pediatric cancer survivors
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Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 840-840
Author(s):  
Xu Ji ◽  
Xin Hu ◽  
Joseph Lipscomb ◽  
Ann Mertens ◽  
Sharon M. Castellino

Abstract Background: The Children's Oncology Group Long-Term Follow-up Guidelines recommend surveillance for late effects in pediatric cancer survivors based on therapeutic exposures. In particular, the Guidelines recommend an echocardiogram, or comparable imaging, every 2 to 5 years to evaluate cardiac function in survivors exposed to anthracycline chemotherapy. However, little is known about the real-world utilization of cardiac surveillance tests following the completion of cancer therapy. Objective: This study fills this gap by describing the proportion of anthracycline-treated survivors of pediatric cancer who received surveillance for cardiac function following the completion of their cancer therapy. Method : We developed an algorithm to identify a cohort of pediatric cancer survivors using the IBM MarketScan ® Commercial Claims and Encounters Database (a nationwide private insurance enrollment and claims database). The cohort for inclusion was enrollees who (1) received anthracycline for blood cancer (leukemia or lymphoma); (2) aged ≤21 years at cancer diagnosis; (3) completed all cancer therapy between 2009 and 2018; and (4) remained continuously insured for at least one year post-therapy. Outcomes assessed included the receipt of: (1) echocardiogram, (2) cardiac magnetic resonance imaging (MRI), (3) multiple gate acquisition (MUGA) scan, and (4) any of the aforementioned cardiac surveillance tests over the 5-year period after the completion of all cancer therapy. The Kaplan-Meier (K-M) method was used to estimate the cumulative incidence of an event post-therapy, where the event was defined as the initial healthcare claim for a cardiac surveillance test. Individuals were censored if they had not received a test by study termination or were lost to follow-up at any time during the 5 years post-therapy. Multivariate Cox proportional hazard models were estimated to identify the demographic and cancer-related factors strongly associated with the initial test receipt. Results : Among 1,914 eligible blood cancer survivors, 259 (13.5%) survivors received a hematopoietic stem cell transplantation (HSCT; Table 1). The K-M estimated probability of receiving a cardiac surveillance test by 5 years post-therapy was 61.0% (95% Confidence Interval [CI]: 57.2% to 64.7%), with the median time to the initial test being 2.6 years (95% CI: 2.2 to 3.1 years) from therapy completion. The vast majority of cardiac surveillance test users underwent an echocardiogram (n=850; versus only 10 who had a cardiac MRI, and 14 who had a MUGA scan) by the end of their follow-up period. The proportion of survivors who had an initial cardiac test increased over time but varied by age at cancer therapy completion and the receipt of HSCT. The K-M estimated probability of receiving an initial test by 5 years post-therapy was: 86.0% (95% CI: 77.3% to 91.6%) for children (ages ≤11 years), 85.0% (95% CI: 75.4% to 91.1%) for adolescents (ages 12-17 years), and 36.8% (95% CI: 32.6% to 41.0%) for young adults (ages 18-28 years; Figure 1). Multivariate Cox models showed that compared with children, adolescents were more likely to receive an initial cardiac test (Hazard Ratio [HR] = 1.3; 95% CI: 1.1 to 1.5), while young adults were less likely to receive a test (HR = 0.4; 95% CI: 0.3 to 0.5). In addition, survivors who received a HSCT were more likely than those who did not to complete an initial cardiac test (HR=1.8; 95% CI: 1.5 to 2.2). Conclusions: This nationwide, claims data-based study showed that a substantial proportion of anthracycline-exposed survivors of blood cancers had not completed a cardiac surveillance test within 5 years post-therapy. Within this high-risk population, young adults were significantly less likely to receive surveillance testing for the prevention and early detection of cardiac dysfunction. Figure 1 Figure 1. Disclosures No relevant conflicts of interest to declare.


2021 ◽  
Vol 61 ◽  
pp. 130-135
Author(s):  
Haiying Huang ◽  
Yingwen Wang ◽  
Xiaorong Mao ◽  
Xiuli Qin ◽  
Lei Cheng

Author(s):  
Rachel Peterson ◽  
Lisa Jacobson

Objective. Pediatric oncology survivors are at risk for executive function (EF) and working memory (WM) deficits, which can be measured via performance-based measures or rating scales. Previous studies have shown these measurement methods to be weakly correlated. This study aimed to describe parent rated EF and performance-based working memory (PBWM) in pediatric cancer survivors; examine change in EF and PBWM across time; and investigate the relationship between parent rated WM and PBWM. Method. The sample included 59 patients (50 brain tumor, 9 Leukemia) diagnosed in childhood (Mage=6.92 years; SD=4.12) seen twice for clinical neuropsychological evaluation. PBWM was examined via the auditory working memory scale from a Wechsler intelligence measure or Differential Ability Scales-II. Parents completed the BRIEF/2 as a measure of global EF (GEC), metacognitive skills (MI/CRI), and behavioral regulation (BRI). Results. MI/CRI and GEC at Time 1 were significantly above the mean (p<.01), while PBWM did not differ from the normative mean. GEC, MI/CRI, and BRI were significantly higher than the normative mean at Time 2 (p<.05). PBWM was both clinically and statistically elevated (p<.001). There was a significant change across time in GEC, MI/CRI, and PBWM (p<.05), but not BRI. PBWM was only weakly correlated with the BRIEF WM subscale at Time 1 and Time 2 (all p>.05). Conclusions. Multiple measures of EF should be considered when providing diagnoses and recommendations for pediatric cancer survivors. Furthermore, given declines across time, findings document need for continued monitoring and re-assessment of pediatric survivors as they get further out from treatment.


2021 ◽  
Author(s):  
Müberra Tanrıverdi ◽  
Fatma Betül Çakır

Abstract Aim Cancer-related long term complications such as cardiovascular disease, fatigue, weight-related problems, and emotional disturbances are found to be increased in pediatric cancer survivors (PCS). The relationship between daily living activities (DLA) and such complications is still being investigated. Our aim in this study was to investigate the impact of cancer-related fatigue on DLA in PCS. Methods Cancer-related fatigue was assessed by “PedsQL Multidimensional Fatigue Scale (MFS)”, “Visuel Analogue Scale (VAS)” and “Borg Fatigue Scale”. The DLA was evaluated by WeeFIM. Results There were 77 PCS (44 boys) with a mean age of 10.76 ± 4.49 years. The mean value of fatigue scales were VAS 2.48 ± 1.48, Borg 0.61 ± 1.00 and MFS total score 71.14 ± 18.74. There was a statistically significant negative relationship between age and VAS scores of PCS (p = 0.047). The girls were found more tired than boys (VAS; p = 0.031). A positive correlation was established between the type of tumor and MFS total score (p = 0.048). WeeFIM total result was 118.64 ± 11.37. While there was a statisticially significant relationship between VAS Fatigue Score and WeeFIM total (p = 0.07), there was no such correlation between MFS total and WeeFIM total (p = 0.080) and Borg Fatigue Scale and WeeFIM total (p = 0.449). Conclusions It is established that there is a relationship between level of fatigue and DLA. Risk factors like tumor type or treatment modalities for fatigue should be investigated in larger samples of specific survivor groups. Fatigue and its association with DLA should be screened clinically as a routine surveillence in PCS and treatment options be planned.


Author(s):  
Mona L. Peikert ◽  
Laura Inhestern ◽  
Konstantin A. Krauth ◽  
Gabriele Escherich ◽  
Stefan Rutkowski ◽  
...  

Abstract Purpose Recent research demonstrated that fear of progression (FoP) is a major burden for adult cancer survivors. However, knowledge on FoP in parents of childhood cancer survivors is scarce. This study aimed to determine the proportion of parents who show dysfunctional levels of FoP, to investigate gender differences, and to examine factors associated with FoP in mothers and fathers. Methods Five hundred sixteen parents of pediatric cancer survivors (aged 0–17 years at diagnosis of leukemia or central nervous system (CNS) tumor) were consecutively recruited after the end of intensive cancer treatment. We conducted hierarchical multiple regression analyses for mothers and fathers and integrated parent-, patient-, and family-related factors in the models. Results Significantly more mothers (54%) than fathers (41%) suffered from dysfunctional levels of FoP. Maternal FoP was significantly associated with depression, a medical coping style, a child diagnosed with a CNS tumor in comparison to leukemia, and lower family functioning (adjusted R2 = .30, p < .001). Paternal FoP was significantly associated with a lower level of education, depression, a family coping style, a child diagnosed with a CNS tumor in comparison to leukemia, and fewer siblings (adjusted R2 = .48, p < .001). Conclusions FoP represents a great burden for parents of pediatric cancer survivors. We identified associated factors of parental FoP. Some of these factors can be targeted by health care professionals within psychosocial interventions and others can provide an indication for an increased risk for higher levels of FoP. Implications for Cancer Survivors Psychosocial support targeting FoP in parents of childhood cancer survivors is highly indicated.


Author(s):  
Rebecca Williamson Lewis ◽  
Karen E. Effinger ◽  
Karen Wasilewski-Masker ◽  
Ann Mertens ◽  
Canhua Xiao

2021 ◽  
pp. JCO.20.02471
Author(s):  
Jordan Gilleland Marchak ◽  
Katie A. Devine ◽  
Melissa M. Hudson ◽  
Lisa A. Jacobson ◽  
Gisela Michel ◽  
...  

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