

Features of clinical manifestations of ischemic stroke in cancer
https://doi.org/10.30629/2658-7947-2025-30-3-13-22
Abstract
Determination of clinical characteristics of ischemic stroke (IS) in cancer patients is difficult due to the involvement of both traditional and cancer-associated mechanisms in stroke pathogenesis. To date, there are no clear diagnostic criteria for cancer-associated stroke, which is often one of the first clinical manifestations of the oncological process.
The aim of the study — to research the clinical manifestations of ischemic stroke associated with cancer.
Material and methods. A comparative analysis of 84 cases of IS with concomitant cancer (main group) and 239 cases of IS without cancer (comparison group) was performed. All patients were assessed for the severity of IS according to the NIHSS scale, stroke subtype according to TOAST, disease outcome, localization and size of the cerebral infarction territory according to neuroimaging data; presence of hemorrhagic transformation. The parameters of coagulation hemostasis (international normalized ratio (INR), activated partial thromboplastin time (APTT), prothrombin index (PTI), fibrinogen, platelet count) were assessed at the time of admission to the hospital. The follow-up of patients in the main group was studied based on the data from outpatient cards in the RTMIS system, using a telephone survey of patients and their relatives 3 months and 1 year after the stroke.
Results. During the observation period, 2027 patients with ischemic stroke were hospitalized, of which 84 patients (the main group) were diagnosed with active stage cancer (4.14%). In the main group, 20 patients (23.8%) were diagnosed with cancer during hospitalization at the Regional Vascular Center due to ischemic stroke. The most common localization in the study group was colon cancer (19.04%). Lung cancer was diagnosed in 13.1%, bladder cancer — in 10.7%. According to the histological type, adenocarcinomas were most often detected — in 35 cases (41.6%). The median age in the main group was 69 years [65;75], in the comparison group — 65 years [58;72] (p < 0.001). In the main group of diseases, large-artery atherosclerosis (14.3% vs. 43.1%, respectively, p < 0.001) and cardioembolic stroke subtypes (14.3% vs. 30.5%, respectively, p = 0.004) were diagnosed less frequently. In the main group, there was a more frequent diagnosis of the IS subtype of other determined etiology (13.1% vs. 3.8%, respectively; p = 0.003) and of undetermined etiology according to TOAST (47.6% vs. 8.8%, respectively; p < 0.001). In the main group, in patients, compared with the consequence without cancer, multifocal infarctions that developed simultaneously in both carotid basins were more often diagnosed (9.5% vs. 2.5%, respectively, p = 0.011; OR = 4.09, 95% CI: 1.37–12.15). Upon admission to the hospital, the PTI values were higher in the main group of patients compared to patients without cancer (102.5 [84.0; 111.0] versus 87.7 [72.4; 99.0], p = 0.003). In patients with ischemic stroke, who were diagnosed with cancer in the RVC, higher fibrinogen and platelet levels were noted (p = 0.022 and p = 0.008). Mortality within 3 months after the suffered ischemic stroke in the group was 21.4% (18 patients), within a year — 42.9% (36 patients).
Conclusion. Cancer-associated coagulopathy probably plays a leading role in the development of ischemic stroke in cancer.
About the Authors
L. V. AmmosovaRussian Federation
Yakutsk
S. A. Chugunova
Russian Federation
Yakutsk
S. K. Krivykh
Russian Federation
Yakutsk
References
1. Dardiotis E, Aloizou AM, Markoula S, Siokas V, Tsarouhas K, Tzanakakis G, Libra M, Kyritsis AP, Brotis AG, Aschner M, Gozes I, Bogdanos DP, Spandidos DA, Mitsias PD, Tsatsakis A. Cancer-associated stroke: Pathophysiology, detection and management (Review). Int J Oncol. 2019;54(3):779–796. https://doi.org/10.3892/ijo.2019.4669
2. Bang OY, Chung JW, Lee MJ, Seo WK, Kim GM, Ahn MJ. Cancer-Related Stroke: An Emerging Subtype of Ischemic Stroke with Unique Pathomechanisms. J Stroke. 2020;22(1):1–10. https://doi.org/10.5853/jos.2019.02278
3. Graus F, Rogers LR, Posner JB. Cerebrovascular complications in patients with cancer. Medicine (Baltimore). 1985;64(1):16–35. https://doi.org/10.1097/00005792-198501000-00002
4. Varki A. Trousseau’s syndrome: multiple defi nitions and multiple mechanisms. Blood. 2007;110(6):1723–9. https://doi.org/10.1182/blood-2006-10-053736
5. Navi BB, Reiner AS, Kamel H, Iadecola C, Okin PM, Tagawa ST, Panageas KS, DeAngelis LM. Arterial thromboem-bolic events preceding the diagnosis of cancer in older persons. Blood. 2019;133(8):781–789. https://doi.org/10.1182/blood-2018-06-860874
6. Taccone FS, Jeangette SM, Blecic SA. First-ever stroke as initial presentation of systemic cancer. J Stroke Cerebrovasc Dis. 2008;17(4):169–74. https://doi.org/10.1016/j.jstrokecerebrovasdis.2008.01.007
7. Lee KP, Huang HC, Tsai JY, Hsu LC. Eff ects of cancer on stroke recurrence and mortality: A single-center retrospective cohort study. eNeurologicalSci. 2023;32:100474. https://doi.org/10.1016/j.ensci.2023.100474
8. Kim H, Kim JT, Lee JS, Kim BJ, Kang J, Lee KJ, Park JM, Kang K, Lee SJ, Kim JG, Cha JK, Kim DH, Park TH, Lee KB, Lee J, Hong KS, Cho YJ, Park HK, Lee BC, Yu KH, Oh MS, Kim DE, Ryu WS, Choi JC, Kwon JH, Kim WJ, Shin DI, Yum KS, Sohn SI, Hong JH, Lee SH, Park MS, Choi KH, Lee J, Bae HJ. Stroke of Other Determined Etiology: Results From the Nationwide Multicenter Stroke Registry. Stroke. 2022;53(8):2597-2606. https://doi.org/10.1161/strokeaha.121.037582
9. Bao L, Zhang S, Gong X, Cui G. Trousseau Syndrome Related Cerebral Infarction: Clinical Manifestations, Laboratory Findings and Radiological Features. J Stroke Cerebrovasc Dis. 2020;29(9):104891. https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.104891
10. Nouh AM, Staff I, Finelli PF. Three Territory Sign: An MRI marker of malignancy-related ischemic stroke (Trousseau syndrome). Neurol Clin Pract. 2019;9(2):124–128. https://doi.org/10.1212/cpj.0000000000000603
11. Ling Y, Li Y, Zhang X, Dong L, Wang J. Clinical features of Trousseau’s syndrome with multiple acute ischemic strokes. Neurol Sci. 2022;43(4):2405–2411. https://doi.org/10.1007/s10072-021-05619-y
12. Guo L, Wang L, Liu W. Ability of the number of territories involved on DWI-MRI to predict occult systemic malignancy in cryptogenic stroke patients. J Stroke Cerebrovasc Dis. 2020;29(7):104823. https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.104823
13. Tsushima M, Metoki N, Hagii J, Saito S, Shiroto H, Yasujima M, Kato T, Kudo N, Toyama Y, Yokono Y, Nozaka M, Kawamura Y, Nakata M, Tomita H. D-dimer and C-reactive Protein as Potential Biomarkers for Diagnosis of Trousseau’s Syndrome in Patients with Cerebral Embolism. J Stroke Cerebrovasc Dis. 2020;29(2):104534. https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.104534
14. Finelli PF, Nouh A. Three-Territory DWI Acute Infarcts: Diagnostic Value in Cancer-Associated Hypercoagulation Stroke (Trousseau Syndrome). AJNR Am J Neuroradiol. 2016;37(11):2033-2036. https://doi.org/10.3174/ajnr.a4846
15. Wang JY, Zhang GJ, Zhuo SX, Wang K, Hu XP, Zhang H, Qu LD. D-dimer > 2.785 μg/ml and multiple infarcts ≥ 3 vascular territories are two characteristics of identifying cancer-associated ischemic stroke patients. Neurol Res. 2018;40(11):948–954. https://doi.org/10.1080/01616412.2018.1504179
16. Liu M, Ellis D, Duncan A, Belagaje S, Belair T, Henriquez L, Rangaraju S, Nahab F. The Utility of the Markers of Coagulation and Hemostatic Activation Profi le in the Management of Embolic Strokes of Undetermined Source. J Stroke Cerebrovasc Dis. 2021;30(3):105592. https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.105592
17. Ellis D, Rangaraju S, Duncan A, Hoskins M, Raza SA, Rahman H, Winningham M, Belagaje S, Bianchi N, Mohamed GA, Obideen M, Sharashidze V, Belair T, Henriquez L, Nahab F. Coagulation markers and echocardiography predict atrial fibrillation, malignancy or recurrent stroke after cryptogenic stroke. Medicine (Baltimore). 2018;97(51):e13830. https://doi.org/10.1097/md.0000000000013830
18. Nahab F, Sharashidze V, Liu M, Rathakrishnan P, El Jamal S, Duncan A, Hoskins M, Marmarchi F, Belagaje S, Bianchi N, Belair T, Henriquez L, Monah K, Rangaraju S. Markers of coagulation and hemostatic activation aid in identifying causes of cryptogenic stroke. Neurology. 2020;94(18):e1892-e1899. https://doi.org/10.1212/wnl.0000000000009365
19. Salazar-Camelo RA, Moreno-Vargas EA, Cardona AF, Bayona-Ortiz HF. Ischemic stroke: A paradoxical manifestation of cancer. Crit Rev Oncol Hematol.2021;157:103181. https://doi.org/10.1016/j.critrevonc.2020.103181
20. Costamagna G, Navi BB, Beyeler M, Hottinger AF, Alberio L, Michel P. Ischemic Stroke in Cancer: Mechanisms, Biomarkers, and Implications for Treatment. Semin Thromb Hemost. 2024;50(3):342–359. https://doi.org/10.1055/s-0043-1771270
21. Chi X, Zhao R, Pei H, Xing A, Hu S, Chen J, Mao Y, Zheng X. Diff usion-weighted imaging-documented bilateral small embolic stroke involving multiple vascular territories may indicate occult cancer: A retrospective case series and a brief review of the literature. Aging Med (Milton). 2020;3(1):53–59. https://doi.org/10.1002/agm2.12105
22. Grazioli S, Paciaroni M, Agnelli G, Acciarresi M, Alberti A, D’Amore C, Caso V, Venti M, Guasti L, Ageno W, Squizzato A. Cancer-associated ischemic stroke: A retrospective multicentre cohort study. Thromb Res. 2018;165:33–37. https://doi.org/10.1016/j.thromres.2018.03.011
23. Nezu T, Hosomi N, Aoki S, Naito H, Torii T, Kurashige T, Sugiura T, Kuzume D, Morimoto Y, Yoshida T, Yagita Y, Oyama N, Eto F, Shiga Y, Kinoshita N, Kamimura T, Ueno H, Ohshita T, Maruyama H. Short-term or long-term outcomes for stroke patients with cancer according to biological markers. J Neurol Sci. 2022;436:120246. https://doi.org/10.1016/j.jns.2022.120246
24. Göcmen J, Steinauer F, Kielkopf M, Branca M, Kurmann CC, Mujanovic A, Clénin L, Silimon N, Boronylo A, Scutelnic A, Meinel T, Kaesmacher J, Bücke P, Seiff ge D, Costamagna G, Michel P, Fischer U, Arnold M, Navi BB, Pabst T, Berger MD, Jung S, Beyeler M. Mortality in acute ischemic stroke patients with new cancer diagnosed during the index hospitalization versus after discharge. J Stroke Cerebrovasc Dis. 2024;33(10):107899. https://doi.org/10.1016/j.jstrokecerebrovasdis.2024.107899
25. Lee MJ, Chung JW, Ahn MJ, Kim S, Seok JM, Jang HM, Kim GM, Chung CS, Lee KH, Bang OY. Hypercoagulability and Mortality of Patients with Stroke and Active Cancer: The OASIS-CANCER Study. J Stroke. 2017;19(1):77–87. https://doi.org/10.5853/jos.2016.00570
Review
For citations:
Ammosova L.V., Chugunova S.A., Krivykh S.K. Features of clinical manifestations of ischemic stroke in cancer. Russian neurological journal. 2025;30(3):13-22. (In Russ.) https://doi.org/10.30629/2658-7947-2025-30-3-13-22