Longitudinal Assessment of Health-Related Quality of Life in Men With Localized Prostate Cancer



Status:Active, not recruiting
Conditions:Prostate Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:Any
Updated:6/6/2018
Start Date:May 2002
End Date:May 2019

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The purpose of this study is to assess quality-of-life of men with prostate cancer.
"Quality-of-life" means how you feel about your life as a result of your disease and its
treatment. The investigators hope that this questionnaire will help show how prostate cancer
treatments affect quality-of-life. It will help doctors and future patients to make better
treatment choices. Some men may wish to have a more demanding treatment with a higher risk of
harmful effects. Others may prefer a treatment that will have the smallest effect on their
quality-of-life.

This questionnaire will help us measure these effects and decide which is the best treatment
for a given patient.

The intent of the protocol is to assess health-related quality-of-life (HRQOL) in men treated
for localized prostate cancer with 1 of 6 established management alternatives: external
(XRT)or interstitial radiotherapy (IRT), open radical prostatectomy (RP), laparoscopic
radical prostatectomy (LRP), combined radiotherapy and brachytherapy (Combined RT) or
watchful waiting (WW). HRQOL is an important aspect of any treatment for prostate cancer due
to the beliefs by many that cancer control rates are similar across common modalities and
HRQOL reduction from treatment is substantial (1-5). Therefore, HRQOL appears to occupy a
central role in the decision making process related to treatment selection.

Inclusion Criteria:

- diagnosis of localized, untreated prostate cancer (clinical stages T1-3, Nx, M0)

- ability to read the English language

Exclusion criteria:

- other cancer diagnosis for the past three years, except for non-melanoma skin cancer

- prior chemotherapy within the last three years; radiation therapy to the pelvis or
prior pelvic surgery within the past three years

- prior neoadjuvant therapy, such as hormones (Bicalutamide use for less than or equal
to 1 month would not constitute exclusion from study entry)

For the cross-sectional component of the study, all patients identified to be free of
disease at least ten years post -treatment will be considered eligible. Patients must have
no clinical evidence of local, regional or distant recurrences. Patients must have the
ability to read and understand English. Patients who received hormonal therapy will be
eligible for the cross-sectional component of the study, but the duration of the hormonal
therapy must be six months or less. the investigators have identified a cohort of patients
who fit these criteria from our databases.
We found this trial at
5
sites
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Sleepy Hollow, NY
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Basking Ridge, New Jersey
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Basking Ridge, NJ
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Commack, NY
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1275 York Ave
New York, New York 10021
(212) 639-2000
Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...
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New York, NY
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1000 N Village Ave
Rockville Centre, New York 11570
(516) 256-3600
Memorial Sloan-Kettering at Mercy Medical Center Memorial Sloan Kettering Cancer Center Rockville Centre provides state-of-the-art...
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Rockville Centre, NY
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