Adjuvant Treatment with 5-Fluorouracil and Oxaliplatin Does Not Influence Cardiac Function, Neurovascular Control, and Physical Capacity in Patients with Colon Cancer.
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Chemotherapy, Adjuvant
Colonic Neoplasms
/ drug therapy
Fluorouracil
/ therapeutic use
Humans
Leucovorin
/ therapeutic use
Neoplasm Recurrence, Local
/ pathology
Neoplasm Staging
Organoplatinum Compounds
/ therapeutic use
Oxaliplatin
/ therapeutic use
Stroke Volume
Ventricular Function, Left
Adjuvant chemotherapy
Cardiac function
Colon cancer
Functional capacity
Peripheral vascular function
Sympathetic nerve activity
Journal
The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
19
03
2020
accepted:
21
07
2020
pubmed:
8
8
2020
medline:
22
6
2021
entrez:
8
8
2020
Statut:
ppublish
Résumé
Adjuvant chemotherapy with 5-fluorouracil (5-FU) and oxaliplatin increases recurrence-free and overall survival in patients with colon adenocarcinoma. It is known that these drugs have been associated with cardio- and neurotoxicity. We investigated the effects of 5-FU ± oxaliplatin on cardiac function, vascular responses, neurovascular control, and physical capacity in patients with colon cancer. Twenty-nine patients with prior colectomy for stage II-III adenocarcinoma and clinical indication for adjuvant chemotherapy were allocated to receive 5-FU (n = 12) or 5-FU + oxaliplatin (n = 17), according to the oncologist's decision. All the analyses were performed just before and after the end of chemotherapy. Cardiac function was assessed by echocardiography and speckle tracking, and cardiac autonomic control was assessed by heart rate variability (HRV). Vascular endothelial function was assessed by flow-mediated dilation (FMD). Muscle sympathetic nerve activity (MSNA) was directly recorded by microneurography technique, and muscle blood flow by venous occlusion plethysmography. Physical capacity was evaluated by cardiopulmonary exercise test. Chemotherapy (pooled data) did not significantly change left ventricular ejection fraction (58 ± 1 vs. 55 ± 2%, p = .14), longitudinal strain (-18 ± 1 vs. -18 ± 1%, p = .66), and HRV. Likewise, chemotherapy did not significantly change FMD, muscle blood flow, and MSNA (33 ± 2 vs. 32 ± 1 bursts/min, p = .31). Physical capacity was not significantly changed in both groups. Similar findings were observed when the patients were subdivided in 5-FU and 5-FU + oxaliplatin treatment groups. 5-FU and 5-FU + oxaliplatin did not significantly change cardiac function, HRV, vascular responses, MSNA, and physical capacity. This study provides evidence that adjuvant treatment with 5-FU ± oxaliplatin is well tolerated and does not promote changes compatible with long-term cardiotoxicity. Adjuvant chemotherapy with 5-fluorouracil (5-FU) and oxaliplatin increases recurrence-free and overall survival in patients with colon adenocarcinoma; however, these drugs have been associated with cardio- and neurotoxicity. This study investigated the effects of these drugs on cardiac function, vascular responses, neurovascular control, and physical capacity in patients with colon cancer. It was found that 5-FU and oxaliplatin did not significantly change cardiac function, cardiac autonomic control, vascular endothelial function, muscle sympathetic nerve activity, and physical capacity. This study provides evidence that adjuvant treatment with 5-FU ± oxaliplatin is well tolerated and does not promote changes compatible with long-term cardiotoxicity.
Sections du résumé
BACKGROUND
Adjuvant chemotherapy with 5-fluorouracil (5-FU) and oxaliplatin increases recurrence-free and overall survival in patients with colon adenocarcinoma. It is known that these drugs have been associated with cardio- and neurotoxicity. We investigated the effects of 5-FU ± oxaliplatin on cardiac function, vascular responses, neurovascular control, and physical capacity in patients with colon cancer.
METHODS
Twenty-nine patients with prior colectomy for stage II-III adenocarcinoma and clinical indication for adjuvant chemotherapy were allocated to receive 5-FU (n = 12) or 5-FU + oxaliplatin (n = 17), according to the oncologist's decision. All the analyses were performed just before and after the end of chemotherapy. Cardiac function was assessed by echocardiography and speckle tracking, and cardiac autonomic control was assessed by heart rate variability (HRV). Vascular endothelial function was assessed by flow-mediated dilation (FMD). Muscle sympathetic nerve activity (MSNA) was directly recorded by microneurography technique, and muscle blood flow by venous occlusion plethysmography. Physical capacity was evaluated by cardiopulmonary exercise test.
RESULTS
Chemotherapy (pooled data) did not significantly change left ventricular ejection fraction (58 ± 1 vs. 55 ± 2%, p = .14), longitudinal strain (-18 ± 1 vs. -18 ± 1%, p = .66), and HRV. Likewise, chemotherapy did not significantly change FMD, muscle blood flow, and MSNA (33 ± 2 vs. 32 ± 1 bursts/min, p = .31). Physical capacity was not significantly changed in both groups. Similar findings were observed when the patients were subdivided in 5-FU and 5-FU + oxaliplatin treatment groups. 5-FU and 5-FU + oxaliplatin did not significantly change cardiac function, HRV, vascular responses, MSNA, and physical capacity.
CONCLUSION
This study provides evidence that adjuvant treatment with 5-FU ± oxaliplatin is well tolerated and does not promote changes compatible with long-term cardiotoxicity.
IMPLICATIONS FOR PRACTICE
Adjuvant chemotherapy with 5-fluorouracil (5-FU) and oxaliplatin increases recurrence-free and overall survival in patients with colon adenocarcinoma; however, these drugs have been associated with cardio- and neurotoxicity. This study investigated the effects of these drugs on cardiac function, vascular responses, neurovascular control, and physical capacity in patients with colon cancer. It was found that 5-FU and oxaliplatin did not significantly change cardiac function, cardiac autonomic control, vascular endothelial function, muscle sympathetic nerve activity, and physical capacity. This study provides evidence that adjuvant treatment with 5-FU ± oxaliplatin is well tolerated and does not promote changes compatible with long-term cardiotoxicity.
Identifiants
pubmed: 32762143
doi: 10.1634/theoncologist.2020-0225
pmc: PMC8108063
doi:
Substances chimiques
Organoplatinum Compounds
0
Oxaliplatin
04ZR38536J
Leucovorin
Q573I9DVLP
Fluorouracil
U3P01618RT
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1956-e1967Commentaires et corrections
Type : ErratumIn
Informations de copyright
© 2020 AlphaMed Press.
Références
Circulation. 2003 Feb 4;107(4):565-70
pubmed: 12566367
Nature. 2015 May 14;521(7551):S1
pubmed: 25970450
Am J Physiol Heart Circ Physiol. 2011 Jan;300(1):H2-12
pubmed: 20952670
Ther Adv Med Oncol. 2018 Jun 18;10:1758835918780140
pubmed: 29977352
Ann R Coll Surg Engl. 2016 Jul;98(6):396-400
pubmed: 27138851
Int J Cardiol. 2009 Jul 10;135(3):302-7
pubmed: 18582965
Am J Physiol Heart Circ Physiol. 2019 Jul 1;317(7):H1-H12
pubmed: 31002284
Tumori. 1982 Dec 31;68(6):505-10
pubmed: 7168016
CA Cancer J Clin. 2017 May 6;67(3):177-193
pubmed: 28248415
J Clin Oncol. 2007 Jun 1;25(16):2198-204
pubmed: 17470851
Eur J Prev Cardiol. 2016 Oct;23(15):1599-608
pubmed: 27271264
J Hypertens. 2013 Feb;31(2):287-91
pubmed: 23169234
J Clin Oncol. 2007 Aug 20;25(24):3732-8
pubmed: 17704423
Med Oncol. 2010 Jun;27(2):416-20
pubmed: 19415535
J Clin Oncol. 1997 Feb;15(2):808-15
pubmed: 9053508
Neurosci Lett. 2015 Jun 2;596:90-107
pubmed: 25459280
Br J Surg. 2016 May;103(6):744-752
pubmed: 26914526
Ann Oncol. 2014 May;25(5):1059-64
pubmed: 24558023
Mol Clin Oncol. 2013 Jan;1(1):175-179
pubmed: 24649143
J Am Coll Cardiol. 2014 Jul 1;63(25 Pt A):2751-68
pubmed: 24703918
Clin Colorectal Cancer. 2012 Jun;11(2):93-100
pubmed: 22154408
Pak J Pharm Sci. 2014 Sep;27(5 Spec no):1409-18
pubmed: 25176229
Eur Heart J. 1996 Mar;17(3):354-81
pubmed: 8737210
Eur J Neurol. 2014 Dec;21(12):1471-7
pubmed: 25041285
Expert Opin Drug Saf. 2009 Mar;8(2):191-202
pubmed: 19309247
J Clin Oncol. 2015 Dec 10;33(35):4176-87
pubmed: 26527776
Cancer. 1993 Oct 1;72(7):2242-7
pubmed: 8374883
Eur J Heart Fail. 2010 Jan;12(1):58-65
pubmed: 20023046
Jpn J Clin Oncol. 2004 May;34(5):262-8
pubmed: 15231861
J Am Coll Cardiol. 2003 Sep 3;42(5):854-60
pubmed: 12957432
Lancet. 2007 Dec 15;370(9604):2020-9
pubmed: 18083404
Pharmacotherapy. 1997 Jul-Aug;17(4):729-36
pubmed: 9250550
N Engl J Med. 2004 Jun 3;350(23):2343-51
pubmed: 15175436
J Clin Oncol. 2009 Jul 1;27(19):3109-16
pubmed: 19451431
J Cancer Res Ther. 2007 Jul-Sep;3(3):169-71
pubmed: 18079582
Oncol Rep. 2000 Jul-Aug;7(4):887-90
pubmed: 10854564
Asia Pac J Clin Oncol. 2017 Dec;13(6):345-355
pubmed: 28653815
Ann Oncol. 1997 Jul;8(7):705-8
pubmed: 9296228
J Clin Oncol. 2010 Dec 20;28(36):5280-6
pubmed: 21079148
J Am Soc Echocardiogr. 2015 Jan;28(1):1-39.e14
pubmed: 25559473
Ann Pharmacother. 1994 Mar;28(3):374-8
pubmed: 8193429
CA Cancer J Clin. 2018 Nov;68(6):394-424
pubmed: 30207593
Cardiol J. 2012;19(5):453-8
pubmed: 23042307
Radiother Oncol. 1988 Sep;13(1):41-6
pubmed: 3187073
Cancer Chemother Pharmacol. 2012 Jan;69(1):57-64
pubmed: 21603868