The Impact of Focal Lesions on Overall and Progression-free Survival in Multiple Myeloma.

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Indian Journal of Nuclear Medicine Pub Date : 2024-09-01 Epub Date: 2025-01-25 DOI:10.4103/ijnm.ijnm_131_24
Tugcan Alp Kirkizlar, Onur Kirkizlar, Selin Soyluoglu, Elif Gulsum Umit, Funda Ustun, Ahmet Muzaffer Demir
{"title":"The Impact of Focal Lesions on Overall and Progression-free Survival in Multiple Myeloma.","authors":"Tugcan Alp Kirkizlar, Onur Kirkizlar, Selin Soyluoglu, Elif Gulsum Umit, Funda Ustun, Ahmet Muzaffer Demir","doi":"10.4103/ijnm.ijnm_131_24","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>In this study, we aimed to reveal the incidence of ≥3 focal lesions (FLs) and analyze overall survival (OS) and progression-free survival (PFS) according to the number of FLs, as well as to identify mortality and PFS risk factors, in our newly diagnosed multiple myeloma (NDMM) patients.</p><p><strong>Materials and methods: </strong>A total of 89 NDMM patients who underwent <sup>18</sup>F-FDG positron emission tomography/computerized tomography (PET/CT) imaging were included in the study.</p><p><strong>Results: </strong>While 57.3% of the patients had ≥3 FLs, 20.2% had no FL. The median OS and PFS were 55 and 43 months, respectively. The median survival time was 49 months for patients with ≥3 FLs and 101 months for patients with <3 FLs, with a statistically significant difference (<i>P</i> = 0.049). The median PFS was 34 months in patients with ≥3 FLs and 67 months in patients with <3 FLs; this difference was also statistically significant (<i>P</i> = 0.026). The difference in median survival was statistically significant, based on whether autologous stem cell transplantation (ASCT) was performed and the number of FLs (≥3 or <3) (<i>P</i> = 0.011). In the multivariate regression analysis, ≥3 FLs was not a predictor of mortality but was a risk factor for PFS.</p><p><strong>Conclusion: </strong>In our study, we observed significantly worse OS and PFS in patients with ≥3 FLs at diagnosis, and it is noteworthy that the OS was worse in those patients who did not undergo ASCT. <sup>18</sup>F-FDG PET/CT is a feasible imaging technique for the prediction of prognosis in the initial evaluation of NDMM, and we believe that consolidation with ASCT as a modifiable factor, especially in patients with ≥3 FLs, will lead to a more favorable prognosis.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"39 5","pages":"353-359"},"PeriodicalIF":0.5000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11884343/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Nuclear Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijnm.ijnm_131_24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/25 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: In this study, we aimed to reveal the incidence of ≥3 focal lesions (FLs) and analyze overall survival (OS) and progression-free survival (PFS) according to the number of FLs, as well as to identify mortality and PFS risk factors, in our newly diagnosed multiple myeloma (NDMM) patients.

Materials and methods: A total of 89 NDMM patients who underwent 18F-FDG positron emission tomography/computerized tomography (PET/CT) imaging were included in the study.

Results: While 57.3% of the patients had ≥3 FLs, 20.2% had no FL. The median OS and PFS were 55 and 43 months, respectively. The median survival time was 49 months for patients with ≥3 FLs and 101 months for patients with <3 FLs, with a statistically significant difference (P = 0.049). The median PFS was 34 months in patients with ≥3 FLs and 67 months in patients with <3 FLs; this difference was also statistically significant (P = 0.026). The difference in median survival was statistically significant, based on whether autologous stem cell transplantation (ASCT) was performed and the number of FLs (≥3 or <3) (P = 0.011). In the multivariate regression analysis, ≥3 FLs was not a predictor of mortality but was a risk factor for PFS.

Conclusion: In our study, we observed significantly worse OS and PFS in patients with ≥3 FLs at diagnosis, and it is noteworthy that the OS was worse in those patients who did not undergo ASCT. 18F-FDG PET/CT is a feasible imaging technique for the prediction of prognosis in the initial evaluation of NDMM, and we believe that consolidation with ASCT as a modifiable factor, especially in patients with ≥3 FLs, will lead to a more favorable prognosis.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
局灶性病变对多发性骨髓瘤患者总体生存和无进展生存的影响。
目的:本研究旨在揭示新诊断的多发性骨髓瘤(NDMM)患者≥3个局灶性病变(FLs)的发生率,并根据FLs数量分析总生存期(OS)和无进展生存期(PFS),并确定死亡率和PFS的危险因素。材料与方法:89例行18F-FDG正电子发射断层扫描/ PET/CT扫描的NDMM患者纳入研究。结果:57.3%的患者有≥3个FL, 20.2%的患者没有FL,中位OS和PFS分别为55和43个月。≥3个FLs的患者中位生存时间为49个月,P = 0.049的患者中位生存时间为101个月。≥3个FLs患者的中位PFS为34个月,P = 0.026的患者为67个月。基于是否进行自体干细胞移植(ASCT)和FLs数量,中位生存期差异具有统计学意义(≥3或P = 0.011)。在多变量回归分析中,≥3 FLs不是死亡率的预测因子,但却是PFS的危险因素。结论:在我们的研究中,我们观察到诊断时≥3个FLs的患者的OS和PFS明显更差,值得注意的是,未行ASCT的患者的OS更差。18F-FDG PET/CT在NDMM的初步评估中是一种可行的预测预后的影像学技术,我们认为ASCT巩固作为一种可改变的因素,特别是对于≥3 FLs的患者,将会导致更有利的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Indian Journal of Nuclear Medicine
Indian Journal of Nuclear Medicine RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
0.70
自引率
0.00%
发文量
46
期刊最新文献
18F-FDG PET/CT in a Rare Case of Multiple Parasitic Leiomyomas after Laparoscopic Morcellation. Brown fat FDG Uptake - A Common Finding in FDG PET CT Scan and the Relation to Demographic, Environmental, and Clinical Factors. Comparison of FDOPA and FDG PET in Parkinson's Disease Patients with and without Freezing of Gait. Gastric Adenocarcinoma with Bone Marrow Metastasis. 18F-FDG PET/CT in Lung Hepatoid Adenocarcinoma.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1