Non-small Cell Lung Cancer Clinical Trial
Official title:
An Observational Study of the Correlation Between Cancer-related Fatigue, Survival and Physiological Factors in Non-Small Cell Lung Cancer (NSCLC) Patients Under Chemotherapy
Worldwide, non-small cell lung cancer (NSCLC) is one of the most common causes of cancer
mortality. Also, the first leading cause of death is lung cancer in Taiwan 2012. Most
patients are diagnosed at advanced stages and their median survival with supportive care is
only 3-6 months. The common regimens used on advanced NSCLC treatment consists of
platinum-based doublet chemotherapy, the survival benefit of which is able to extend the
survival to approximately 10 months. However, disease and treatment-related toxicities in
cancer patients may result in fatigue and interfered quality of life (QoL). According to the
others reports, eight QoL areas including physical functioning, fatigue, pain, and appetite
loss have been showed a statistically significant association with survival rate of NSCLC
patients.
Cancer-related fatigue (CRF), an indicator of QoL, has been reported as the most frequent and
distressing toxicity of lung cancer chemotherapy. Proposed criteria for CRF have been adopted
for inclusion in the International Statistical Classification of Disease and Related Health
Problems, Tenth Revision, Clinical Modification (ICD-10-CM). Therefore, more in-depth
researches on CRF are needed in Taiwan.
In addition, electrolyte disturbance like hyponatremia has been reported to be counted as one
of the many contributing factors for fatigue in palliative care patients and associated with
poorer overall survival rate (OS) in lung cancer. Thus, the correlation between CRF and
electrolyte possibly would be a strong link for physician to improve the QoL and survival
rate of NSCLC patients.
The objective of this observational study is to evaluate the correlation between CRF,
survival and physiological factors in NSCLC patients under chemotherapy. The study will
compare the effect of QoL and CRF on survival with or without CRF treatment and investigate
the correlation between the variation of CRF and physiological factors which have been
examined and recorded on medical record under clinical practice. These results will supply
physicians with more understanding about CRF, and help them to enhance the quality on lung
cancer care to being perfected in the future.
Non-small cell lung cancer (NSCLC) patients with chemotherapy will be enrolled. Patients will be thoroughly informed about all aspects of the study activity schedule and all regulatory requirements that must be satisfied for informed consent. Only patients who give consent to participate in this study and meet all other inclusion and exclusion criteria will be eligible to enroll into this study. ICD-10 fatigue criteria, Brief Fatigue Inventory-Taiwan Form (BFI-T), the visual analog scale (VAS) for appetite and Functional Assessment of Cancer Therapy-General quality of life questionnaire (FACT-G7) will be used to evaluate patients' fatigue and quality of life. Patients who enrolled in this observational study will complete the evaluation and questionnaire of fatigue and quality of life according to clinical schedule. The first survey (baseline) will be collected after enrollment, the further surveys will be completed every three chemotherapy cycles following subject's chemotherapy schedule and after finish the whole course of chemotherapy. Subject demographic and disease-related information and routine laboratory data will also be collected from medical record for analysis. ;
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