Efficacy and Safety of SBRT Combined With Becotatug Vedotin (MRG003) in EGFR-Positive Metastatic Tumor Patients With Oligometastases

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorMing-Yuan Chen

About this trial

The combination of local consolidative therapy for oligometastases with systemic therapy offers the potential for clinical cure and significantly prolongs survival in a subset of patients with advanced metastatic disease. However, a considerable proportion of patients still do not benefit from this approach.

Becotatug vedotin (MRG003) is an antibody-drug conjugate that carries the payload monomethyl auristatin E (MMAE), a microtubule inhibitor. MMAE has been shown to effectively enhance radiosensitivity in various preclinical tumor models, including head and neck squamous cell carcinoma, liver cancer, gastric cancer, pancreatic cancer, and lung cancer. Furthermore, multiple clinical studies have demonstrated the promising therapeutic potential of vicetuximab in EGFR-positive solid tumors.

Based on this background, we plan to conduct a clinical study evaluating the combination of stereotactic body radiotherapy (SBRT) for oligometastases with investigator-selected systemic therapy and Becotatug vedotin (MRG003) in patients with EGFR-positive oligometastatic tumors.

Eligibility criteria

Qualifiers

Age: 18 to 75 years (inclusive), male or female.

Patients with histologically or cytologically confirmed recurrent or metastatic solid tumors who are not amenable to curative surgery.

Oligometastatic lesions detected on imaging (biopsy of metastatic tissue is preferred but not mandatory). The total number of metastatic lesions must be <=5.

The primary tumor has been treated radically and is controlled.

Disqualifiers

History of severe hypersensitivity to any component of monoclonal antibodies.

The investigator's choice of systemic therapy regimen contains taxanes (or other microtubule inhibitors) .

Severe infection within 4 weeks prior to the start of study treatment; or active infection of CTCAE Grade>=2 requiring systemic antibiotic treatment within 2 weeks prior to the first dose.

The interval between the last dose of oral fluorouracil or small molecule targeted drugs and the first dose of study treatment is > 2 weeks or 5 half-lives (whichever is shorter);

Trial design

Treatments tested in this trial

  • Becotatug Vedotin
  • SBRT
  • Systemic Therapy/Standard of Care

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Ming-Yuan Chen

Lead sponsor

Sun Yat-sen University

Sponsor institution