RecruitingNot ApplicableNCT01993498

Chronic Toxicities Related to Treatment in Patients With Localized Cancer

A Prospective Cohort to Investigate Survivorship Issues in Patients With Early Cancer


Sponsor

UNICANCER

Enrollment

14,750 participants

Start Date

Feb 20, 2012

Study Type

INTERVENTIONAL

Conditions

Summary

The aims of the cohort will be to quantify impact of cancer treatments toxicities , and to generate predictors of chronic toxicity in patients with non-metastatic cancer. Study of the original cohort will be focused on localized breast cancer patients, other localisation in non-metastatic setting will be explored furtherwise, fist of all in lung cancer. The project will include four specific aims : 1. To develop a database of chronic treatment related toxicity in a cohort of 14750 women with stage I-III breast cancer (= non metastatic), whatever these treatments are (surgery; radiation therapy; chemotherapy …) 2. To describe incidence, clinical presentation, and outcome of chronic toxicities. 3. To describe the psychological, the social and the economic impacts of chronic toxicities. 4. To generate predictors for chronic toxicities in order to prevent them, based upon biological criteria. The expected impact of these toxicities, when identified, will be to improve quality of life and to decrease health cost, by the early identification of patients at high risk of toxicity. Such early identification could lead to prevent toxic effect by: a. developing prevention strategies, b. substituting toxic treatment by a non (less) toxic one. Also, such cohort will offer a quantification of the impact of treatment toxicity, that could be further used to quantify medical usefulness of strategies that aim at decreasing treatment toxicities (implementation of predictive biomarker for resistance, cytotoxic-free regimen etc…)


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is tracking long-term side effects of breast and lung cancer treatment in France, to better understand how cancer treatment affects quality of life over time. You may be eligible (for the breast cancer group) if: you are a woman 18 or older with a new invasive breast cancer diagnosis; the cancer has not spread to other parts of the body; you have not yet started cancer treatment; and you speak French. You may be eligible (for the lung cancer group) if: you are 18 or older with a confirmed or suspected early-stage lung cancer diagnosis (no spread); you are eligible for surgery or radiation treatment; and you have not yet received treatment. You may NOT be eligible if: your cancer has already spread; you have had cancer in the past 3–5 years (depending on type); you have already received treatment; or you do not speak French. Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREblood sampling

blood samples collection


Locations(1)

Gustave roussy

Villejuif, France

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NCT01993498


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