Advanced Search
Turn off MathJax
Article Contents
LI Hui, JIANCHENG Li, FENG Liu, DI Wu, CHUANBEN Chen, JINLUAN Li. A Novel Prognostic Model Establishment and Treatment Efficacy Analysis for Primary Pulmonary Non-Hodgkin’s Lymphoma[J]. Journal of Electronics & Information Technology. doi: 10.11999/JEIT250874
Citation: LI Hui, JIANCHENG Li, FENG Liu, DI Wu, CHUANBEN Chen, JINLUAN Li. A Novel Prognostic Model Establishment and Treatment Efficacy Analysis for Primary Pulmonary Non-Hodgkin’s Lymphoma[J]. Journal of Electronics & Information Technology. doi: 10.11999/JEIT250874

A Novel Prognostic Model Establishment and Treatment Efficacy Analysis for Primary Pulmonary Non-Hodgkin’s Lymphoma

doi: 10.11999/JEIT250874 cstr: 32379.14.JEIT250874
Funds:  Fujian Research and Training Grants for Youth and Middle-aged Leaders in Healthcare, 2022, Natural Science Foundation of Fujian Province, 2025J01221, Fujian Provincial Clinical Research Center for Cancer Radiotherapy and Immunotherapy, 2020Y2012
  • Received Date: 2025-08-31
  • Accepted Date: 2026-01-22
  • Rev Recd Date: 2026-01-22
  • Available Online: 2026-03-04
  •   Objective  At present, there are few related studies on primary pulmonary non-Hodgkin's lymphoma (PPL), mainly single-center and retrospective studies. Therefore, there is no widely used and recognized prognostic index and treatment decision for PPL. This study aims to establish and verify a novel International Prognostic Index (IPI) of PPL by using the data of cancer population in the United States and Chinese multi-centers, and to compare the curative effects of different treatment methods. So as to predict the clinical prognosis and to provide new and effective ideas for making treatment decisions of PPL.  Methods  In this study, the clinical data of patients diagnosed with PPL from 2000 to 2019 in the Surveillance, Epidemiology, and End Results (SEER) database of America and from 2010 to 2021 in 3 tertiary hospitals in China were included. Cox proportional hazards regression model was used to determine independent prognostic factors and a nomogram was established to predict cancer-specific survival (CSS). The model was validated using the Concordance-index (C-index) and calibration curve. Combining nomogram with IPI, a novel prognostic index was established, risk stratified and the 3-year overall survival (OS) rate was calculated. The inverse probability of treatment weighting (IPTW) was used to eliminate confounding factors, and Kaplan-Meier curve and Log-rank test were used for survival analysis.  Results and Discussions  Finally, a total of 4,313 cases from the SEER database and 107 cases from the Chinese multi-center were included this study. The multivariate Cox regression results showed that the independent prognostic factors of PPL included age (P<0.001; hazard ratio [HR], 1.078; 95% confidence interval [CI], 1.072–1.084), Ann Arbor stage (P<0.001), sex (P<0.001; HR, 0.719; 95% CI, 0.624–0.829), primary site (P=0.037), pathological type (P<0.001), B symptom (p=0.012; HR, 0.944; 95% CI, 0.773–0.997), surgery (P<0.001; HR, 1.453; 95% CI, 1.221–1.728), chemotherapy (P<0.001; HR, 0.742; 95% CI, 0.631–0.872), marital status (P<0.001). Based on these independent prognostic factors, a nomogram with 3, 5, and 10 years of CSS was established. By combining nomogram and IPI, we established a prognostic model of PPL, and its C-index was 0.932. By defining risk factors and stratifying the model, we established a novel prognostic index for PPL. The risk parameters were defined as: age > 60 years, Ann Arbor stage III/IV, serum LDH level >1 times normal level, performance status score >2, number of extranodal invasion >1, male, except mucosa-associated lymphoid tissue (MALT), positive B symptoms, and not receive cancer therapy; the definition of risk stratification and their 3-year OS rate were: low-risk group (0-2 risk factors) 96.97%, low-mediate risk group (3-4 risk factors) 82.61%, high-mediate risk group (5 risk factors) 50%, and high risk group (6-9 risk factors) 11.11%, (P<0.001). Regarding the efficacy comparison of treatment methods, both the American and Chinese data showed that chemotherapy significantly reduced the CSS of patients with primary pulmonary MALT lymphoma (P<0.001). There were no significant differences between the efficacy of surgery and radiotherapy both in primary pulmonary MALT lymphoma and diffuse large B-cell lymphoma (P>0.05).  Conclusions  First, this study established a novel prognostic index for PPL based on the data of the American cancer population and the Chinese multi-center cohort. The parameters were age, stage, serum LDH level, performance status score, and numbers of extranodal invasion. The index has excellent predictive ability and accuracy. Through risk stratification of this index, the 3-year OS rate of different risk groups were obtained. Finally, the efficacy analysis suggested that chemotherapy may be detrimental the CSS of patients with primary pulmonary MALT lymphoma. In addition, there was no significant difference of surgery and radiotherapy both in primary pulmonary MALT lymphoma and diffuse large B-cell lymphoma.
  • loading
  • [1]
    SIEGEL R L, MILLER K D, FUCHS H E, et al. Cancer statistics, 2022[J]. CA: A Cancer Journal for Clinicians, 2022, 72(1): 7–33. doi: 10.3322/caac.21708.
    [2]
    SMALL W. Perez and brady’s principles and practice of radiation oncology[J]. JAMA, 2009, 301(19): 2046–2051. doi: 10.1001/jama.2009.718.
    [3]
    GIZA A, DUMNICKA P, KALICIŃSKA E, et al. Retrospective analysis of primary pulmonary lymphoma cases from Polish Lymphoma Research Group centers reveals associations between initial symptoms and outcomes[J]. Scientific Reports, 2025, 15(1): 27883. doi: 10.1038/s41598-025-12469-7.
    [4]
    PDQ Pediatric Treatment Editorial Board. Childhood non-hodgkin lymphoma treatment (PDQ®)-Health professional version[R]. Bethesda: National Cancer Institute, 2002.
    [5]
    SMYTH R, SLOAN J M, BURKS E, et al. Primary pulmonary marginal zone lymphoma: An unusual cause of pulmonary infiltrates[J]. Respirology Case Reports, 2021, 9(8): e00806. doi: 10.1002/rcr2.806.
    [6]
    DONG Congsong, XIA Peng, QIU Wenli, et al. Evaluation of CT features for differentiating consolidation pattern of pulmonary MALT lymphoma from pneumonic-type lung adenocarcinoma[J]. Frontiers in Oncology, 2023, 13: 1234291. doi: 10.3389/fonc.2023.1234291.
    [7]
    The International Non-Hodgkin's Lymphoma Prognostic Factors Project. A predictive model for aggressive non-Hodgkin’s lymphoma[J]. The New England Journal of Medicine, 1993, 329(14): 987–994. doi: 10.1056/NEJM199309303291402.
    [8]
    HE Xiaoyu, HUANG Qian, LI Wenqiang, et al. Prognostic factors and predictive models for primary pulmonary diffuse large B-cell lymphoma: A population-based analysis[J]. Hematology, 2024, 29(1): 2420160. doi: 10.1080/16078454.2024.2420160.
    [9]
    THIEBLEMONT C, CASCIONE L, CONCONI A, et al. A MALT lymphoma prognostic index[J]. Blood, 2017, 130(12): 1409–1417. doi: 10.1182/blood-2017-03-771915.
    [10]
    KIM H D, CHO H, JEONG H, et al. A prognostic index for extranodal marginal-zone lymphoma based on the mucosa-associated lymphoid tissue International Prognostic Index and serum β2-microglobulin levels[J]. British Journal of Haematology, 2021, 193(2): 307–315. doi: 10.1111/bjh.17222.
    [11]
    SHEN Hui and ZHOU Yaodong. Clinical features and surgical treatment of primary pulmonary lymphoma: A retrospective study[J]. Frontiers in Oncology, 2022, 12: 779395. doi: 10.3389/fonc.2022.779395.
    [12]
    NING Ye, HE Haiyan, LI Qiuyuan, et al. The prognosis of patients with primary pulmonary mucosa-associated lymphoid tissue lymphoma: Treated with surgery or chemotherapy?[J]. European Journal of Cardio-Thoracic Surgery, 2024, 65(3): ezae064. doi: 10.1093/ejcts/ezae064.
    [13]
    VANDEN EYNDEN F, FADEL E, DE PERROT M, et al. Role of surgery in the treatment of primary pulmonary B-cell lymphoma[J]. The Annals of Thoracic Surgery, 2007, 83(1): 236–240. doi: 10.1016/j.athoracsur.2006.08.026.
    [14]
    ABRISQUETA P. New insights into first-line therapy in diffuse large B-cell lymphoma: Are we improving outcomes?[J]. Journal of Clinical Medicine, 2024, 13(7): 1929. doi: 10.3390/jcm13071929.
    [15]
    JELICIC J, JUUL-JENSEN K, BUKUMIRIC Z, et al. Prognostic indices in diffuse large B-cell lymphoma: A population-based comparison and validation study of multiple models[J]. Blood Cancer Journal, 2023, 13(1): 157. doi: 10.1038/s41408-023-00930-7.
    [16]
    CLAVIJO N D, AGUIRRE J C F, DEL PILAR AGUDELO LOPEZ C, et al. Aligning outcomes: DLBCL prognosis at a 4th Level University Hospital in Bogotá is comparable to high-income nations, identification of additional prognostic markers for overall survival and relapse[J]. Ecancermedicalscience, 2024, 18: 1717. doi: 10.3332/ecancer.2024.1717.
    [17]
    PENCINA M J and D'AGOSTINO R B. Overall C as a measure of discrimination in survival analysis: Model specific population value and confidence interval estimation[J]. Statistics in Medicine, 2004, 23(13): 2109–2123. doi: 10.1002/sim.1802.
    [18]
    KAMMULA A V, SCHÄFFER A A, RAJAGOPAL P S, et al. Outcome differences by sex in oncology clinical trials[J]. Nature Communications, 2024, 15(1): 2608. doi: 10.1038/s41467-024-46945-x.
    [19]
    KISERUD C E, SCHOVER L R, DAHL A A, et al. Do male lymphoma survivors have impaired sexual function?[J]. Journal of Clinical Oncology, 2009, 27(35): 6019–6026. doi: 10.1200/JCO.2009.23.2280.
    [20]
    SOLAL-CÉLIGNY P, ROY P, COLOMBAT P, et al. Follicular lymphoma international prognostic index[J]. Blood, 2004, 104(5): 1258–1265. doi: 10.1182/blood-2003-12-4434.
    [21]
    O'REILLY S E and CONNORS J M. Non-Hodgkin's lymphoma. I: Characterisation and treatment[J]. British Medical Journal, 1992, 304(6843): 1682–1686. doi: 10.1136/bmj.304.6843.1682.
    [22]
    RADERER M, KIESEWETTER B, and FERRERI A J M. Clinicopathologic characteristics and treatment of marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma)[J]. CA: A Cancer Journal for Clinicians, 2016, 66(2): 153–171. doi: 10.3322/caac.21330.
    [23]
    CADRANEL J, WISLEZ M, and ANTOINE M. Primary pulmonary lymphoma[J]. European Respiratory Journal, 2002, 20(3): 750–762. doi: 10.1183/09031936.02.00404102.
    [24]
    GRAHAM B B, MATHISEN D J, MARK E J, et al. Primary pulmonary lymphoma[J]. The Annals of Thoracic Surgery, 2005, 80(4): 1248–1253. doi: 10.1016/j.athoracsur.2005.04.014.
    [25]
    ZUCCA E and CAVALLI F. Extranodal lymphomas[J]. Annals of Oncology, 2000, 11(S3): 219–222. doi: 10.1093/annonc/11.suppl_3.219.
    [26]
    WANG Haotian, ZHANG Ying, LI Zhaoxia, et al. Characteristics, efficacy, and prognosis analysis of newly diagnosed marginal zone lymphoma[J]. Frontiers in Immunology, 2024, 15: 1466859. doi: 10.3389/fimmu.2024.1466859.
    [27]
    ZIEPERT M, HASENCLEVER D, KUHNT E, et al. Standard international prognostic index remains a valid predictor of outcome for patients with aggressive CD20+ B-cell lymphoma in the rituximab era[J]. Journal of Clinical Oncology, 2010, 28(14): 2373–2380. doi: 10.1200/JCO.2009.26.2493.
    [28]
    SEHN L H and GASCOYNE R D. Diffuse large B-cell lymphoma: Optimizing outcome in the context of clinical and biologic heterogeneity[J]. Blood, 2015, 125(1): 22–32. doi: 10.1182/blood-2014-05-577189.
    [29]
    MAZLOOM A, MEDEIROS L J, MCLAUGHLIN P W, et al. Marginal zone lymphomas: Factors that affect the final outcome[J]. Cancer, 2010, 116(18): 4291–4298. doi: 10.1002/cncr.25325.
    [30]
    PARRY-JONES N, MATUTES E, GRUSZKA-WESTWOOD A M, et al. Prognostic features of splenic lymphoma with villous lymphocytes: A report on 129 patients[J]. British Journal of Haematology, 2003, 120(5): 759–764. doi: 10.1046/j.1365-2141.2003.04165.x.
    [31]
    ZHOU Zheng, SEHN L H, RADEMAKER A W, et al. An enhanced International Prognostic Index (NCCN-IPI) for patients with diffuse large B-cell lymphoma treated in the rituximab era[J]. Blood, 2014, 123(6): 837–842. doi: 10.1182/blood-2013-09-524108.
    [32]
    ZELENETZ A D, GORDON L I, CHANG J E, et al. NCCN Guidelines® insights: B-cell lymphomas, version 5.2021[J]. Journal of the National Comprehensive Cancer Network, 2021, 19(11): 1218–1230. doi: 10.6004/jnccn.2021.0054.
    [33]
    TIAN Zhizhong, LIU Linxia, WU Lijuan, et al. Correction: Enhancement of vitamin B6 production driven by omics analysis combined with fermentation optimization[J]. Microbial Cell Factories, 2024, 23(1): 257. doi: 10.1186/s12934-024-02532-9.
    [34]
    PINOTTI G, ZUCCA E, ROGGERO E, et al. Clinical features, treatment and outcome in a series of 93 patients with low-grade gastric MALT lymphoma[J]. Leukemia & Lymphoma, 1997, 26(5/6): 527–537. doi: 10.3109/10428199709050889.
    [35]
    THIEBLEMONT C, DUMONTET C, BOUAFIA F, et al. Outcome in relation to treatment modalities in 48 patients with localized gastric MALT lymphoma: A retrospective study of patients treated during 1976-2001[J]. Leukemia & Lymphoma, 2003, 44(2): 257–262. doi: 10.1080/1042819021000035680.
    [36]
    LIAO Qiuling, YU Qilin, YU Cheng, et al. Pulmonary mucosa-associated lymphoid tissue lymphoma: Insights from a 15-year study at a single institution involving 14 clinical cases[J]. World Journal of Surgical Oncology, 2024, 22(1): 219. doi: 10.1186/s12957-024-03500-8.
    [37]
    ZUCCA E and BERTONI F. The spectrum of MALT lymphoma at different sites: Biological and therapeutic relevance[J]. Blood, 2016, 127(17): 2082–2092. doi: 10.1182/blood-2015-12-624304.
    [38]
    TSANG R W and GOSPODAROWICZ M K. Radiation therapy for localized low-grade non-Hodgkin's lymphomas[J]. Hematological Oncology, 2005, 23(1): 10–17. doi: 10.1002/hon.743.
    [39]
    WÖHRER S, TROCH M, STREUBEL B, et al. MALT lymphoma in patients with autoimmune diseases: A comparative analysis of characteristics and clinical course[J]. Leukemia, 2007, 21(8): 1812–1818. doi: 10.1038/sj.leu.2404782.
    [40]
    BORIE R, WISLEZ M, ANTOINE M, et al. Lymphoproliferative disorders of the lung[J]. Respiration, 2017, 94(2): 157–175. doi: 10.1159/000477740.
    [41]
    ARMSTRONG P, HAYDEN P, JEFFERS M, et al. Pulmonary mucosa-associated lymphoid tissue lymphoma treated with radiation therapy: A case report and review of the literature[J]. Case Reports in Oncology, 2023, 16(1): 1528–1535. doi: 10.1159/000534802.
    [42]
    SANGUEDOLCE F, ZANELLI M, ZIZZO M, et al. Primary pulmonary B-cell lymphoma: A review and update[J]. Cancers, 2021, 13(3): 415. doi: 10.3390/cancers13030415.
    [43]
    FERRARO P, TRASTEK V F, ADLAKHA H, et al. Primary non-Hodgkin's lymphoma of the lung[J]. The Annals of Thoracic Surgery, 2000, 69(4): 993–997. doi: 10.1016/s0003-4975(99)01535-0.
    [44]
    REZAZADEH A, SZABO A, KHURANA A, et al. Outcomes of limited stage primary bone diffuse large B-cell lymphoma in the rituximab era: A multicenter, retrospective study[J]. Haematologica, 2024, 109(5): 1439–1444. doi: 10.3324/haematol.2023.283210.
    [45]
    KIEŁBOWSKI K, KORDYKIEWICZ D, JESIONKA J, et al. A rare case of primary pulmonary diffuse large B-cell lymphoma transformed from marginal zone mucosa-associated lymphoid tissue lymphoma[J]. Medicina, 2024, 60(6): 840. doi: 10.3390/medicina60060840.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(4)  / Tables(3)

    Article Metrics

    Article views (25) PDF downloads(1) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return