18F-fluorodeoxyglucose positron emission tomography-computed tomography as a prognostic marker of imatinib-resistant gastrointestinal stromal tumors

被引:0
作者
Kawabata, Kota [1 ]
Takahashi, Tsuyoshi [1 ]
Nishida, Toshirou [2 ]
Kurokawa, Yukinori [1 ]
Yamamoto, Kazuyoshi [1 ]
Saito, Takuro [1 ]
Momose, Kota [1 ]
Yamashita, Kotaro [1 ]
Tanaka, Koji [1 ]
Makino, Tomoki [1 ]
Kawabata, Ryohei [3 ]
Takeno, Atsushi [4 ]
Nakajima, Kiyokazu [1 ]
Eguchi, Hidetoshi [1 ]
Doki, Yuichiro [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Gastroenterol Surg, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Japan Community Healthcare Org Osaka Hosp, Orthopaed Surg, 4-2-78 Fukushima,Fukushima Ku, Osaka, Japan
[3] Sakai City Med Ctr, Dept Surg, Ebarajicho, Sakai, Osaka, Japan
[4] NHO Osaka Natl Hosp, Dept Surg, 2-1-14 Hoenzaka,Chuo Ku, Osaka, Japan
关键词
Gastrointestinal stromal tumor; Imatinib resistance; Positron emission tomography-computed tomography; Maximum standardized uptake value; Surgical treatment; EARLY PREDICTION; FDG-PET/CT; MANAGEMENT; MESYLATE; TRIAL; MUTATIONS; RECURRENT; EFFICACY; CANCER; SAFETY;
D O I
10.1007/s00595-025-03029-7
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose Unresectable or metastatic GISTs often develop resistance to imatinib, but the effectiveness of other drugs is limited. Thus, surgical treatment can be considered, especially for partial resistance. FDG-PET/CT is used for the diagnosis and evaluation of GISTs. We conducted this study to establish whether FDG-PET/CT findings could guide treatment decisions and predict the prognosis of patients with imatinib-resistant GISTs. Methods We analyzed data retrospectively from 45 patients with imatinib-resistant GISTs that were assessed via FDG-PET/CT at our institution between 2003 and 2021. The patients were classified as having low (n = 18) or high (n = 27) SUVmax, with a cutoff value of 5.0. Results The overall survival (OS) of the patients with low SUVmax after the diagnosis of imatinib resistance was significantly prolonged. Multivariate analysis identified SUVmax as an independent poor prognostic factor. In 23 patients with resected imatinib-resistant lesions, a close correlation was found between the SUVmax by preoperative FDG-PET/CT and the mitotic rate. A higher SUVmax was associated with a higher mitotic rate. Patients with a low SUVmax (n = 11) had significantly longer postoperative imatinib failure-free survival than those with a high SUVmax (n = 12). Conclusions FDG-PET/CT assessment and diagnosis might reveal the pathological grades of imatinib-resistant GISTs and act as a prognostic marker.
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共 44 条
[1]   PET-based response assessment criteria for diffuse gliomas (PET RANO 1.0): a report of the RANO group [J].
Albert, Nathalie L. ;
Galldiks, Norbert ;
Ellingson, Benjamin M. ;
van den Bent, Martin J. ;
Chang, Susan M. ;
Cicone, Francesco ;
de Groot, John ;
Koh, Eng-Siew ;
Law, Ian ;
Le Rhun, Emilie ;
Mair, Maximilian J. ;
Minniti, Giuseppe ;
Ruda, Roberta ;
Scott, Andrew M. ;
Short, Susan C. ;
Smits, Marion ;
Suchorska, Bogdana ;
Tolboom, Nelleke ;
Traub-Weidinger, Tatjana ;
Tonn, Joerg-Christian ;
Verger, Antoine ;
Weller, Michael ;
Wen, Patrick Y. ;
Preusser, Matthias .
LANCET ONCOLOGY, 2024, 25 (01) :E29-E41
[2]   Clinical Effectiveness of Preoperative 18F-FDG PET/CT in Predicting Pathological Tumor Grade in Patients with Pseudomyxoma Peritonei Originating from Appendix: A Retrospective Cohort Study [J].
Aso, Kenta ;
Gohda, Yoshimasa ;
Hotta, Masatoshi ;
Minamimoto, Ryogo ;
Shimizu, Yosuke ;
Uemura, Yukari ;
Yano, Hideaki .
ANNALS OF SURGICAL ONCOLOGY, 2024, 31 (03) :1990-1995
[3]   Radiotherapy in the management of rare gastrointestinal cancers: A systematic review [J].
Bellefkih, F. Z. ;
Benchakroun, N. ;
Lalya, I. ;
Amaoui, B. ;
El Kacemi, H. ;
Acharki, A. ;
El Hfid, M. ;
El Mazghi, A. ;
Chekrine, T. ;
Bouchbika, Z. ;
Jouhadi, H. ;
Sahraoui, S. ;
Tawfiq, N. ;
Michalet, M. .
CANCER RADIOTHERAPIE, 2023, 27 (6-7) :622-637
[4]   Long-term results from a randomized phase II trial of standard- versus higher-dose imatinib mesylate for patients with unresectable or metastatic gastrointestinal stromal tumors expressing KIT [J].
Blanke, Charles D. ;
Demetri, George D. ;
von Mehren, Margaret ;
Heinrich, Michael C. ;
Eisenberg, Burton ;
Fletcher, Jonathan A. ;
Corless, Christopher L. ;
Fletcher, Christopher D. M. ;
Roberts, Peter J. ;
Heinz, Daniela ;
Wehre, Elisabeth ;
Nikolova, Zariana ;
Joensuu, Heikki .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (04) :620-625
[5]   Phase III randomized, intergroup trial assessing imatinib mesylate at two dose levels in patients with unresectable or metastatic gastrointestinal stromal tumors expressing the kit receptor tyrosine kinase: S0033 [J].
Blanke, Charles D. ;
Rankin, Cathryn ;
Demetri, George D. ;
Ryan, Christopher W. ;
von Mehren, Margaret ;
Benjamin, Robert S. ;
Raymond, A. Kevin ;
Bramwell, Vivien H. C. ;
Baker, Laurence H. ;
Maki, Robert G. ;
Tanaka, Michael ;
Hecht, J. Randolph ;
Heinrich, Michael C. ;
Fletcher, Christopher D. M. ;
Crowley, John J. ;
Borden, Ernest C. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (04) :626-632
[6]  
Blay JY, 2021, NAT REV DIS PRIMERS, V7, DOI 10.1038/s41572-021-00254-5
[7]   Impact of the KIT/PDGFRA genotype on prognosis in imatinib-naive Japanese patients with gastrointestinal stromal tumor [J].
Cho, Haruhiko ;
Nishida, Toshirou ;
Takahashi, Tsuyoshi ;
Masuzawa, Toru ;
Hirota, Seiichi .
ANNALS OF GASTROENTEROLOGICAL SURGERY, 2022, 6 (02) :241-248
[8]   Clinicopathologic Features and Molecular Characteristics of Glucose Metabolism Contributing to 18F-fluorodeoxyglucose Uptake in Gastrointestinal Stromal Tumors [J].
Cho, Min-Hee ;
Park, Cheol Keun ;
Park, Minhee ;
Kim, Won Kyu ;
Cho, Arthur ;
Kim, Hoguen .
PLOS ONE, 2015, 10 (10)
[9]   Radiopharmaceuticals for PET and SPECT Imaging: A Literature Review over the Last Decade [J].
Crisan, George ;
Moldovean-Cioroianu, Nastasia Sanda ;
Timaru, Diana-Gabriela ;
Andries, Gabriel ;
Cainap, Calin ;
Chis, Vasile .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (09)
[10]   Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors [J].
Demetri, GD ;
von Mehren, M ;
Blanke, CD ;
Van den Abbeele, AD ;
Eisenberg, B ;
Roberts, PJ ;
Heinrich, MC ;
Tuveson, DA ;
Singer, S ;
Janicek, M ;
Fletcher, JA ;
Silverman, SG ;
Silberman, SL ;
Capdeville, R ;
Kiese, B ;
Peng, B ;
Dimitrijevic, S ;
Druker, BJ ;
Corless, C ;
Fletcher, CDM ;
Joensuu, H .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (07) :472-480