hong Kong, China.
Cancers (Basel). 2022 Jul 5;14(13):3285. doi: 10.3390/cancers14133285.
(1) Background: SMARCB1 (INI-1)-deficient sinonasal carcinoma is a rare sinonasal malignancy; since its discovery and description in 2014, less than 200 cases have been identified. It is almost impossible to perform randomized-controlled trials on novel therapy to improve treatment outcomes in view of its rarity. We performed a systematic review of all the published case reports/series and included our patients for survival analysis. (2) Methods: In this systematic review, we searched from PubMed-MEDLINE, EMBASE, Scopus, Cochrane Library, CINAHL, and Google Scholar for individual patient data to identify and retrieve all reported SMARCB1-deficient sinonasal carcinoma. Clarification on treatment details and the most updated survival outcomes from all authors of the published case reports/series were attempted. Survival analysis for overall survival (OS) and identification of OS prognostic factors were performed. This systematic review was registered with PROSPERO (CRD42022306671). (3) Results: A total of 67 publications were identified from the systematic review and literature search. After excluding other ineligible and duplicated publications, 192 patients reported were considered appropriate for further review. After excluding duplicates and patients with incomplete pretreatment details and survival outcomes, 120 patients were identified to have a complete set of data including baseline demographics, treatment details, and survival outcomes. Together with 8 patients treated in our institution, 128 patients were included into survival analysis. After a median follow up of 17.5 months (range 0.3-149.0), 50 (46.3%) patients died. The 1-year, 2-year and 3-year OS rates were 84.3% (95% CI % 77.6-91.0), 62.9% (95% CI 53.1-72.7), and 51.8% (95% CI 40.8-62.8), respectively, and the median OS was 39.0 months (95% CI 28.5-49.5). Males ( = 0.029) and T4b disease ( = 0.013) were significant OS prognostic factors in univariable analysis, while only T4b disease ( = 0.017) remained significant in multivariable analysis. (4) Conclusions: SMARCB1-deficient sinonasal carcinoma is an extremely aggressive sinonasal malignancy with a dismal prognosis. Early diagnosis and a multimodality treatment strategy are essential for a better treatment and survival outcome.
(1) 背景:SMARCB1(INI-1)缺陷型鼻窦癌是一种罕见的鼻窦恶性肿瘤;自2014年被发现和描述以来,已确诊的病例不到200例。鉴于其罕见性,几乎不可能对新疗法进行随机对照试验以改善治疗效果。我们对所有已发表的病例报告/系列进行了系统综述,并纳入我们的患者进行生存分析。(2) 方法:在本系统综述中,我们从PubMed-MEDLINE、EMBASE、Scopus、Cochrane图书馆、CINAHL和谷歌学术搜索个体患者数据,以识别和检索所有报道的SMARCB1缺陷型鼻窦癌。试图向已发表病例报告/系列的所有作者澄清治疗细节和最新的生存结果。进行总生存(OS)的生存分析以及OS预后因素的识别。本系统综述已在PROSPERO(CRD42022306671)注册。(3) 结果:通过系统综述和文献检索共识别出67篇出版物。排除其他不符合条件和重复的出版物后,报告的192例患者被认为适合进一步审查。排除重复病例以及预处理细节和生存结果不完整的患者后,确定120例患者拥有包括基线人口统计学、治疗细节和生存结果的完整数据集。连同在我们机构接受治疗的8例患者,128例患者纳入生存分析。中位随访17.5个月(范围0.3 - 149.0个月)后,50例(46.3%)患者死亡。1年、2年和3年的OS率分别为84.3%(95%CI 77.6 - 91.0%)、62.9%(95%CI 53.1 - 72.7%)和51.8%(95%CI 40.8 - 62.8%),中位OS为39.0个月(95%CI 28.5 - 49.5个月)。单因素分析中男性(P = 0.029)和T4b期疾病(P = 0.013)是显著的OS预后因素,而多因素分析中仅T4b期疾病(P = 0.017)仍具有显著性。(4) 结论:SMARCB1缺陷型鼻窦癌是一种极具侵袭性的鼻窦恶性肿瘤,预后不佳。早期诊断和多模式治疗策略对于获得更好的治疗和生存结果至关重要。