ANTELOPERecruiting

Comparison of pemetrexed-free immunochemotherapy (atezolizumab/carboplatin/nab-paclitaxel) with standard immunochemotherapy (pembrolizumab/platinum/pemetrexed) in people with metastatic lung cancer (TTF-1 negative)

Gender
Women and men
Age
18 years and older
Trial type
Interventional
Line of therapy
First line
Phase
Phase II

What is this trial about?

The standard treatment for people with newly diagnosed metastatic lung adenocarcinoma is immunochemotherapy, which often includes the active ingredient pemetrexed. However, there is evidence that this drug is not very effective in patients with certain cancer characteristics. The goal of the ANTELOPE study is to investigate whether pemetrexed-free immunochemotherapy is more effective in these patients than the standard pemetrexed-containing therapy. Women and men aged 18 and older who have been newly diagnosed with lung cancer exhibiting specific characteristics (metastatic, TTF-1-negative, PD-L1 < 50%) and who have not yet received systemic treatment are eligible to participate in this study.

Trial flow

Requirements

Diagnosis: Lungcancer

Age: 18 years and older

Line of therapy: Erstlinie / bisher keine Therapie

Key inclusion criteria: TTF1-negative, metastatic; non-squamous NSCLC; PD-L1 < 50%

Allocation

Randomisierung

Treatment

Atezolizumab, Carboplatin and Nab-Paclitaxel Administered for 4 cycles with subsequent maintenance with atezolizumab monotherapy until loss of clinical benefit or occurrence of unacceptable toxicity
Pembrolizumab, Platinum and PemetrexedAdministered for 4 cycles with subsequent maintenance with pembrolizumab AND pemetrexed until loss of clinical benefit or occurrence of unacceptable toxicity

Follow-up

30 months

Detailed description

Non-small cell lung cancer (NSCLC) is the most common form of lung cancer, which also includes lung adenocarcinoma. It develops when certain cells in the lung multiply uncontrollably. “Non-small cell” means that the cancer cells appear larger under a microscope than those in the rarer form, small cell lung cancer. An “adenocarcinoma” originates from glandular cells that produce mucus, usually in the outer regions of the lung. This disease usually grows more slowly than small-cell lung cancer and, depending on the stage, can be treated with surgery, radiation, medication, or a combination of these. The specific treatment that is appropriate depends on how far the cancer has progressed and whether certain changes (mutations) are present in the tumor cells. In most of these tumors, a specific protein, “Thyroid Transcription Factor 1” (TTF-1), can be detected.

Metastasis means that cancer cells break away from the original tumor, travel through the bloodstream or lymphatic system, and form new tumors in other parts of the body. These are called metastases (secondary tumors). Once the cancer has formed metastases, surgery is usually no longer sufficient because the disease has spread throughout the body. Treatment then aims to slow the growth of the cancer, alleviate symptoms, and maintain quality of life. The standard first-line treatment for metastatic lung cancer is a combination of immunotherapy (so-called checkpoint inhibitors) and chemotherapy. This standard therapy often includes the chemotherapy drug pemetrexed. However, clinical evidence suggests that patients whose tumors do not produce TTF-1 (TTF-1-negative) may respond better to treatment without pemetrexed. Checkpoint inhibitors are drugs that reactivate the immune system so that it can better fight cancer cells.

The goal of the ANTELOPE study is therefore to evaluate the effectiveness of pemetrexed-free therapy in a direct comparison with standard therapy that includes pemetrexed. The most important outcome measure is overall survival. Participants in the study will be randomly assigned to two groups. Group A will receive the pemetrexed-free treatment: atezolizumab (immunotherapy), carboplatin (chemotherapy), and nab-paclitaxel (chemotherapy). Group B will receive the standard treatment containing pemetrexed: pembrolizumab (immunotherapy), cisplatin or carboplatin (chemotherapy), and pemetrexed (chemotherapy). The study is open-label, meaning it is not blinded; that is, medical staff and participants know which medications are being administered.

Eligible participants are women and men aged 18 and older who have been newly diagnosed with lung cancer exhibiting specific characteristics (metastatic, TTF-1-negative, PD-L1 < 50%). They must not have received any prior systemic treatment.

Facts

  1. What condition: Lung cancer
  2. Cancer characteristics: metastatic; non-small cell lung cancer (NSCLC, non-squamous); TTF-1 negative; untreated (first-line); no EGFR/ALK mutations; PD-L1 < 50%
  3. What the study investigates: The efficacy of pemetrexed-free immunochemotherapy (Arm A) versus standard pemetrexed-containing immunochemotherapy (Arm B)
  4. Study objective: To determine whether pemetrexed-free therapy leads to longer overall survival than standard therapy
  5. How long will the study last: The follow-up period for the primary endpoint is 30 months
  6. Study characteristics: Phase 4 study, randomized, comparative, open-label (unblinded)

Trial sites

44 trial sites in Germany are listed. Find a site near you.

  • Klinikum St. Marien Amberg

    Mariahilfbergweg 7, 92224 Amberg

    Active, not recruiting
  • Universitätsklinikum Augsburg

    Stenglinstraße 2, 86156 Augsburg

    Recruiting
  • Hochtaunus-Kliniken

    Zeppelinstrasse 24, 61352 Bad Homburg

    Status unknown
  • Medizinisches Versorgungszentrum Taunus GmbH

    61352 Bad Homburg

    Status unknown
  • Charité – Universitätsmedizin Berlin

    Berlin

    Active, not recruiting
  • Evangelische Lungenklinik Berlin

    Lindenberger Weg 27, 13125 Berlin

    Status unknown

This list is compiled to the best of our knowledge but without guarantee: it may be incomplete, and a site's recruitment status can change at any time.

Medical editorial team

  • Dr. med. Sebastian SommerSpecialist in internal medicine with a focus on hematology and oncology
  • PD Dr. med. Matthias FröhlichSpecialist in internal medicine, immunology and emergency medicine

This description is based on the public trial registry (NCT05689671) and was translated into plain language by our medical editorial team. Whether participation is an option for you is a decision you make together with your treating physician.