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Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome

BACKGROUND: (18)F-FDG PET/CT provides precise information about dissemination of lymphoma lesions. Dmax, defined as distance between the two lesions that were farthest apart by PET/CT, was found to be a promising predictor of Diffuse large B-cell lymphoma (DLBCL) outcome in a small size of clinical...

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Autores principales: Wang, Fei, Cui, Silu, Lu, Luo, Shao, Xiaoliang, Yan, Feng, Liu, Yaqi, He, Bai, Wang, Jianfeng, Cao, Yang, Yue, Yanhua, Wang, Yuetao, Gu, Weiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687880/
https://www.ncbi.nlm.nih.gov/pubmed/38030989
http://dx.doi.org/10.1186/s12885-023-11333-z
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author Wang, Fei
Cui, Silu
Lu, Luo
Shao, Xiaoliang
Yan, Feng
Liu, Yaqi
He, Bai
Wang, Jianfeng
Cao, Yang
Yue, Yanhua
Wang, Yuetao
Gu, Weiying
author_facet Wang, Fei
Cui, Silu
Lu, Luo
Shao, Xiaoliang
Yan, Feng
Liu, Yaqi
He, Bai
Wang, Jianfeng
Cao, Yang
Yue, Yanhua
Wang, Yuetao
Gu, Weiying
author_sort Wang, Fei
collection PubMed
description BACKGROUND: (18)F-FDG PET/CT provides precise information about dissemination of lymphoma lesions. Dmax, defined as distance between the two lesions that were farthest apart by PET/CT, was found to be a promising predictor of Diffuse large B-cell lymphoma (DLBCL) outcome in a small size of clinical trial data. We analyzed the impact of Dmax on the outcome of a large real-world DLBCL cohort. METHODS: Data of newly diagnosed DLBCL at the Third Affiliated Hospital of Soochow University were retrospectively collected. Baseline Dmax, clinical data and survival information were recorded. A metabolic parameter, metabolic bulk volume (MBV), was also measured to verify the independent impact of Dmax. RESULTS: Optimal cut-off values for Dmax and MBV were 45.34 cm and 21.65 cm(3). With a median follow-up of 32 months, Dmax significantly impacted progression-free survival (PFS) and overall survival (OS) in 253 DLBCL patients. For Dmax(low) and Dmax(high) groups, estimated 3-year OS were 87.0% and 53.8% (p < 0.001), while 3-year PFS were 77.3% and 37.3% (p < 0.001). And for MBV(low) and MBV(high)groups, 3-year OS were 84.5% and 58.8% (p < 0.001), and 3-year PFS were 68.7% and 50.4% (p = 0.003). Multivariate analysis identified Dmax and Eastern Cooperative Oncology Group performance status (ECOG PS) independently associated with PFS and OS, while MBV only independently associated with OS. A Dmax revised prognostic index (DRPI) combining Dmax and ECOG PS identified an ultra-risk DLBCL population with 3-year PFS of 31.7% and 3-year OS of 38.5%. The area under the curve (AUC) showed that this model performed better than International prognostic Index (IPI). CONCLUSION: Dmax is a new and promising indicator to investigate dissemination of lymphoma lesions associated with the outcome of DLBCL. It significantly contributes to stratification of patients with disparate outcomes. TRIAL REGISTRATION: This research has been retrospectively registered in the Ethics Committee institutional of the Third Affiliated Hospital of Soochow University, and the registration number was approval No. 155 (approved date: 31 May 2022). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11333-z.
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spelling pubmed-106878802023-11-30 Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome Wang, Fei Cui, Silu Lu, Luo Shao, Xiaoliang Yan, Feng Liu, Yaqi He, Bai Wang, Jianfeng Cao, Yang Yue, Yanhua Wang, Yuetao Gu, Weiying BMC Cancer Research BACKGROUND: (18)F-FDG PET/CT provides precise information about dissemination of lymphoma lesions. Dmax, defined as distance between the two lesions that were farthest apart by PET/CT, was found to be a promising predictor of Diffuse large B-cell lymphoma (DLBCL) outcome in a small size of clinical trial data. We analyzed the impact of Dmax on the outcome of a large real-world DLBCL cohort. METHODS: Data of newly diagnosed DLBCL at the Third Affiliated Hospital of Soochow University were retrospectively collected. Baseline Dmax, clinical data and survival information were recorded. A metabolic parameter, metabolic bulk volume (MBV), was also measured to verify the independent impact of Dmax. RESULTS: Optimal cut-off values for Dmax and MBV were 45.34 cm and 21.65 cm(3). With a median follow-up of 32 months, Dmax significantly impacted progression-free survival (PFS) and overall survival (OS) in 253 DLBCL patients. For Dmax(low) and Dmax(high) groups, estimated 3-year OS were 87.0% and 53.8% (p < 0.001), while 3-year PFS were 77.3% and 37.3% (p < 0.001). And for MBV(low) and MBV(high)groups, 3-year OS were 84.5% and 58.8% (p < 0.001), and 3-year PFS were 68.7% and 50.4% (p = 0.003). Multivariate analysis identified Dmax and Eastern Cooperative Oncology Group performance status (ECOG PS) independently associated with PFS and OS, while MBV only independently associated with OS. A Dmax revised prognostic index (DRPI) combining Dmax and ECOG PS identified an ultra-risk DLBCL population with 3-year PFS of 31.7% and 3-year OS of 38.5%. The area under the curve (AUC) showed that this model performed better than International prognostic Index (IPI). CONCLUSION: Dmax is a new and promising indicator to investigate dissemination of lymphoma lesions associated with the outcome of DLBCL. It significantly contributes to stratification of patients with disparate outcomes. TRIAL REGISTRATION: This research has been retrospectively registered in the Ethics Committee institutional of the Third Affiliated Hospital of Soochow University, and the registration number was approval No. 155 (approved date: 31 May 2022). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11333-z. BioMed Central 2023-11-29 /pmc/articles/PMC10687880/ /pubmed/38030989 http://dx.doi.org/10.1186/s12885-023-11333-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wang, Fei
Cui, Silu
Lu, Luo
Shao, Xiaoliang
Yan, Feng
Liu, Yaqi
He, Bai
Wang, Jianfeng
Cao, Yang
Yue, Yanhua
Wang, Yuetao
Gu, Weiying
Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title_full Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title_fullStr Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title_full_unstemmed Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title_short Dissemination feature based on PET/CT is a risk factor for diffuse large B cell lymphoma patients outcome
title_sort dissemination feature based on pet/ct is a risk factor for diffuse large b cell lymphoma patients outcome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687880/
https://www.ncbi.nlm.nih.gov/pubmed/38030989
http://dx.doi.org/10.1186/s12885-023-11333-z
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