Attribution of Toxicities Due to Radiotherapy and Immuno-Biological Therapies

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre hospitalier de l'Université de Montréal (CHUM)

About this trial

Every year, new molecular agents enter the market with more and more patients receiving these treatments, especially in the metastatic setting. These molecular agents could correspond to immunotherapy and modulators of signaling pathways. More than 50% of cancer patients will receive radiation therapy during the course of their illness, including radiotherapy aimed a palliating symptoms secondary to metastatic diseases. Therefore, there will be an increasing number of patients who will be receiving radiotherapy while they are still receiving molecular agents. A better understanding of the interaction of these two treatment modalities is needed.

Eligibility criteria

Qualifiers

Consent to be part of the AtTRIBut registry

Prior histological diagnosis of primary cancer.

If the patient has metastatic disease, there must be radiological or pathological evidence of metastasis

Age> 18 years

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Radiotherapy

Treatment groups

3,600 Participants
are divided into 1 treatment group