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局部晚期鼻咽癌中高危患者大剂量顺铂化疗的疗效。

Efficiency of high cumulative cisplatin dose in high- and low-risk patients with locoregionally advanced nasopharyngeal carcinoma.

机构信息

Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.

Department of Oncology, Affiliated Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

Cancer Med. 2022 Feb;11(3):715-727. doi: 10.1002/cam4.4477. Epub 2021 Dec 3.

DOI:10.1002/cam4.4477
PMID:34859600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8817101/
Abstract

BACKGROUND

The optimal cumulative cisplatin dose (CCD) during radiation therapy for locoregionally advanced nasopharyngeal carcinoma (LA-NPC) patients receiving induction chemotherapy (IC) plus CCRT remains controversial. This study aimed to explore the treatment efficiency of CCD for high-and low-risk patients with LA-NPC.

METHODS

Data from 472 LA-NPC patients diagnosed from 2014 to 2018 and treated with IC plus CCRT were reviewed. After propensity score matching, the therapeutic effects of a CCD > 200 and CCD ≤ 200 mg/m were evaluated comparatively. Five factors selected by multivariate analysis were incorporated to develop a nomogram. Subgroup analysis was conducted to explore the role of different CCDs in nomogram-defined high- and low-risk groups. Additionally, acute toxicities were evaluated comparatively between the high- and low-CCD groups.

RESULTS

After matching, there was no difference between different CCD groups for all patients in terms of 3-year overall survival (OS), distant metastasis-free survival (DMFS), locoregional recurrence-free survival (LRRFS), or progression-free survival (PFS). A nomogram was built by integrating pretreatment EBV DNA, clinical stage, and post-IC EBV DNA, post-IC primary gross tumor and lymph node volumes obtained a C-index of 0.674. The high-risk group determined by the nomogram had poorer 3-year PFS, OS, DMFS, and LRRFS than the low-risk group. A total of CCD > 200 mg/m increased the survival rates of 3-year PFS and DMFS (PFS: 72.5% vs. 54.4%, p = 0.012; DMFS: 81.9% vs. 61.5%, p = 0.014) in the high-risk group but not in the low-risk group. Moreover, the high CCD increased treatment-related acute toxicities.

CONCLUSIONS

A high CCD was associated with better 3-year PFS and DMFS rates than a low dose for high-risk patients but could not produce a survival benefit for low-risk patients.

摘要

背景

接受诱导化疗(IC)加同期放化疗(CCRT)的局部晚期鼻咽癌(LA-NPC)患者,其放射治疗过程中最佳累积顺铂剂量(CCD)仍存在争议。本研究旨在探讨 CCD 对 LA-NPC 高危和低危患者的治疗效果。

方法

回顾性分析 2014 年至 2018 年间诊断为 LA-NPC 并接受 IC 加 CCRT 治疗的 472 例患者的数据。经倾向性评分匹配后,比较 CCD>200mg/m 和 CCD≤200mg/m 的治疗效果。采用多因素分析选择的 5 个因素构建列线图。进行亚组分析以探讨不同 CCD 在列线图定义的高危和低危组中的作用。此外,还比较了高低 CCD 组之间的急性毒性。

结果

匹配后,对于所有患者,不同 CCD 组之间的 3 年总生存率(OS)、无远处转移生存率(DMFS)、无局部区域复发生存率(LRRFS)和无进展生存率(PFS)均无差异。通过整合治疗前 EBV DNA、临床分期、IC 后 EBV DNA、IC 后原发肿瘤和淋巴结体积,构建了一个 C 指数为 0.674 的列线图。该列线图确定的高危组的 3 年 PFS、OS、DMFS 和 LRRFS 均低于低危组。对于高危组,总 CCD>200mg/m 可提高 3 年 PFS 和 DMFS 生存率(PFS:72.5% vs. 54.4%,p=0.012;DMFS:81.9% vs. 61.5%,p=0.014),但在低危组中无此作用。此外,高 CCD 增加了与治疗相关的急性毒性。

结论

对于高危患者,高 CCD 与 3 年 PFS 和 DMFS 率的提高相关,但对于低危患者,不能产生生存获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/e23fc360df3b/CAM4-11-715-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/716e6dc5f87f/CAM4-11-715-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/c26cc43f5b8f/CAM4-11-715-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/b7dcdc776460/CAM4-11-715-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/e23fc360df3b/CAM4-11-715-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/716e6dc5f87f/CAM4-11-715-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/c26cc43f5b8f/CAM4-11-715-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/b7dcdc776460/CAM4-11-715-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/8817101/e23fc360df3b/CAM4-11-715-g002.jpg

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