Stereotactic Ablative Radiotherapy for Oligo-Progressive Non Small Cell Lung Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre hospitalier de l'Université de Montréal (CHUM)

About this trial

A registry-based randomized screening phase II trial. A total of 68 patients with metastatic non small cell lung cancer on systemic therapy with oligoprogression to 1-5 extracranial lesions will be randomized using a 1:1 ratio to standard of care (begin next-line systemic therapy, best supportive care, continue current systemic line, based on treating physician decision) vs. receive stereotactic ablative radiotherapy to all oligoprogressive lesions while continuing their current systemic therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

Metastatic NSCLC enrolled in our CRCHUM Lung Cancer Registry and co-enrolled to the PERa registry

Ability to provide written informed consent

Eastern Cooperative Oncology Group (ECOG) performance status 0-3

Disqualifiers

Any lesion beyond 5 cm

Pregnancy or breastfeeding

Any medical condition that could, in the opinion of the investigator, preclude radiotherapy or prevent follow-up after radiotherapy.

Presence of spinal cord compression Metastatic disease that invades the GI tract (including esophagus, stomach, small or large bowel)

Trial design

Design model

Parallel

Treatments tested in this trial

  • SABR

    Radiation

    SABR to all oligoprogressive lesions + continuation of current systemic therapy

  • Standard of care

    Other intervention

    Patients on the standard arm will be treated as per standard of care in our institution. Treatment options could include switching to next systemic therapy line, best supportive care or continuing on current systemic therapy.

Treatment groups

68 Participants
are divided into 2 treatment groups
Group A: Standard of careActive comparator 1 intervention
Group B: Experimental SABR armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

PFS

PFS defined from randomization to disease progression at any site or death

Time frame
5 years
2

OS

OS defined as time from randomization to time of death from any cause.

Time frame
5 years

Secondary outcomes

1

Quality of life Measured using the FACT-G tool, lung cancer-related patient reported outcome- CTCAE (PRO-CTCAE)

Measured using the FACT-G tool, lung cancer-related patient reported outcome- CTCAE (PRO-CTCAE)

Time frame
5 years
2

Quality of life 5-level EQ-5D (EQ-5D-5L)

questionnaire

Time frame
5 years
3

Grade ≥ 3 toxicity

Measured using the Common Terminology Criteria for Adverse Events (CTCAE v5.0)

Time frame
5 years
4

Local control

Defined as time from the end of SABR treatment to date of local failure and will be measured only in the experimental arm

Time frame
5 years

Other outcomes

Sponsors and contacts

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