Suppr超能文献

不可切除或复发性弥漫型腱鞘巨细胞瘤(dTGCT)酪氨酸激酶抑制剂治疗的长期随访。

Long term term follow-up of tyrosine kinase inhibitors treatments in inoperable or relapsing diffuse type tenosynovial giant cell tumors (dTGCT).

机构信息

Department of Medical Oncology, Léon Bérard Cancer Center, Lyon, France.

Department of Statistics, Léon Bérard Cancer Center, Lyon, France.

出版信息

PLoS One. 2020 May 20;15(5):e0233046. doi: 10.1371/journal.pone.0233046. eCollection 2020.

Abstract

RATIONALE

CSF1R tyrosine kinase inhibitors (TKI) and antibodies yield response rates and tumor control in patients with diffuse type tenosynovial giant cell tumors (dTGCT). The long term management of patients with dTGCT treated with TKI is however not known.

PATIENTS AND METHODS

We conducted a retrospective single center study on the 39 patients with advanced and/or inoperable dTGCT referred to the Centre Leon Berard for a medical treatment. The clinical characteristics and treatments of patients who had received at least one line of CSF1R TKI or Ab was collected from the electronic patient records and analyzed, after this study was approved by the Institutional Review Board of the Centre Leon Berard. Statistics were conducted using SPSS 23.0.

RESULTS

Thirty-nine patients received at least one line of TKI among the 101 patients with histologically confirmed dTGCT refered to this center. Imatinib, nilotinib, pexidartinib, emactuzumab were the most frequently used agents. First line treatment was given for a median duration of 7 months. With a median follow-up from the initiation of TKI of 30 months, the progression-free rate at 30 months is 56% for the 39 patients. 15 patients had recurrent disease after first line CSF1R inhibitor: 12 (80%) received a 2nd line treatment for a median duration of 6 months and a median time to progression (TTP) of 12 months. Six patients had afterwards a recurrent disease and 5 (83%) received a 3rd line treatment for a median duration of 5 months and a median TTP of 9 months. Progression-free rate at 30 months was observed in 3 of 12 (25%) after line 2 and 1 of 5 (20%) after line 3. None of the patients refered died with a median follow-up of 67 months.

CONCLUSIONS

CSF1R TKI or Ab provide prolonged tumor control and symptom relief for a majority of patients with inoperable or relapsing dTGCT, in first and subsequent lines. Multiple lines are required for close to 50% of patients with relapsing dTGCT.

摘要

背景

CSF1R 酪氨酸激酶抑制剂(TKI)和抗体可使弥漫性腱鞘巨细胞瘤(dTGCT)患者的反应率和肿瘤控制率提高。然而,尚不清楚接受 TKI 治疗的 dTGCT 患者的长期管理情况。

患者和方法

我们对在莱昂贝拉德中心接受治疗的 39 例晚期和/或不可手术的 dTGCT 患者进行了回顾性单中心研究。从电子病历中收集了至少接受过一线 CSF1R TKI 或 Ab 治疗的患者的临床特征和治疗情况,并在莱昂贝拉德中心机构审查委员会批准后进行了分析。统计学分析使用 SPSS 23.0 进行。

结果

在中心就诊的 101 例组织学证实的 dTGCT 患者中,有 39 例接受了至少一线 TKI 治疗。伊马替尼、尼洛替尼、培昔替尼、埃马曲珠单抗是最常使用的药物。一线治疗的中位持续时间为 7 个月。从 TKI 开始的中位随访时间为 30 个月,39 例患者的 30 个月无进展生存率为 56%。一线 CSF1R 抑制剂治疗后,15 例患者出现疾病复发:12 例(80%)接受二线治疗,中位持续时间为 6 个月,中位进展时间(TTP)为 12 个月。6 例患者随后出现疾病复发,其中 5 例(83%)接受三线治疗,中位持续时间为 5 个月,中位 TTP 为 9 个月。二线治疗后 30 个月无进展生存率为 12 例中的 3 例(25%),三线治疗后 5 例中的 1 例(20%)。中位随访 67 个月时,无患者死亡。

结论

CSF1R TKI 或 Ab 可为大多数不可手术或复发的 dTGCT 患者提供延长的肿瘤控制和症状缓解,无论是一线还是后续治疗。对于近 50%的复发 dTGCT 患者,需要多线治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验