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Blood test may predict who suffers from radiation therapy

NCT ID NCT00893035

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a blood test measuring how certain immune cells die after radiation can predict long-term side effects in breast and prostate cancer patients. Researchers enrolled 885 participants and tracked late complications. The goal is to personalize treatment to reduce harm.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a simple blood test that helps doctors personalize radiation doses to reduce long-term side effects.
What could go wrong
This is an observational study, not a treatment trial. The test may not prove accurate enough for routine use, and results may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

885 people

The number who actually took part.

Start date

Jun 2006

Finished

Oct 2019

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

patients treated in a cancer center

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria for prostate cancer patients: * localised prostate cancer, histologically proven * Absence of metastases (M0) : normal bone scintigraphy * Absence of radiological lymph node invasion (N0). * Clinical Stage : T ≥ T1c-T2a and \< T3b Or T1b or c with PSA ≤ 10 ng/ml . Or T1b or c with Gleason ≥ 6 * PSA \< 30 ng/ml. * Signs and symptoms according to NCI/CTC v3.0 \< grade 2 * ECOG Performance status ≤ 1 * Absence of hip prothesis * Absence de endopenian stent * Patient aged \> 18 and \< 80 * Patient affiliated with social security * Written informed consent, dated and signed Exclusion Criteria for prostate cancer patients: * Antecedents of invasive cancer (unless if treated more than 5 years ago without evolution) except basocellular carcinoma * positive biopsy of seminal vesicle * PSA ≥ 30 ng/ml for two successive dosages * Previous pelvic irradiation * Previous radical prostatectomy for cancer * Patients with another systemic disease (cardiovascular, renal, hepatic, pulmonary embolism, etc.) non stabilised or generalised sclerodermitis. * Patients known to be HIV seropositive (no specific test is necessary for defining eligibility) * Known homozygote ATM (Ataxy telangiectasy) mutation * Impossibility for a correct follow up (for social family or geographical reasons) * Patients incapable of providing consent, protected majors, vulnerable persons * Patients participating in other clinical trials Inclusion Criteria for breast cancer patients: * Breast Conservative surgery * Non metastatic, M0 * negative surgical margins * T1, T2; negative sentinel lymph node N0, N1 or N2. * Signs and symptoms according to NCI/CTC v3.0 \< grade 2 * Patient aged over 18 years and less than 60 or more than 60 with an indication for boost irradiation. * Patient affiliated with social security * Written informed consent, dated and signed Exclusion Criteria for breast cancer patients: * Metastatic patients * Bilateral breast cancer (concomitant or previous) except in situ * T4 or N3 or treated by mastectomy * Patients with chemotherapy or neoadjuvant hormonotherapy * Patients with a previous other cancer within the last 5 years EXCEPT basocellular carcinoma of the skin or in situ cancer of the uterus. * Patients with another systemic disease (cardiovascular, renal, hepatic, pulmonary embolism, etc.) non stabilised or generalised sclerodermia. * Pregnant or breast feeding women * Patients known to be HIV seropositive (no specific test is necessary for defining eligibility) * Known homozygote ATM (Ataxy telangiectasy) mutation * Impossibility for a correct follow up (for social family or geographical reasons) * Patients incapable of providing consent, protected majors, vulnerable persons * Patients participating in other clinical trials

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CRLC Val d'Aurelle

    Montpellier, 34000, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.