Quality of Life in Patients After Combined Modality Treatment of Rectal Cancer

Institute of Oncology Ljubljana

Status: Unknown

Conditions: Rectal Cancer

Treatments: Behavioral: questionnaires

Study type: Observational

Funder types: Other

Identifiers

NCT01152164

125/08

Details and patient eligibility

About

The goal of this study is gathering informations about patients' quality of life after combined modality treatment of rectal cancer to evaluate how combined modality treatment for rectal cancer affects patients' quality of life. The findings of this study may provide us important information that can be used in treatment decision and to develop programs to improve quality of life of patients with rectal cancer.

Full description

Over the last two decades, rectal cancer research has lead to better understanding of disease behaviour, resulting in more efficient treatments and higher prevalence of cancer survivors.Due to aggressive therapy, rectal cancer survivors can exhibit late sequelae of treatment, most common being impaired bowel, voiding, sexual malfunctioning and quality of life impairment. In order to determine the impact of rectal cancer and its treatment on patients' quality of life over time, this study will prospectively follow a cohort of patients at specified intervals evaluating their physical symptoms, physical and social functioning and overall quality of life.Medical and sociodemographic factors that might be predictive will be tested.

Enrollment: 167 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• histologically verified adenocarcinoma of the rectum,
• clinical stage II or III (IUCC TNM classification 2002);
• no prior radiotherapy and/or chemotherapy;
• World Health Organisation (WHO) performance status < 2;
• age at diagnosis of 18 or older;
• and adequate bone marrow, liver, renal and cardiac function (no history of ischemic heart disease)
• mentally fit to complete questionnaires

Exclusion criteria

• a history of prior malignancy other than non-melanoma skin cancer or in situ carcinoma of the cervix rendered the patient ineligible.

Trial design

167 participants in 1 patient group

rectal cancer patients

Treatment:

Behavioral: questionnaires