Addition of Hypofractionated High Dose Radiation in Oligometastatic Disease

NCT06141070 | Recruiting Phase 3

• 1 other identifier: The ANDROMEDA trial
• Study Type: interventional
• Target: 240
• Locations: 1 country
• Sites: 6

Brief Summary

This is a 2:1 randomized multicentre open label phase III study of radiation combined with standard systemic treatment compared with systemic treatment alone in oligometastatic (≤5 metastases) NSCLC. Stratification factors: performance status, gender and systemic strategy. The systemic treatment consists of chemotherapy/chemoimmunotherapy or immunotherapy and is given according to local practice. During the first 3 months of systemic treatment, aiming to start around the 2nd cycle is radiotherapy delivered to all known lesions. Preferably with SBRT /SRT/SRS but conventional radiotherapy may also be used. After the first three cycles of systemic treatment, the patients are assessed, and after four cycles, they are continuing maintenance therapy if indicated. The patients are followed with radiology every three months.

Conditions

Non Small Cell Lung Cancer

Outcome Measures

Primary Outcomes (1)

• Overall survival (OS)

  Time to death

  From date of randomization until the date of death from any cause, whichever came first, assessed up to 60 months

Secondary Outcomes (2)

• Progression-free survival (PFS)

  From date of randomization until the date of first documented systemic progression or date of death from any cause, whichever came first, assessed up to 60 months

• Local control (LC)

  At 12 months after randomization

Study Arms (2)

A, standard systemic therapy

ACTIVE COMPARATOR

Standard systemic chemoimmunotherapy

Drug: Standard systemic therapy

B, Radiotherapy + systemic therapy

EXPERIMENTAL

Standard systemic chemoimmunotherapy and radiation to all known lesions

Other: Standard systemic therapy + radiotherapy

Interventions

Standard systemic therapy + radiotherapy OTHER

Combined systemic therapy + radiation

B, Radiotherapy + systemic therapy

Standard systemic therapy DRUG

Chemoimmunotherapy or immunotherapy

A, standard systemic therapy

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent obtained from the subject prior to performing any protocol- related procedures, including screening procedures
• Histological or cytological diagnosis of NSCLC
• Stage IV disease with ≤5 metastases (not including primary tumour or mediastinal nodes, N1-N3)
• Patient deemed fit for first line chemoimmunotherapy, immunotherapy or chemotherapy
• Extra-thoracic metastases accessible for stereotactic body radiotherapy (SBRT)
• Thoracic tumour(s) accessible for SBRT or conventional radiotherapy
• Received no prior systemic treatment or radiation therapy for NSCLC (previous adjuvant systemic therapy is allowed)
• Age \> 18 years at time of study entry, no upper age limit
• WHO performance status 0-2
• Adequate normal organ and marrow function Evidence of post-menopausal status or negative urinary or serum pregnancy test for female pre-menopausal subjects.
• Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up

You may not qualify if:

• Solitary brain lesion or contralateral lung lesion as the only distant metastasis
• Participation in another clinical study with an investigational product during the last 4 weeks
• Patients with EGFR+, ALK+, ROS1+ disease or any other genetic alteration that would result in a TKI based first line treatment (i.e. first line treatment not being chemoimmuno- or immunotherapy)
• Malignant pleural fluid, or ascites (malignant cells or clinical judgement) or excessive fluid hampering radiation according to protocol
• Leptomeningeal disease
• Pulmonary fibrosis making protocol stipulated treatment hazardous (low grade radiologic findings are allowed as assessed by the investigator)
• Not deemed fit for standard first line systemic therapy
• Second primary residual malignancy. Other malignancy diagnosed and treated \> 2 years ago without relapse and deemed to have a low likelihood of relapse is allowed. (Carcinoma in situ of the cervix or adequately treated basal cell carcinoma of the skin \< 2 years are allowed, as is other low-grade malignancy with low likelihood of becoming metastatic or impact on survival e.g. low-grade prostate cancer not in need of treatment)
• Female subjects who are pregnant or breastfeeding or male or female subjects of reproductive potential who are not willing to employ effective birth control from screening to 90 days after the last dose of systemic therapy
• Any condition that, in the opinion of the investigator, would interfere with evaluation of study treatment or interpretation of patient safety or study results

Sponsors & Collaborators

• Vastra Gotaland Region: lead

Study Sites (6)

Dept of Oncology

Gothenburg, 41345, Sweden

RECRUITING

Dept of pulmonary medicine

Linköping, Sweden

NOT YET RECRUITING

Dept of pulmonary medicine

Lund, Sweden

NOT YET RECRUITING

Dept of Oncology

Stockholm, Sweden

RECRUITING

Dept. of Oncology

Umeå, Sweden

RECRUITING

Dept. of Oncology

Uppsala, Sweden

RECRUITING

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell Lung

Interventions

Radiotherapy

Condition Hierarchy (Ancestors)

Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Respiratory Tract Neoplasms; Thoracic Neoplasms; Neoplasms by Site; Neoplasms; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Therapeutics

Central Study Contacts

Andreas Hallqvist

CONTACT

+46313427954; andreas.hallqvist@vgregion.se

Marielle Drousiotis

CONTACT

+46313424509; marielle.drousiotis@vgregion.se

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER GOV
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 13, 2023
• First Posted: November 21, 2023
• Study Start: December 1, 2023
• Primary Completion (Estimated): December 1, 2028
• Study Completion (Estimated): December 1, 2028
• Last Updated: April 14, 2026

Record last verified: 2026-04

Locations

SE (6)