Literature DB >> 3513941

Cardiac complications after bone marrow transplantation. A report on a series of 63 consecutive transplantations.

B Cazin, N C Gorin, J P Laporte, B Gallet, L Douay, M Lopez, A Najman, G Duhamel.   

Abstract

Cardiac complications related to bone marrow grafting were investigated in a group of 63 patients undergoing bone marrow transplantation (57 autologous, 6 allogeneic) in the transplant unit of Hôpital Saint-Antoine (Paris, France) between February 1977 and October 1983. The pregraft regimen was cyclophosphamide, 6-thioguanine, cytosine arabinoside, and CCNU (TACC) in 39 cases, cyclophosphamide (CY) associated with whole-body irradiation in 16 cases, and multiple chemotherapeutic agents in 8 cases. The study was retrospective in 49 patients, and prospective in 14. The morbidity was 43% and the mortality 9%. There were 6 fatal cases of cardiomyopathies and/or pericarditis, 14 nonfatal cases of heart failure, 7 nonfatal cases of pure pericarditis, and 32 arythmias including 14 bradycardias, diversely associated on a total of 27 patients. Cyclophosphamide and/or TACC/cyclophosphamide, 6-thioguanine, cytosine arabinoside, and BCNU (BACT) were the factors basically responsible for the cardiac toxicity. The best-defined entity was an acute fatal cardiomyopathy with associated pericarditis of which we report three additional cases. The best predictors of CY toxicity were the daily weight (a gain of more than 2 kg for more than 48 hours) and the electrocardiogram (a decrease of more than 14% in the sum of the QRS complexes in the standard leads on the fourth day of chemotherapy). Routine echocardiography confirmed the high incidence of subclinical cardiac abnormalities and their reversibility. It would seem that radiotherapy and anthracyclines play a secondary role. Currently, we consider that cardiac toxicity is one of the most important limiting factors for bone marrow transplantation. We suggest, therefore, that the transplantation should be done as early as possible and preference should be given whenever possible to whole-body irradiation over high-dose chemotherapy combinations such as TACC.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3513941     DOI: 10.1002/1097-0142(19860515)57:10<2061::aid-cncr2820571031>3.0.co;2-h

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  27 in total

Review 1.  Cyclophosphamide toxicity. Characterising and avoiding the problem.

Authors:  L H Fraiser; S Kanekal; J P Kehrer
Journal:  Drugs       Date:  1991-11       Impact factor: 9.546

Review 2.  Optimisation of cyclophosphamide therapy in systemic vasculitis.

Authors:  R Richmond; T W McMillan; R A Luqmani
Journal:  Clin Pharmacokinet       Date:  1998-01       Impact factor: 6.447

Review 3.  Advanced heart failure due to cancer therapy.

Authors:  Sachin Shah; Anju Nohria
Journal:  Curr Cardiol Rep       Date:  2015       Impact factor: 2.931

4.  Cardiac damage in autologous bone marrow transplant patients: an autopsy study. Cardiotoxic pretreatment as a major risk factor.

Authors:  A von Herbay; B Dörken; G Mall; M Körbling
Journal:  Klin Wochenschr       Date:  1988-12-01

5.  Severe delayed heart failure in three multiple sclerosis patients previously treated with mitoxantrone.

Authors:  Sophie Goffette; Vincent van Pesch; Jean Louis Vanoverschelde; Emmanuel Morandini; Christian J M Sindic
Journal:  J Neurol       Date:  2005-04-18       Impact factor: 4.849

6.  Transient, high-grade atrioventricular block from high-dose cyclophosphamide.

Authors:  Nayan Agarwal; Thomas A Burkart
Journal:  Tex Heart Inst J       Date:  2013

Review 7.  Cardiotoxicity of chemotherapeutic agents: incidence, treatment and prevention.

Authors:  V B Pai; M C Nahata
Journal:  Drug Saf       Date:  2000-04       Impact factor: 5.606

Review 8.  Cyclophosphamide and cancer: golden anniversary.

Authors:  Ashkan Emadi; Richard J Jones; Robert A Brodsky
Journal:  Nat Rev Clin Oncol       Date:  2009-09-29       Impact factor: 66.675

9.  Fludarabine-based nonmyeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics.

Authors:  Mitchell E Horwitz; Ivan Spasojevic; Ashley Morris; Marilyn Telen; James Essell; Cristina Gasparetto; Keith Sullivan; Gwynn Long; John Chute; Nelson Chao; David Rizzieri
Journal:  Biol Blood Marrow Transplant       Date:  2007-12       Impact factor: 5.742

10.  Post-transplant bendamustine reduces GvHD while preserving GvL in experimental haploidentical bone marrow transplantation.

Authors:  Jessica Stokes; Emely A Hoffman; Yi Zeng; Nicolas Larmonier; Emmanuel Katsanis
Journal:  Br J Haematol       Date:  2016-03-31       Impact factor: 6.998

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.