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some studies with psychological distress and somatization (Schultz et al., 2007;<br />
Vannatta et al., 2007). In this study, CNS directed therapy including radiation and<br />
intrathecal chemotherapy was not linked to poorer reports of psychosocial functioning,<br />
which was unexpected. Based on the existing literature and our knowledge of the<br />
medical and neurological late effects that a number of these young people have, we<br />
expected the difficulties to be apparent, reaching a level of significance. One<br />
explanation that may account in part for this was suggested by Vannatta et al. (2007),<br />
who reported that while children who received CNS therapy with neurotoxic late effects<br />
had more peer problems and were more socially isolated, they did not report problems<br />
with social functioning to the same degree as parents or teachers and suggested that<br />
limited self-awareness of social difficulties was a factor. Other possible contributing<br />
factors are discussed later in this chapter.<br />
Higher rates of depression following a childhood cancer diagnosis and some<br />
treatment modalities specifically CNS irradiation and HSCT, have been identified as<br />
being a significant issue for this group of young people in a number of studies (Schultz<br />
et al., 2007; Vannatta et al., 2007; Zeltzer et al., 2009). This was not found in this<br />
survey. Depression as defined by the RADS2-SF was seen in approximately 6% of<br />
those who completed the survey and there was no correlation to gender, ethnicity,<br />
disease or treatment modality. While the numbers reporting significant depression were<br />
low in this survey, it is important to acknowledge that for those that did so, it is<br />
clinically important. In addition, as suggested by DeJong and Fombonne (2006), any<br />
level of depression is pertinent as subclinical levels have been shown to have a negative<br />
effect on quality of life, social relationships and compliance with heath interventions.<br />
5.2 Comparison of Childhood Cancer Survivors and Youth’07 Sample<br />
Youth’07 (Y’07) was a national health survey of a representative sample of<br />
college students in New Zealand. The rates of participation, as a percentage, were very<br />
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