CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 145 target
Drug / intervention
Systemic Therapy/Standard of Care +1 moredrug
Likely dose
Not stated in record
Key inclusion· 10
  • Metastatic disease histologically confirmed with ≤5 discrete sites amendable to SBRT
  • Metastatic breast cancer (all subtypes)
  • NSCLC without targetable mutations in EGFR, ALK, or ROS1
  • NSCLC with targetable mutations (EGFR, ALK, ROS1) with prior progression on first-line TKI
Key exclusion· 6
  • Serious medical comorbidities precluding radiotherapy
  • Pregnant or lactating women
  • Other active malignancy within last year
  • Clinical or radiological evidence of spinal cord compression

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03808337
NCT03808337Phase 2RecruitingOn TrackUpdated 4mo ago
Long Recruiting

PROMISE-005: A Phase II Randomized Study Assessing the Efficacy of Stereotactic Body Radiotherapy (SBRT) in Patients With Oligometastatic Breast or Lung Cancer

Memorial Sloan Kettering Cancer Center·interventional·Posted Jan 17, 2019·Updated Feb 27, 2026

In Brief

A Phase 2 clinical trial evaluating Stereotactic Body Radiotherapy/SBRT and Systemic Therapy/Standard of Care for Triple Negative Breast Cancer and 3 related conditions. Currently recruiting, targeting 145 participants across 12 sites.

Detailed Summary

This study is being done to determine if stereotactic body radiotherapy (SBRT) when delivered to all sites of disease in participants with 1-5 metastases will increase the length of time before participants' disease gets worse.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Recruiting
201920202021202220232024202520262027
First PostedJan 17, 2019
Enrollment StartJan 16, 2019
Primary CompletionJan 1, 2027
TodayJul 2, 2026
Enrollment to primary: 8.0 yearsPosted 7.5 years agoPrimary completion in 6 months

Interventions

Stereotactic Body Radiotherapy/SBRTradiation

Radiation to each metastatic site should be delivered to a minimum dose of 30 Gy in 5 fractions (BED of 48 Gy10). The exact dose of radiotherapy will be determined by the treating radiation oncologist. Preferred regimens for lung metastases include 50 Gy in five fractions, 48 Gy in four fractions, or 54 Gy in three fractions, although lower doses may be employed to respect dose limits to critical structures such as the esophagus. Recommended SBRT dosing for other sites includes 27 to 30 Gy in three fractions or 24 Gy in one fraction for bone metastases.

Systemic Therapy/Standard of Caredrug

Standard of care systemic therapy, including chemotherapeutics, targeted therapies, immunomodulatory agents, and hormonal therapies will be delivered at the discretion of the treating oncologist. For patients randomized to receive SBRT, systemic therapy can be continued during SBRT at the discretion and concensus of treating physicians (medical oncologist and radiation oncologist). If the treating physicians recommend discontinuing systemic therapy during SBRT, general guidelines for stopping and reinitiating systemic regimen are as follows: Hormonal therapies and immunotherapy can be continued during SBRT. Consideration can be given to holding cytotoxic chemotherapy beginning 3 to 7 days prior to the initiation of SBRT until 3 to 7 days after the completion of SBRT. Similarly, consideration can be given to holding biologic agents during SBRT and for 0 to 3 days before and after.