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

This trial does not accept healthy volunteers

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 population

Patients planned to be treated with radiotherapy and who are receiving a targeted therapy, including immunotherapy.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Radiotherapy

    Radiation

    Combined modality

Treatment groups

3,600 Participants
are divided into 1 treatment group
Group A: Combined modality1 intervention

Trial outcomes

Primary outcomes

1

Number of Participants with severe side effects

CTCAE V5 Grade 3-5 toxicities

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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