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Search / Trial NCT04339218

Cryoablation in Combination (or Not) With Pembrolizumab and Pemetrexed-carboplatin in 1st-line Treatment for Patients With Metastatic Lung Adenocarcinoma

Launched by INSTITUT BERGONIÉ · Apr 6, 2020

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Lung Adenocarcinoma, Immunotherapy, Cryoablation

ClinConnect Summary

This clinical trial is investigating whether combining a treatment called cryoablation with two other medications, pembrolizumab and pemetrexed-carboplatin, can help patients with metastatic lung adenocarcinoma live longer. In this study, participants will be randomly assigned to one of two groups: one group will receive cryoablation along with the medications, while the other group will only receive the medications. Cryoablation is a procedure that freezes cancer cells to help shrink tumors. The trial aims to see if this combination leads to better survival rates after one year compared to the standard treatment.

To be eligible for this study, patients must have a confirmed diagnosis of lung adenocarcinoma that has spread to other parts of the body, and they should be at least 18 years old. Participants need to have two measurable tumors, one of which can be treated with cryoablation. This study is currently recruiting participants, and those who join can expect to follow a specific treatment plan and attend regular check-ups. It’s important to note that patients with certain other health conditions or who have had specific treatments in the past may not be eligible.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Histologically or cytologically confirmed non-small lung adenocarcinoma.
  • 2. Metastatic disease.
  • 3. Treatment with pembrolizumab in combination with pemetrexed-carboplatin as per market authorization.
  • 4. At least two target lesions (RECIST1.1), measurable with CT or MRI :
  • 1. One target lesion that is amenable for accurate repeated measurements,
  • 2. One target lesion (15-40 mm) that is amenable for cryoablation treatment including lung, kidney, adrenal, soft tissue and lytic bone lesions. Liver and sclerotic bone lesions are not allowed to be treated by cryoablation.
  • 5. Age ≥ 18.
  • 6. Performance status ≤ 2.
  • 7. Women of childbearing potential must have a negative serum pregnancy test prior to registration.
  • 8. Recovery to grade ≤ 1 from any adverse event derived from previous treatment (excluding alopecia)
  • 9. Patients with a social security in compliance with the French law (Loi Jardé).
  • 10. Patients must be willing and able to comply with scheduled visits, treatment plan, laboratory tests and other study procedures.
  • 11. Voluntarily signed and dated written informed consents prior to any study specific procedure.
  • Exclusion Criteria:
  • 1. Squamous cell tumors and other than adenocarcinoma.
  • 2. Prior systemic treatment for advanced non-small cell lung cancer (except adjuvant therapy after complete resection).
  • 3. Current or prior use of immunosuppressive medication including any use of oral glucocorticoids, within 21 days before the first dose of pembrolizumab.
  • 4. Known contra-indication and/or hypersensitivity to PD1/PD-L1 antagonist and/or cytotoxic therapy.
  • 5. Known contra-indication to cryoablation.
  • 6. Abnormal coagulation contraindicating biopsy.
  • 7. Prior or concurrent malignant disease diagnosed or treated in the last 2 years except for adequately treated in situ carcinoma of the cervix, basal or squamous skin cell carcinoma or incidentally discovered good prognosis prostate cancer (T stage \< pT3 and Gleason ≤ 7).
  • 8. Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy.
  • 9. Subjects who participated in an investigational drug or device study within 28 days prior to study entry.
  • 10. Known infection with HIV, hepatitis B, or hepatitis C.
  • 11. Females who are pregnant or breast-feeding.
  • 12. Men or women refusing contraception.
  • 13. Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study.
  • 14. Previous enrolment in the present study.
  • 15. Individuals deprived of liberty or placed under legal guardianship.

About Institut Bergonié

Institut Bergonié is a leading cancer research and treatment center based in Bordeaux, France, renowned for its commitment to advancing oncology through innovative clinical trials and cutting-edge therapies. As a prominent sponsor of clinical research, the institute focuses on improving patient outcomes and quality of life by integrating multidisciplinary approaches in cancer care. With a strong emphasis on collaboration and translational research, Institut Bergonié actively engages in partnerships with academic institutions, industry leaders, and healthcare organizations to foster advancements in cancer treatment and enhance the understanding of malignancies. Its dedication to excellence in patient care and research positions Institut Bergonié at the forefront of the fight against cancer.

Locations

Bordeaux, Gironde, France

Patients applied

0 patients applied

Trial Officials

Jean PALUSSIERE, MD

Principal Investigator

Institut Bergonié

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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