Echocardiographic Myocardial Strain Analysis Describes Subclinical Cardiac Dysfunction after Craniospinal Irradiation in Pediatric and Young Adult Patients with Central Nervous System Tumors

doi:10.21203/rs.3.rs-121700/v1

Download PDF

Research

Echocardiographic Myocardial Strain Analysis Describes Subclinical Cardiac Dysfunction after Craniospinal Irradiation in Pediatric and Young Adult Patients with Central Nervous System Tumors

https://doi.org/10.21203/rs.3.rs-121700/v1

This work is licensed under a CC BY 4.0 License

Journal Publication

published 02 Feb, 2021

Read the published version in Cardio-Oncology →

You are reading this older preprint version

Read the latest preprint version →

Background: Craniospinal irradiation (CSI) is part of the treatment of central nervous system (CNS) tumors and is associated with cardiovascular disease in adults. Global myocardial strain analysis including longitudinal peak systolic strain (GLS), circumferential peak systolic strain (GCS) and radial peak systolic strain (GRS) can reveal subclinical cardiac dysfunction.

Methods: Retrospective, single-center study in patients managed with CSI vs. age-matched controls. Clinical data and echocardiography, including myocardial strain analysis, were collected at early (<12 months) and late ( 12 months) after completion of CSI.

Results: Echocardiograms were available in 20 early and 34 late patients. Patients at the late time point were older (21.7±10.4 vs. 13.3 9.6 years), and further out from CSI (13.1±8.8 vs. 0.2±0.3 years). Standard echocardiographic parameters were normal for all subjects. For the early time, CSI vs. control: GLS was -16.8 3.6% vs. -21.3 4.0% (p=0.0002), GCS was -22.5 5.2% vs. -21.3 3.4% (p=0.28), and GRS was 21.8 11.0% vs. 26.9 7.7% (p=0.07). At the late time point, CSI vs. control: GLS was -16.2 5.4% vs. -21.6 3.7% (p<0.0001), GCS was -20.9 6.8% vs. -21.9 3.5% (p=0.42), and GRS was 22.5 10.0% vs. 27.3 8.3% (p=0.03). Radiation type (proton vs. photon), and radiation dose (<30 Gy vs. 30 Gy) did not impact any parameter.

Conclusions: Subclinical cardiac systolic dysfunction by GLS is present both early and late after CSI. These results argue for inclusion of baseline cardiovascular assessment and early initiation of longitudinal follow-up post CSI.

Cardiac & Cardiovascular Systems

Oncology

craniospinal irradiation

neuro-oncology

cardiac

surveillance

Each year there are over 1.7 million new cases of cancer in the United States, including almost 16,000 pediatric patients (< 20-years-old). Advances in treatment have led to 5-year survival of > 80% for all pediatric cancer types, which amounts to more than 450,000 total survivors in the adult and pediatric age ranges.^{1, 2} Development of cardiovascular disease is the leading non-cancer cause of morbidity and mortality in this population, and radiation therapy has been reported to increase the risk of cancer related cardiotoxicity through injury of the pericardium, coronary arteries, valves, conduction system, and the myocardium.³ Few studies have looked exclusively at patients with central nervous system (CNS) cancers and exposure to craniospinal irradiation (CSI), which is known to lead to out-of-field exposure of cardiovascular tissues.^{4, 5} Surveillance guidelines for survivors of childhood cancer recommend screening for cardiotoxicity, including echocardiogram every 2–5 years based on risk factors, i.e., total cumulative anthracycline dose and/or radiation exposure.⁶ Although echocardiographic ejection fraction (EF) and shortening fraction (SF) have traditionally served to monitor left ventricular systolic function and guide clinical judgement during and after cancer-related therapies, both EF and SF are influenced by ventricular preload and afterload, and may not reflect ventricular contractility as much as they represent ventricular remodeling.⁷ Additionally, SF and EF are operator dependent and rely on geometric assumptions, with poor reproducibility reported in a large multi-center study of healthy pediatric patients.⁸ Assessment of tissue deformation by speckle tracking echocardiography may better assess left ventricular contractility with good reproducibility,⁹ and although influenced by afterload, has demonstrated the ability to detect subclinical dysfunction after cancer treatment in both pediatric and adult patients.^10–12 No prior studies have assessed temporal changes in left ventricular systolic dysfunction in patients with exposure to CSI in the setting of CNS malignancies. We postulated that exposure to CSI would lead to evidence for cardiac injury, either clinical or subclinical, and aimed to retrospectively evaluate such changes by two-dimensional speckle tracking echocardiography in a pediatric and young adult population with CNS malignancies.

This was a retrospective study performed at a single-center, Cincinnati Children’s Hospital Medical Center. Patients diagnosed with CNS malignancy and managed with CSI between the years 1986–2018 were identified by the Neuro-Oncology Program and included in the study if they had at least one echocardiogram post therapy with digitized images available for review by speckle tracking. Patients who received anthracyclines were excluded from the study. Transthoracic echocardiograms were performed on 1 of 3 ultrasound systems used at our institution during the study period: Vivid 7 (General Electric Healthcare, Milwaukee, WI), iE33 (Phillips Medical Systems, Best, The Netherlands), or Sequoia 512 (Acuson, Oceanside, CA). Demographic, treatment (radiation dosing, anthracycline exposure), and standard echocardiographic data were collected from the electronic medical record for two time periods: “early” representing an echocardiogram performed at < 12 months from the end of therapy, and “late” representing an echocardiogram performed at ≥ 12 months from the end of therapy. Of note, very few patients had echocardiography performed prior to CSI so this time point was not included. For any missing echocardiographic data (i.e., SF and EF), measurements were made retroactively. These data were compared to well-established population normal values.

Myocardial strain is a relatively angle-independent measure of ventricular function, noninvasively measured by echocardiogram or cardiac MRI.¹³ Strain is reported as a percent and can be measured in a global or segmental fashion, in one of three planes: longitudinal (negative value), circumferential (negative value), and radial (positive value). For evaluation of global longitudinal strain (GLS), global circumferential strain (GCS), and global radial strain (GRS) by two-dimensional speckle tracking echocardiography, post-hoc analysis was performed at early and late time points. In brief, Digital Imaging and Communications in Medicine (DICOM) data were analyzed using vendor-independent clinical echocardiographic software (Image Arena, TomTec Imaging Systems, Munich, Germany). Since there are no available normative data for two-dimensional strain in pediatric patients specific to this software, an age-matched control group was generated from individuals referred for echocardiogram for a variety of reasons (e.g., family history of cardiomyopathy, murmur) and ultimately found to have no cardiac pathology.

Data were examined for completeness, distributions were examined for shape, and outliers were checked for feasibility. Cross-checks were done, including by scatterplots, and contingency tables. Any questionable data points were referred back to the source, and any typographical, or other errors in reporting were corrected. Patient characteristics and demographics were displayed in contingency tables, and as means ± standard deviations for continuous variables. A control group was established for each time point by selecting control echocardiographic studies to match patients by age, as closely as possible. Comparisons between controls and patients were done using Fisher’s exact tests for categorical data and continuous variables were tested using Wilcoxon rank-sums analyses. Boxplots were constructed to display differences between control and patient results. Comparisons between early and late results were done using paired t-tests.

A total of 51 patients treated with CSI for CNS malignancies were identified from our database for the years 1986–2018, including 67% (34/51) male and 88% (45/51) white race. The most common diagnosis was medulloblastoma (45/51), with the remaining cases including atypical teratoid, ependymoma, and glioma. Most patients received cisplatin (44/51) and cyclophosphamide (39/51). While almost all patients received craniospinal radiation, 1 received only spinal radiation and 1 received no spinal radiation. The latter patient was excluded from further analysis. Photon therapy was used more often than proton, and more than half of the patients received ≥30 Gy of spinal radiation (Table 1).

Table 1

Patient and disease characteristics at enrollment. N = 50 patients studied.
	Male	Female
Sex	34	17
	White	Black	Asian	Other
Race	45	4	1	1
	Medulloblastoma	Atypical Teratoid	Ependymoma	Glioma	Other
Diagnosis	42	2	1	2	4
	Brain	Spine, cervical	Spine, Thoracic	Spine, Lumbar	Other
Cancer Location*	51	2	1	4	11
	Yes	No
Chemotherapy Used	49	2
	Cisplatin	Cyclophosphamide	Carboplatin	Lomustine	Ifosfamide
Chemotherapy Type	44	39	19	19	1
	Craniospinal	Spinal Only
Radiation Location	50	1
	Photon	Proton	Unknown
Radiation Type	36	14	1
	> 0 to < 30	≥30	None^#	Unknown
Radiation Dose to the spine, Gy	17	29	1	4
*Other locations included: leptomeningeal (5), positive cerebrospinal fluid (4), sacral (2)
^#Patient removed from analysis

Echocardiograms were available in 20 patients at the early time point and 34 patients at the late time point. There were 13 patients with echocardiograms in both groups, however the time points were not compared to each other and considered standalone time points. The oldest echocardiogram included was performed in 2002, and the vast majority were from 2008 or more recent. The patients at the late time point were older than those in the early group (21.7 ± 10.4 vs. 13.3±9.6 years, respectively), and time between end of therapy and echocardiogram was greater (13.1±8.8 vs. 0.2±0.3 years, respectively). Standard echocardiographic parameters assessing LV chamber size, mass, and systolic function were normal for all subjects when compared to age-based published normal values (Table 2). Afterload, represented by systolic blood pressure, was normal for both groups.

Table 2

Demographic and standard echocardiographic measures at early and late timepoints after craniospinal radiation (see text for definition of terms). LV = left ventricular; LVEDD = left ventricular diastolic dimension; LVEF = left ventricular ejection fraction; LVFS = left ventricular fractional shortening; SBP = systolic blood pressure.
	early	late
N	20*	34^#
Age (year)	13.3 ± 9.6	21.7 ± 10.4
Time since therapy completion (year)	0.2 ± 0.3	13.1 ± 8.8
SBP (mmHg)	105.4 ± 10.3	115.2 ± 16.1
LVEDD (mm)	4.0 ± 0.6	3.9 ± 0.6
LVFS (%)	32.6 ± 5.4	34.4 ± 3.8
LVEF (%)	62.3 ± 6.5	60.9 ± 4.5
*N available for analysis: LVEDD = 19; LVEF = 15; all other = 20.
^#N available for analysis: SBP and LVSF = 33; LVEDD and LVEF = 30; all other = 34.

When considering myocardial deformation measured by myocardial strain analysis, at early, CSI vs. control: GLS was − 16.8±3.6% vs. -21.3±4.0% (p=0.0002), GCS was − 22.5±5.2% vs. -21.3±3.4% (p=0.28), and GRS was 21.8±11.0% vs. 26.9±7.7% (p = 0.07) (Table 3). At late, CSI vs. control: GLS was − 16.2±5.4% vs. -21.6±3.7% (p<0.0001), GCS was − 20.9±6.8% vs. -21.9±3.5% (p=0.42), and GRS was 22.5±10.0% vs. 27.3±8.3% (p = 0.03) (Table 3). Because a cut-off of 30 Gy radiation with potential impact to the heart is a known risk factor for development of cardiotoxicity,⁶ we assessed the differential effect of low-dose CSI (< 30 Gy) and high-dose CSI (≥30 Gy) on strain parameters in the study. In addition, with decreased off-target effects reported for proton vs. photon sources of radiation⁴ we assessed whether there was a difference in strain values between patients treated with these two modalities. There were no statistically significant differences between either of these treatment conditions at either time point for any of the strain values (Table 3).

Table 3

Global longitudinal strain (GCS), global circumferential strain (GCS), and global radial strain (GRS) in patients vs. age- and sex-matched controls at early and late (see text for definition), photon vs. proton radiation type, and spinal radiation exposure of < 30 Gy vs. ≥30 Gy.
	early	Control	p-value	late	Control	p-value
N	19	36	--	30	48	--
Male	10 (52%)	23 (64%)	0.56	21 (70%)	31 (65%)	0.81
Age (year)	11.7 ± 8.0	11.3 ± 5.0	0.36	21.7 ± 10.1	20.3 ± 9.6	0.56
GLS*	-16.8 ± 3.6%	-21.3 ± 4.0%	0.0002	-16.2 ± 5.4%	-21.6 ± 3.7%	< 0.0001
GCS*	-22.5 ± 5.2%	-21.1 ± 3.3%	0.28	-20.9 ± 6.8%	-21.9 ± 3.5%	0.42
GRS*	21.8 ± 11.0%	26.9 ± 7.7%	0.07	22.5 ± 10.0%	27.3 ± 8.3%	0.03
	early photon	early proton	p-value	late photon	late proton	p-value
GLS^#	-16.4 ± 2.3%	-17.6 ± 5.1%	0.50	-15.9 ± 5.3%	-16.8 ± 6.3%	0.78
GCS^#	-22.0 ± 5.9%	-23.4 ± 3.6%	0.64	-20.6 ± 7.4%	-21.6 ± 4.6%%	0.77
GRS^#	22.5 ± 11.5%	20.4 ± 10.9%	0.74	22.1 ± 8.8%	24.4 ± 16.0%	0.65
	early < 30 Gy	early ≥30 Gy	p-value	late < 30 Gy	late ≥30 Gy	p-value
GLS^{^}	-17.1 ± 3.9%	-17.1 ± 3.6%	0.50	-15.8 ± 4.5%	-14.9 ± 4.2%	0.72
GCS^{^}	-24.0 ± 5.2%	-20.6 ± 5.9%	0.64	-24.0 ± 8.4%	-20.0 ± 7.1%	0.31
GRS^{^}	26.8 ± 10.1%	15.7 ± 9.1%	0.74	21.3 ± 12.9%	21.2 ± 8.3%	0.99
*N available for analysis: early = 18 GLS, 15 GCS, and 16 GRS; late = 26 GLS, 29 for GCS and GRS.
^#N available for analysis: early photon = 11 GLS and GRS, 10 GCS; early proton = 7 GLS, 5 GCS and GRS; late photon = 23 GLS, 24 GCS and GRS; late proton = 4 GLS, 5 GCS and GRS.
^{^}N available for analysis: early < 30 = 8 for all; early > 30 = 8 GLS, 5 GCS, and 6 GRS; late < 30 = 4 for all; late ≥30 = 20 GLS, 22 GCS and GRS.

Craniospinal irradiation is a common therapeutic option for patients with CNS malignancies. Traditionally, CSI has been associated with improved survival rate in these patients, however it is believed that long-term effects include remodeling of the extracellular matrix yielding fibrosis of the surrounding cardiac tissue.^{14, 15} Recent data from the Childhood Cancer Survivor Study showed a significant reduction in coronary artery disease and a non-significant reduction in cardiomyopathy for survivors of pediatric cancer, largely attributed to historical reductions in cardiac exposure to radiation.¹⁶ In addition efforts have been made to decrease cumulative doses of cardiotoxic chemotherapy agents such as anthracyclines. Despite attempts to reduce therapy while maintaining disease control, survivors of pediatric cancer may show evidence for ventricular dysfunction or subclinical cardiotoxicity.¹⁷

The present study sought to examine the degree of left ventricular systolic dysfunction in patients undergoing CSI by two-dimensional conventional and speckle tracking echocardiography. When compared to an age-matched control group, patients at both early (< 12 months after therapy completion, mean 0.22 years) and late ≥12 months after therapy completion, mean 13.1 years) time points demonstrated depressed GLS in the presence of normal left ventricular EF and SF, evidence of subclinical myocardial dysfunction, while GCS was no different, and GRS only showed a decrease at the later time point. This finding is in line with previous studies showing GLS as a marker of dysfunction in patients receiving chemotherapy with otherwise normal EF.

The diagnosis and management of cardiovascular injury in pediatric patients undergoing CSI may be delayed due to the misconception that this particular cancer-directed therapy results in only long-term cardiovascular side effects due to the absence of studies documenting the clinical and advanced imaging manifestations from craniospinal irradiation. Indeed, current guidelines in pediatrics for the surveillance of cardiovascular disease in patients undergoing CSI call for screening many years after completion of therapy. On the other hand, strain analysis during the past decade has facilitated significant advances in noninvasive myocardial mechanics and cardiac function assessment.¹⁸ Myocardial strain can assess myocardial deformation longitudinally, circumferentially, radially, as well as in the form of twist or torsion, thereby generating data that ought to be taken advantage while assessing early subclinical dysfunction in cancer patients receiving treatment, including radiotherapy.^18–20 Whether this will lead to improved outcomes, particularly in patients undergoing CSI, needs to be determined and is worthy of further investigation.

The current study has several limitations. First, the patients included were treated over a 2-decade period. Therapeutic approach in that time has evolved, and an overall decreased scatter in radiation doses has limited the incidence of cardiotoxicity, and this could decrease the signal for cardiotoxicity in patients treated in the recent era.¹⁶ However, no significant difference was detected between our limited subset of patients who received proton therapy vs. photon at both timepoints. Second, while myocardial strain analysis has been available for better than a decade, it has yet to be regularly employed in pediatric surveillance, and for studies from the first part of the study period there may have been incomplete imaging planes captured to allow for retroactive strain analysis. This contributed to having fewer patients available for strain analysis than for standard echocardiographic assessment. Additionally, in some cases of historic echocardiograms imaging windows limited measurement of some standard parameters. Finally, because echocardiography has not been a regular part of management of this patient group, there were limited cases in which an echocardiogram was performed in the early period after treatment, and even fewer in which a baseline echocardiogram was performed. Simply put, we could not determine if there was a baseline level of cardiac disease in this patient population prior to therapy, nor did we have an appropriate number of patients with studies both early and late after therapy to determine if there was worsening or improvement with time. It is tempting to assume there is no significant disease in this population prior to therapy, however in patients with leukemia there is a baseline increase in troponin and natriuretic peptide that is improved shortly after cancer therapy is initiated, suggesting an underlying state of cardiac stress related to the illness.²¹ Additionally, measures of diastolic function were not included until the most recent few years, and this is known to be an important component to ventricular dysfunction caused by radiation therapy.

Subclinical left ventricular systolic dysfunction demonstrated by GLS is present both early and late after CSI. There is not a clear association between dose and/or type of radiation therapy. These results argue for inclusion of baseline cardiovascular assessment and early initiation of longitudinal follow-up in CNS tumor patients post CSI. Coupled with cardiac biomarkers, this may allow a more complete phenotype of injury related to treatment of CNS tumors in pediatric patients.

CSI craniospinal irradiation

CNS central nervous system

EF ejection fraction

GCS global circumferential strain

GLS global longitudinal strain

GRS global radial strain

MRI magnetic resonance imaging

SF shortening fraction

Ethics approval and consent to participate

The study was approved by the Institutional Review Board at Cincinnati Children’s Hospital Medical Center. There was a waiver of consent for this retrospective study.

Consent for publication

Not applicable.

Availability of data and materials

The datasets during and/or analyzed during the current study available from the corresponding author on reasonable request.

Competing interests

The authors declare that they have no competing interests.

Funding

This research was supported by Divisional funds of the corresponding author (TDR).

Authors’ contributions

HRM conceived and developed the project, collected data, analyzed echocardiograms, interpreted data, and wrote the first draft of the manuscript. RS conceived and developed the project, provided access to the patient population, and provided critical feedback on the manuscript. EW collected data and provided critical feedback on the manuscript. LB collected and managed data. PRK performed all statistical analyses and provided critical feedback on the manuscript. JTT provided echocardiographic expertise, developed the control population, and provided critical feedback on the manuscript. TDR conceived and developed the project, interpreted data, and oversaw writing of all drafts of the manuscript. All authors read and approved the final manuscript.

Acknowledgements

Thank you to Vicky Moore, RDCS, FASE for assistance in performing strain analysis.

Miller KD, Siegel RL, Lin CC, Mariotto AB, Kramer JL, Rowland JH, Stein KD, Alteri R, Jemal A. Cancer treatment and survivorship statistics, 2016. CA Cancer J Clin. 2016;66:271–89.
Ward E, DeSantis C, Robbins A, Kohler B, Jemal A. Childhood and adolescent cancer statistics, 2014. CA Cancer J Clin. 2014;64:83–103.
Lipshultz SE, Adams MJ, Colan SD, Constine LS, Herman EH, Hsu DT, Hudson MM, Kremer LC, Landy DC, Miller TL, Oeffinger KC, Rosenthal DN, Sable CA, Sallan SE, Singh GK, Steinberger J, Cochran TR, Wilkinson JD, American Heart Association Congenital Heart Defects Committee of the Council on Cardiovascular Disease in the Young. CoBCSCoC and Stroke Nursing CoCR. Long-term cardiovascular toxicity in children, adolescents, and young adults who receive cancer therapy: pathophysiology, course, monitoring, management, prevention, and research directions: a scientific statement from the American Heart Association. Circulation. 2013;128:1927–95.
Welch GD, Lin KY, Fisher MJ, Hill-Kayser CE. Cardiac Toxicity After Craniospinal Irradiation: A Late Effect That May be Eliminated With Proton Therapy. J Pediatr Hematol Oncol. 2018;40:e330–3.
De Saint-Hubert M, Verellen D, Poels K, Crijns W, Magliona F, Depuydt T, Vanhavere F, Struelens L. Out-of-field doses from pediatric craniospinal irradiations using 3D-CRT, IMRT, helical tomotherapy and electron-based therapy. Phys Med Biol. 2017;62:5293–311.
Armenian SH, Hudson MM, Mulder RL, Chen MH, Constine LS, Dwyer M, Nathan PC, Tissing WJ, Shankar S, Sieswerda E, Skinner R, Steinberger J, van Dalen EC, van der Pal H, Wallace WH, Levitt G. Kremer LC and International Late Effects of Childhood Cancer Guideline Harmonization G. Recommendations for cardiomyopathy surveillance for survivors of childhood cancer: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group. Lancet Oncol. 2015;16:e123-36.
Konstam MA, Abboud FM. Ejection Fraction: Misunderstood and Overrated (Changing the Paradigm in Categorizing Heart Failure). Circulation. 2017;135:717–9.
Frommelt PC, Minich LL, Trachtenberg FL, Altmann K, Camarda J, Cohen MS, Colan SD, Dragulescu A, Frommelt MA, Johnson TR, Kovalchin JP, Lin L, Mahgerefteh J, Nutting A, Parra DA, Pearson GD, Pignatelli R, Sachdeva R, Soriano BD, Spurney C, Srivastava S, Statile CJ, Stelter J, Stylianou M, Thankavel PP, Tierney ES, van der Velde ME. Lopez L and Pediatric Heart Network I. Challenges With Left Ventricular Functional Parameters: The Pediatric Heart Network Normal Echocardiogram Database. J Am Soc Echocardiogr. 2019;32:1331–8. e1.
Ramlogan S, Aly D, France R, Schmidt S, Hinzman J, Sherman A, Goudar SP, Forsha D. Reproducibility and Intervendor Agreement of Left Ventricular Global Systolic Strain in Children Using a Layer-Specific Analysis. J Am Soc Echocardiogr. 2020;33:110–9.
Akam-Venkata J, Kadiu G, Galas J, Lipshultz SE, Aggarwal S. Left ventricle segmental function in childhood cancer survivors using speckle-tracking echocardiography. Cardiol Young. 2019;29:1494–500.
Pignatelli RH, Ghazi P, Reddy SC, Thompson P, Cui Q, Castro J, Okcu MF, Jefferies JL. Abnormal Myocardial Strain Indices in Children Receiving Anthracycline Chemotherapy. Pediatr Cardiol. 2015;36:1610–6.
Thavendiranathan P, Poulin F, Lim KD, Plana JC, Woo A, Marwick TH. Use of myocardial strain imaging by echocardiography for the early detection of cardiotoxicity in patients during and after cancer chemotherapy: a systematic review. J Am Coll Cardiol. 2014;63:2751–68.
Amzulescu MS, De Craene M, Langet H, Pasquet A, Vancraeynest D, Pouleur AC, Vanoverschelde JL, Gerber BL. Myocardial strain imaging: review of general principles, validation, and sources of discrepancies. Eur Heart J Cardiovasc Imaging. 2019;20:605–19.
Yarnold J, Brotons MC. Pathogenetic mechanisms in radiation fibrosis. Radiother Oncol. 2010;97:149–61.
Delanian S. [Late complications of radiotherapy. Physiopathological aspects of radiation-induced fibrosis]. Bull Cancer Radiother. 1995;82:88–93.
Mulrooney DA, Hyun G, Ness KK, Ehrhardt MJ, Yasui Y, Duprez D, Howell RM, Leisenring WM, Constine LS, Tonorezos E, Gibson TM, Robison LL, Oeffinger KC, Hudson MM, Armstrong GT. Major cardiac events for adult survivors of childhood cancer diagnosed between 1970 and 1999: report from the Childhood Cancer Survivor Study cohort. BMJ. 2020;368:l6794.
Ness KK, Plana JC, Joshi VM, Luepker RV, Durand JB, Green DM, Partin RE, Santucci AK, Howell RM, Srivastava DK, Hudson MM, Robison LL, Armstrong GT. Exercise Intolerance, Mortality, and Organ System Impairment in Adult Survivors of Childhood Cancer. J Clin Oncol. 2020;38:29–42.
Venneri L, Zoppellaro G, Khattar RS. Cardio-oncology: the role of advanced echocardiography in cancer patients. Expert Rev Cardiovasc Ther. 2018;16:249–58.
Larsen CM, Mulvagh SL. Cardio-oncology: what you need to know now for clinical practice and echocardiography. Echo Res Pract. 2017;4:R33–41.
Yu AF, Raikhelkar J, Zabor EC, Tonorezos ES, Moskowitz CS, Adsuar R, Mara E, Huie K, Oeffinger KC, Steingart RM, Liu JE. Two-Dimensional Speckle Tracking Echocardiography Detects Subclinical Left Ventricular Systolic Dysfunction among Adult Survivors of Childhood, Adolescent, and Young Adult Cancer. Biomed Res Int. 2016;2016:9363951.
Lipshultz SE, Miller TL, Scully RE, Lipsitz SR, Rifai N, Silverman LB, Colan SD, Neuberg DS, Dahlberg SE, Henkel JM, Asselin BL, Athale UH, Clavell LA, Laverdiere C, Michon B, Schorin MA, Sallan SE. Changes in cardiac biomarkers during doxorubicin treatment of pediatric patients with high-risk acute lymphoblastic leukemia: associations with long-term echocardiographic outcomes. J Clin Oncol. 2012;30:1042–9.

Download PDF

Journal Publication

published 02 Feb, 2021

Read the published version in Cardio-Oncology →

Editorial decision: Major Revision
24 Dec, 2020
Review #2 received at journal
23 Dec, 2020
Review #1 received at journal
19 Dec, 2020
Reviewer #2 agreed at journal
10 Dec, 2020
Reviewer #1 agreed at journal
08 Dec, 2020
Reviewers invited by journal
07 Dec, 2020
Editor assigned by journal
05 Dec, 2020
Submission checks completed at journal
05 Dec, 2020
Editor invited by journal
05 Dec, 2020
First submitted to journal
03 Dec, 2020

You are reading this older preprint version

Read the latest preprint version →

Echocardiographic Myocardial Strain Analysis Describes Subclinical Cardiac Dysfunction after Craniospinal Irradiation in Pediatric and Young Adult Patients with Central Nervous System Tumors

Status:

Journal Publication

Version 1

Abstract

Introduction

Methods

Results

Discussion

Conclusion

Abbreviations

Declarations

References

Status:

Journal Publication

Version 1