Comparison of clinical and MRI features of brain metastases between ALK plus and ALK- NSCLC

被引:0
|
作者
Ren, Xiaolu [1 ]
Zhang, Xuting [2 ]
Lei, Xiaoyan [3 ]
Ma, Weiqin [3 ]
Zhang, Ting [2 ]
Wang, Yuxiang [4 ]
Ren, Jiwei [2 ]
机构
[1] Shanxi Med Univ, Dept Radiotherapy, Shanxi Prov Canc Hosp, Shanxi Hosp,Canc Hosp,Chinese Acad Med Sci, Taiyuan, Shanxi, Peoples R China
[2] Shanxi Med Univ, Dept Radiol, Shanxi Prov Canc Hosp, Shanxi Hosp,Canc Hosp,Chinese Acad Med Sci, 3 New Workers Rd, Taiyuan 030013, Shanxi, Peoples R China
[3] Shanxi Med Univ, Inst Med Imaging, Taiyuan, Shanxi, Peoples R China
[4] Shanxi Med Univ, Dept Ultrasound, Shanxi Prov Canc Hosp, Shanxi Hosp,Canc Hosp,Chinese Acad Med Sci, 3 New Workers Rd, Taiyuan 030013, Shanxi, Peoples R China
来源
CANCER MEDICINE | 2024年 / 13卷 / 11期
基金
山西省青年科学基金;
关键词
anaplastic lymphoma kinase; brain metastases; MRI; nomogram; NSCLC; radiotherapy; CELL LUNG-CANCER; MUTATION STATUS; INHIBITORS; TUMORS; EGFR;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Non-small-cell lung cancer (NSCLC) is the primary cause of brain metastases (BM). This study aimed to investigate differences in clinical and magnetic resonance imaging (MRI) features of BM between anaplastic lymphoma kinase (ALK) gene fusion (ALK+) and ALK wild-type (ALK-) NSCLC, and to preliminarily assess the efficacy of radiotherapy for treating BM. Methods: A retrospective analysis included 101 epidermal growth factor receptor (EGFR)- NSCLC patients with BM: 41 with ALK gene fusion and 60 being ALK-. The brain MRI and clinical features were compared between different ALK status using the multivariate analysis, and a nomogram was constructed to predict ALK gene fusion. Fifty-six patients who did not undergo cerebral surgery and had complete pre- and post- treatment data were further divided based on whether they received radiotherapy. Log-rank test was used to compare the short-term effect of treatment between the two groups under different genotypes. Results: ALK+ BM exhibited decreased peritumoral brain edema size, lower peritumoral brain edema index (PBEI), and a more homogeneous contrast enhancement pattern compared to ALK- BM. Age (OR = 1.04; 95%CI: 1.02-1.06), time to BM (OR = 1.50; 95% CI: 1.04-2.14), PBEI (OR = 1.26; 95% CI: 0.97-1.62), smoking status (smoking index >400 vs. non-smoking status: OR = 1.42; 95% CI: 0.99-2.04) and contrast enhancement pattern (OR = 1.89; 95% CI: 1.28-2.78) were associated with ALK gene fusion. A nomogram based on these variables demonstrated acceptable predictive efficiency (AUC = 0.844). In the ALK+ group, patients who received radiotherapy did not show increased disease control rate (DCR) or progression-free survival (PFS). In contrast, in the ALK- group, those who received radiotherapy had improved objective response rate (ORR), DCR, and PFS compared to those who were only treated with systemic therapy. Conclusions: The clinical and MRI features of BM can indicate the status of ALK in NSCLC. In the ALK- group, patients who received radiotherapy showed higher ORR, DCR, and PFS compared to those who did not.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Analysis of clinical characteristics and outcomes of ALK positive (ALK plus ) patients treated with ALK inhibitors (ALKi).
    Perez, Susana Cedres
    Aranda, Nuria Pardo
    Navarro, Alejandro
    Marti, Alex Martinez
    de Castro, Ana Maria Martinez
    Cabrera, Guadalupe
    Vilaro, Marta
    Carbonell, LLuisa
    de la Fuente, Iris
    Piera, Adelaida
    Martinez, Lidia
    Hernandez-Losa, Javier
    Sansano, Irene
    Felip, Enriqueta
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [42] Experience from the ASCEND-1 trial: Ceritinib in patients (Pts) with ALK-rearranged (ALK plus ) Non-Small Cell Lung Cancer (NSCLC) and brain metastases
    Thomas, M.
    Schuler, M.
    Potzner, M.
    Szczudlo, T.
    Sutradhar, S.
    Yovine, A.
    Wolf, J.
    Oncology Research and Treatment, 2015, 38 : 270 - 270
  • [43] EVALUATION OF ANAPLASTIC LYMPHOMA KINASE (ALK) INHIBITOR BRIGATINIB [AP26113] IN PATIENTS (PTS) WITH ALK plus NON-SMALL CELL LUNG CANCER (NSCLC) AND BRAIN METASTASES
    Kerstein, D.
    Gettinger, S.
    Gold, K.
    Langer, C. J.
    Shaw, A. T.
    Bazhenova, L. A.
    Salgia, R.
    Dorer, D. J.
    Conlan, M. G.
    Camidge, D. R.
    ANNALS OF ONCOLOGY, 2015, 26
  • [44] ALK Genomic Aberrations in NSCLC and Clinical Implications
    Hirsch, F. R.
    JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (11) : S1163 - S1164
  • [45] Prospective screening for ALK: Clinical features and outcome according to ALK status
    Fallet, Vincent
    Cadranel, Jacques
    Doubre, Helene
    Toper, Cecile
    Monnet, Isabelle
    Chinet, Thierry
    Oliviero, Gerard
    Foulon, Guillaume
    De Cremoux, Hubert
    Vieira, Thibault
    Antoine, Martine
    Wislez, Marie
    EUROPEAN JOURNAL OF CANCER, 2014, 50 (07) : 1239 - 1246
  • [46] Effectiveness of ALK inhibitors in treatment of CNS metastases in NSCLC patients
    Gil, Michal
    Knetki-Wroblewska, Magdalena
    Nizinski, Przemyslaw
    Strzemski, Maciej
    Krawczyk, Pawel
    ANNALS OF MEDICINE, 2023, 55 (01) : 1018 - 1028
  • [47] Lorlatinib Tolerability and Association With Clinical Outcomes in Patients With Advanced ALK- or ROS1-Rearranged NSCLC: A Brief Report
    Thummalapalli, Rohit
    Choudhury, Noura J.
    Ehrich, Fiona
    Beardslee, Tyler
    Brazel, Danielle
    Zhang, Shannon S.
    Merchant, Shelby
    Chen, Monica F.
    Heller, Glenn
    Ramalingam, Suresh S.
    Ou, Sai-Hong Ignatius
    Mileham, Kathryn F.
    Riely, Gregory J.
    JTO CLINICAL AND RESEARCH REPORTS, 2023, 4 (08):
  • [48] Prolonging TKI treatment after limited progression with local therapy in ALK- or EGFR-NSCLC
    Laursen, Michael R. T.
    Nielsen, Anna M.
    Jensen, Rawia F. G.
    Andersen, Jon L.
    Persson, Gitte F.
    RADIOTHERAPY AND ONCOLOGY, 2024, 194 : S1749 - S1753
  • [49] Efficacy of ALK inhibitors on NSCLC brain metastases: A systematic review and pooled analysis of 21 studies
    Petrelli, Fausto
    Lazzari, Chiara
    Ardito, Raffaele
    Borgonovo, Karen
    Bulotta, Alessandra
    Conti, Barbara
    Cabiddu, Mary
    Capitanio, Jody Filippo
    Brighenti, Matteo
    Ghilardi, Mara
    Gianni, Luca
    Barni, Sandro
    Gregorc, Vanesa
    PLOS ONE, 2018, 13 (07):
  • [50] EMMPRIN (CD147) is induced by C/EBPβ and is differentially expressed in ALK plus and ALK- anaplastic large-cell lymphoma
    Schmidt, Janine
    Bonzheim, Irina
    Steinhilber, Julia
    Montes-Mojarro, Ivonne A.
    Ortiz-Hidalgo, Carlos
    Klapper, Wolfram
    Fend, Falko
    Quintanilla-Martinez, Leticia
    LABORATORY INVESTIGATION, 2017, 97 (09) : 1095 - 1102