Cancer Cachexia Clinical Trial
Official title:
Neuroimaging of Hypothalamic Activity During Cancer Anorexia
The pathogenesis of cancer anorexia is complex and multifactorial. However, a number of
consistent and robust evidence point to a prominent role for the central nervous system. In
particular, the hyperactivation of the immune system, due to tumour growth, causes a
systemic inflammatory response primarily mediated by pro-inflammatory cytokines. At the
central level, inflammatory response profoundly alters the activity of the hypothalamic
nuclei, which are involved in the regulation of energy homeostasis. In particular,
pro-inflammatory cytokines inhibit prophagic neurons activity, while enhance the activation
of the anorexigenic neurons. Although supported by compelling experimental evidence, it
should be acknowledged that this pathogenic hypothesis has not been confirmed yet by human
studies.
Aim of the present study is to determine the specific pattern(s) of the brain activation
after assumption of a standard meal in both anorexic and non-anorexic cancer patients to
reveal potential differences, which will be correlated with the levels of concurrently
measured circulating pro-inflammatory cytokines. The results obtained would help in
assessing the role of the central nervous system and, in particular of the hypothalamus, in
the pathogenesis of cancer anorexia.
After approval of the study protocol by the Ethical Committee of our Institution (Azienda
Policlinico Umberto I, Sapienza University, Rome, Italy), 9 anorexic cancer patients, 4
non-anorexic cancer patients and 2 healthy individuals will be studied. The sample size is
based on studies of neuroimaging already published and available on international journals.
Patients with confirmed cancer diagnosis will be enrolled before the initiation of any
anti-cancer treatments. The presence/absence of anorexia will be investigated using a
specific questionnaire (Cangiano et al., 1990) and a visual analogue scale (VAS). After an
overnight fasting, blood samples will be collected from cancer patients and control subjects
and interleukin(IL)-1, IL-6 and Tumor Necrosis Factor-α (TNF-α) levels will be measured by a
commercially available ELISA kit.
On the same day, hypothalamic activation pattern(s) will be evaluated in patients and in
control subjects by fMRI. After basal evaluation, all the groups will receive a standard
oral meal, i.e., a 200 mL hypercaloric oral nutritional supplement providing 300 Kcal, and
then a second fMRI scan will be performed. Using a computerized software, the average value
of the grey for the hypothalamus will be calculated, and normalized for the one obtained in
the basal condition, to obtain the percentage (%) of activation (or inhibition) of the
hypothalamus.
Data obtained will be statistically analyzed using the t-Student and Bonferroni tests.
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Observational Model: Case Control, Time Perspective: Cross-Sectional
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