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范可尼贫血行造血干细胞移植后继发舌癌

Tongue cancer following hematopoietic cell transplantation for Fanconi anemia.

机构信息

Surgery, Dentistry, Maternity and Infant Department, Unit of Dentistry and Maxillo-Facial Surgery, University of Verona, P.le L.A. Scuro 10, 37134, Verona, Italy.

Department of Medical and Surgical Sciences for Children & Adults, Cranio-Maxillo-Facial Surgery, University of Modena and Reggio Emilia, Largo del Pozzo 71, 41124, Modena, Italy.

出版信息

Clin Oral Investig. 2022 Sep;26(9):5943-5952. doi: 10.1007/s00784-022-04554-2. Epub 2022 May 28.

Abstract

OBJECTIVES

The aim of this retrospective study was to determine the incidence and the clinical outcome of tongue cancer (TC) in patients affected by Fanconi anemia (FA) who received an allogeneic hematopoietic cell transplantation (HCT).

MATERIALS AND METHODS

The patient database from the Bone Marrow Transplant Center of Pescara was reviewed to enroll FA patients. Patients', donors', HCT's, and screening's data were collected as well to look for the incidence and the treatment of TC.

RESULTS

Twelve patients affected by FA were identified. Three patients died for transplant-related causes. Five of nine surviving patients were diagnosed with TC at a median of 21.7 years since transplantation and at a median age of 32.10 years. Interestingly, no patient manifested graft-versus-host-disease (GvHD). The 28-year cumulative incidence function of TC was 46.9% (95% CI, 36.9-56.9%). Two patients were treated with chemotherapy alone, two patients were treated with surgery alone, and one with surgery followed by chemotherapy. Overall, 4 patients with TC showed a clinical course characterized by a marked aggressiveness of the tumor disease which led to death due to cancer progression between 2 and 13 months. One patient is surviving 8 months after diagnosis of TC.

CONCLUSIONS

Our study confirms the high incidence of tumors and in particular tongue tumors in allotransplanted FA patients. A careful screening has to be life-long maintained.

CLINICAL RELEVANCE

Considering the rarity of FA and the frailty of FA patients, this study may add important information for the cancer management of these patients.

摘要

目的

本回顾性研究旨在确定接受异基因造血细胞移植(HCT)的范可尼贫血(FA)患者中舌癌(TC)的发病率和临床结局。

材料和方法

审查了佩斯卡拉骨髓移植中心的患者数据库,以招募 FA 患者。收集了患者、供者、HCT 和筛查的数据,以寻找 TC 的发病率和治疗方法。

结果

确定了 12 名患有 FA 的患者。3 名患者因移植相关原因死亡。9 名存活患者中有 5 名在移植后中位时间 21.7 年且中位年龄 32.10 岁时被诊断为 TC。有趣的是,没有患者出现移植物抗宿主病(GvHD)。TC 的 28 年累积发病率函数为 46.9%(95%CI,36.9-56.9%)。2 名患者单独接受化疗,2 名患者单独接受手术,1 名患者先手术后化疗。总的来说,4 名 TC 患者的肿瘤疾病具有明显侵袭性,导致 2 至 13 个月内因癌症进展而死亡。1 名患者在诊断为 TC 后存活 8 个月。

结论

我们的研究证实了 FA 患者接受同种异体移植后肿瘤发病率高,特别是舌肿瘤发病率高。必须终身进行仔细筛查。

临床相关性

考虑到 FA 的罕见性和 FA 患者的脆弱性,这项研究可能为这些患者的癌症管理提供重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/9474471/18046545c060/784_2022_4554_Fig1_HTML.jpg

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