Cancer Treatment-Related Complications in Patients With Hypertrophic Cardiomyopathy

被引:2
|
作者
Zampieri, Mattia [1 ,8 ]
Schoonvelde, Stephan A. C. [2 ]
Vinci, Michele
Meattini, Icro [1 ,4 ,5 ]
Visani, Luca [4 ]
Fornaro, Alessandra
Coppini, Raffaele [6 ]
Romei, Andrea [4 ,5 ]
Marchi, Alberto
Morelli, Ilaria [4 ,5 ]
van Slegtenhorst, Marion A. [3 ]
Palinkas, Eszter Dalma [7 ]
Livi, Lorenzo [4 ,5 ]
Michels, Michelle [2 ]
Olivotto, Iacopo [6 ]
机构
[1] Univ Hosp IRCCS, Florence, Italy
[2] Cardiovasc Inst, Thorax Ctr, Dept Cardiol, Erasmus MC, Rotterdam, Netherlands
[3] Erasmus MC Univ Med Ctr Rotterdam, Dept Clin Genet, Rotterdam, Netherlands
[4] Oncol Dept, Radiat Oncol Unit, Azienda Osped Univ Careggi, Florence, Italy
[5] Univ Florence, Dept Expt & Clin Biomed Sci M Serio, Florence, Italy
[6] Careggi Univ Hosp, Dept Expt & Clin Med, Florence, Italy
[7] Univ Szeged, Doctoral Sch Clin Med, Szeged, Hungary
[8] Viale Gaetano Pieraccini 24, I-50139 Florence, Italy
关键词
EUROPEAN ASSOCIATION; AMERICAN SOCIETY; CARDIOVASCULAR COMPLICATIONS; CARDIAC-HYPERTROPHY; EXPERT CONSENSUS; DIAGNOSIS; ESC; ECHOCARDIOGRAPHY; CARDIOPROTECTION; CARDIOTOXICITY;
D O I
10.1016/j.mayocp.2023.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To describe the potential clinical cardiotoxicity of oncological treatments in a cohort of consecutive patients with hypertrophic cardiomyopathy (HCM), systematically followed -up at two national referral centers for HCM. Cardiotoxicity relates to the direct effects of cancer -related treatment on heart function, commonly presenting as left ventricular contractile dysfunction. However, limited data are available regarding cardiotoxic effects on HCM as most studies have not specifically analyzed the effects of oncological treatment in HCM populations. This gap in knowledge may lead to unjustified restriction of HCM patients from receiving curative cancer treatments. Methods: We retrospectively analyzed clinical and instrumental data of all consecutive HCM patients who underwent oncological treatment between January 2000 and December 2020 collected in a centralized database. Results: Of 3256 HCM patients, 121 (3.7%) had cancer; 110 (90.9%) underwent oncological surgery, 45 (37.2%) received chemotherapy, and 22 (18.2%) received chest radiation therapy (cRT). After a median follow-up of 5.2 years (Q1 -Q3: 2-13 years) from oncological diagnosis, 32 patients died. The cumulative survival at 5 years was 79.9%. The cause of death was mainly attributed to the oncological condition, whereas four patients died of sudden cardiac death without receiving previous chemotherapy or cRT. No patient interrupted or reduced the dose of oncological treatment due to cardiac dysfunction. No sustained ventricular tachyarrhythmia was induced by chemotherapy or radiation therapy. Conclusion: Cancer treatment was well tolerated in HCM patients. In our consecutive series, none died of cardiovascular complications induced by chemotherapy or cRT and they did not require interruption or substantial treatment tapering due to cardiovascular toxic effects. Although a multidisciplinary evaluation is necessary and regimens must be tailored individually, the diagnosis of HCM per se should not be considered a contraindication to receive optimal curative cancer treatment.
引用
收藏
页码:218 / 228
页数:11
相关论文
共 50 条
  • [41] Effect of Mavacamten on Echocardiographic Features in Symptomatic Patients With Obstructive Hypertrophic Cardiomyopathy
    Hegde, Sheila M.
    Lester, Steven J.
    Solomon, Scott D.
    Michels, Michelle
    Elliott, Perry M.
    Nagueh, Sherif F.
    Choudhury, Lubna
    Zemanek, David
    Zwas, Donna R.
    Jacoby, Daniel
    Wang, Andrew
    Ho, Carolyn Y.
    Li, Wanying
    Sehnert, Amy J.
    Olivotto, Iacopo
    Abraham, Theodore P.
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2021, 78 (25) : 2518 - 2532
  • [42] Heart failure risk assessment in patients with hypertrophic cardiomyopathy based on the H2FPEF score
    Laenens, Dorien
    Zegkos, Thomas
    Kamperidis, Vasileios
    Wong, Raymond C. C.
    Li, Tony Yi-Wei
    Sia, Ching-Hui
    Kong, William K. F.
    Efthimiadis, Georgios
    Poh, Kian Keong
    Ziakas, Antonios
    Bax, Jeroen J.
    Marsan, Nina Ajmone
    EUROPEAN JOURNAL OF HEART FAILURE, 2024, 26 (10) : 2173 - 2182
  • [43] Markers of responsiveness to disopyramide in patients with hypertrophic cardiomyopathy
    Habib, Manhal
    Hoss, Sara
    Bruchal-Garbicz, Beata
    Chan, Raymond H.
    Rakowski, Harry
    Williams, Lynne
    Adler, Arnon
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2019, 297 : 75 - 82
  • [44] Left-ventricular outflow tract acceleration time is associated with symptoms in patients with obstructive hypertrophic cardiomyopathy
    Huurman, Roy
    Michels, Michelle
    Bowen, Daniel J.
    van Slegtenhorst, Marjon A.
    Hirsch, Alexander
    Schinkel, Arend F. L.
    JOURNAL OF ULTRASOUND, 2021, 24 (03) : 279 - 287
  • [45] Prevalence and Clinical Correlates of Right Ventricular Dysfunction in Patients With Hypertrophic Cardiomyopathy
    Finocchiaro, Gherardo
    Knowles, Joshua W.
    Pavlovic, Aleksandra
    Perez, Marco
    Magavern, Emma
    Sinagra, Gianfranco
    Haddad, Francois
    Ashley, Euan A.
    AMERICAN JOURNAL OF CARDIOLOGY, 2014, 113 (02) : 361 - 367
  • [46] Distinct Phenotypic Groups and Related Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy
    Kwak, Soongu
    Kim, Jihoon
    Park, Chan-Soon
    Lee, Hyun-Jung
    Park, Jun-Bean
    Lee, Seung-Pyo
    Kim, Yong-Jin
    Kim, Hyung-Kwan
    Lee, Sang-Chol
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2024, 13 (20):
  • [47] Association of Multiple Nonhypertrophic Cardiomyopathy-Related Genetic Variants and Outcomes in Patients With Hypertrophic Cardiomyopathy
    Hiruma, Takashi
    Inoue, Shunsuke
    Dai, Zhehao
    Nomura, Seitaro
    Kubo, Toru
    Sugiura, Kenta
    Suzuki, Atsushi
    Kashimura, Takeshi
    Matsushima, Shouji
    Yamada, Takanobu
    Tobita, Takashige
    Katoh, Manami
    Ko, Toshiyuki
    Ito, Masamichi
    Ishida, Junichi
    Amiya, Eisuke
    Hatano, Masaru
    Takeda, Norifumi
    Takimoto, Eiki
    Akazawa, Hiroshi
    Morita, Hiroyuki
    Yamaguchi, Junichi
    Inomata, Takayuki
    Tsutsui, Hiroyuki
    Kitaoka, Hiroaki
    Aburatani, Hiroyuki
    Takeda, Norihiko
    Komuro, Issei
    JACC-HEART FAILURE, 2024, 12 (12) : 2041 - 2052
  • [48] Tenosynovial complications identify TTR cardiac amyloidosis among patients with hypertrophic cardiomyopathy phenotype
    Cappelli, F.
    Zampieri, M.
    Fumagalli, C.
    Nardi, G.
    Del Monaco, G.
    Cerinic, M. Matucci
    Allinovi, M.
    Taborchi, G.
    Martone, R.
    Gabriele, M.
    Ungar, A.
    Pignone, A. Moggi
    Marchionni, N.
    Di Mario, C.
    Olivotto, I
    Perfetto, F.
    JOURNAL OF INTERNAL MEDICINE, 2021, 289 (06) : 831 - 839
  • [49] Cardiooncology-dealing with modern drug treatment, long-term complications, and cancer survivorship
    de Wall, Claudia
    Bauersachs, Johann
    Berliner, Dominik
    CLINICAL & EXPERIMENTAL METASTASIS, 2021, 38 (04) : 361 - 371
  • [50] Strain echocardiography is related to fibrosis and ventricular arrhythmias in hypertrophic cardiomyopathy
    Haland, Trine F.
    Almaas, Vibeke M.
    Hasselberg, Nina E.
    Saberniak, Jorg
    Leren, Ida S.
    Hopp, Einar
    Edvardsen, Thor
    Haugaa, Kristina H.
    EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING, 2016, 17 (06) : 613 - 621