Phase III Randomized Controlled Trial Comparing Maintenance Systemic Therapy Alone With Systemic Therapy Plus Local Ablative Treatment for Patients With Advanced Stage IV Non-small Cell Lung Cancer

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Radiation, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Unfortunately, most patients are already at a very advanced stage when they are diagnosed with lung cancer, i.e. the cancer has already spread outside the lungs forming metastases. The current standard of care therapy at this advanced stage of lung cancer includes systemic anti-cancer therapy such as chemotherapy, immunotherapy to boost the body's immune response, or targeted therapy that directly hinders tumor growth. In this study, the aim is to find out whether it is better if, after a good response to the standard therapy, the remains of main tumor and the metastases are additionally treated by surgery and/or radiation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Patients fulfilling all of the following inclusion criteria at screening may be enrolled in the trial.

• The inclusion criteria are irrespective from the tumor burden at the time of primary diagnosis before initiation of first line systemic therapy. Neurosurgical diagnostic resection of one single CNS metastasis or laparoscopic resection of one adrenal metastasis before trial inclusion is allowed.

• Adults (18 years or older)

• Tissue confirmed, pre-treatment clinical stage IV NSCLC

• ECOG performance status ≤ 1

• Patients responding after 3 cycles (4th bridging cycle up until randomization is allowed) or 3 months of first line SoC systemic therapy with PR or SD in restaging imaging, and presenting with (induced) oligometastatic or oligopersistent NSCLC defined as a maximum of 5 residual extracranial, distant metastases

• Patients may have up to 5 cranial metastases in addition to the oligoresidual extracranial metastases as long as they are amenable for radiotherapy or surgery.

• The primary tumor and all oligopersistent metastases must be amenable for radical LAT (surgery or radiotherapy)

• Patients of reproductive age agree to use double contraception during the study

• Patient is able to understand trial procedures and is able/willing to adhere to trial procedures as confirmed by signature

Locations
Other Locations
Switzerland
Kantonspital Aarau
RECRUITING
Aarau
IOSI Ospedale Regionale di Bellinzona e Valli
RECRUITING
Bellinzona
Kantonsspital Graubuenden
RECRUITING
Chur
Hôpital Fribourgeois - Hôpital Cantonal
RECRUITING
Fribourg
Hôpitaux Universitaires Genève HUG
RECRUITING
Geneva
Luzerner Kantonsspital
RECRUITING
Lucerne
Universitätsspital Zürich
RECRUITING
Zurich
Contact Information
Primary
Gwendoline Wicki
trials@sakk.ch
+41 31 389 91 91
Time Frame
Start Date: 2023-12-21
Estimated Completion Date: 2027-11-01
Participants
Target number of participants: 128
Treatments
Experimental: Intervention group: Local consolidative treatment (LAT) & Systemic Therapy
All patients undergo standard of care (SoC) first-line systemic therapy according to the results of the molecular analysis obtained from the diagnostic biopsy, as per standard of the respective center.~Patients will undergo additional complete surgical resection of the primary tumor with mediastinal lymph node sampling or radical radiotherapy (preferred stereotactic body radiotherapy (SBRT) to the primary tumor. Surgery and/or SBRT to the metastases will be performed before or after the treatment of the primary tumor according to the clinical need. Thereafter, the treatment will be followed by systemic anticancer treatment as SoC.
Active_comparator: Control group: Systemic Therapy
Patients of the control group will receive systemic anticancer treatment alone chemotherapy, chemo-immunotherapy, immunotherapy alone, or targeted treatment).
Sponsors
Leads: Swiss Cancer Institute

This content was sourced from clinicaltrials.gov

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