Immunotherapy Without Chemotherapy for Advanced Lung Cancer Patients With High PD-L1 Levels

Traditionally, anticancer drug development has been guided by tumor histology and largely focused on tissue-specific characteristics rather than the underlying biological mechanisms driving disease progression. Conventional anticancer therapies, which are often nonspecific, are associated with substantial toxicity and adverse events, and their efficacy frequently diminishes over time due to the emergence of drug resistance. These limitations have driven a paradigm shift toward the development of therapies that target the molecular and biological features of cancer rather than its anatomical origin.

Advances in tumor biology and immunology have profoundly transformed the oncology treatment landscape. Once considered speculative, biomarker-driven and tissue-agnostic therapeutic approaches are now supported by robust clinical evidence. Since 2017, regulatory approvals have validated this shift, beginning with the FDA approval of pembrolizumab for tumors characterized by high microsatellite instability (MSI-H), followed by additional tumor-agnostic agents. To date, seven therapies have received FDA approval for tissue-agnostic indications, underscoring the clinical relevance of shared biological features across cancer types.

A comprehensive understanding of drug mechanisms of action, together with an in-depth assessment of the tumor microenvironment and its inflammatory status, has emerged as a critical determinant of treatment efficacy, particularly in patients who fail to respond to conventional therapies. The increasing focus on immune-tumor interactions has led to the identification of key immune regulatory pathways that represent attractive targets for tumor-agnostic drug development. Among these, CD8⁺ T-cell immunophenotypes play a central role in mediating responses to immunotherapy. Unlike classical oncogenic driver alterations, immune checkpoint molecules such as PD-1 and PD-L1 are not mutated in PD-L1-positive tumors. Nevertheless, PD-L1 expression has been observed across multiple cancer types with otherwise unrelated genomic alterations, making the PD-1/PD-L1 axis a prototypical tumor-agnostic therapeutic target. Pharmacological blockade of this pathway using monoclonal antibodies can restore antitumor T-cell activity and induce meaningful clinical responses.

Anti-PD-1 monotherapy has demonstrated substantial clinical benefit in advanced or metastatic non-small cell lung cancer (NSCLC) with high PD-L1 expression (tumor proportion score [TPS] >50%) across multiple randomized clinical trials. In the KEYNOTE-024 study, pembrolizumab significantly improved objective response rate (ORR) and overall survival (OS) compared with platinum-based chemotherapy. At a median follow-up of 24 months, median OS was 26.3 months for pembrolizumab versus 13.4 months for chemotherapy, with a hazard ratio of 0.62. Notably, the estimated 5-year OS rate was 31.9% in the pembrolizumab arm compared with 16.3% in the chemotherapy arm, highlighting the potential for long-term disease control with immunotherapy.

Similarly, the EMPOWER-Lung 1 trial demonstrated the superiority of cemiplimab over chemotherapy in patients with PD-L1 TPS ≥50%. Median OS was not reached in the cemiplimab arm versus 14.2 months with chemotherapy, and progression-free survival (PFS) was significantly prolonged. Importantly, these benefits were observed despite a high crossover rate, reinforcing the robustness of the survival advantage conferred by PD-1 blockade.

The KEYNOTE-042 study further extended these findings by demonstrating an overall survival benefit for pembrolizumab across PD-L1 TPS subgroups (≥50%, ≥20%, and ≥1%). These results supported the extension of pembrolizumab monotherapy as a first-line option for patients with locally advanced or metastatic NSCLC lacking EGFR or ALK alterations, including those with lower PD-L1 expression levels.

Collectively, these data led to FDA and EMA approvals of anti-PD-1 antibodies, including pembrolizumab and cemiplimab, as first-line monotherapy for advanced or metastatic NSCLC with PD-L1 TPS >50%, as assessed by companion diagnostic immunohistochemistry assays. However, emerging clinical evidence has identified a subset of patients who experience paradoxical hyperprogressive disease (HPD) following initiation of anti-PD-1 monotherapy. HPD is characterized by rapid acceleration of tumor growth and is associated with early mortality. This phenomenon likely explains the early crossover of survival curves observed in trials comparing immunotherapy monotherapy with chemotherapy.

In contrast, such early survival crossover is not observed in studies comparing chemotherapy alone with chemotherapy-immunotherapy combinations, including CheckMate-227, CheckMate-9LA, KEYNOTE-189, and KEYNOTE-407. As a result, many thoracic oncologists, particularly in France, have adopted chemo-immunotherapy combinations as first-line treatment for PD-L1-high NSCLC, as these regimens increase ORR and reduce the risk of hyperprogression. However, this approach exposes patients who would otherwise benefit from anti-PD-1 monotherapy-estimated at approximately 40% of PD-L1-high NSCLC cases-to unnecessary chemotherapy-related toxicity, potentially compromising long-term survival and quality of life.

Supporting this concern, a recent systematic review and reconstructed individual patient data analysis examined the impact of platinum-based chemotherapy (PCT) combined with immune checkpoint inhibitors in metastatic NSCLC. This analysis demonstrated that PCT-containing regimens were associated with a higher risk of acquired resistance at 12 months and a shorter median duration of response compared with PCT-free immunotherapy combinations. In contrast, the addition of CTLA-4 inhibitors did not significantly increase resistance rates. These findings suggest that while chemotherapy may enhance early disease control, it may also accelerate the development of resistance to immune checkpoint blockade.

Taken together, these observations emphasize the urgent need to refine patient selection and optimize treatment sequencing in NSCLC immunotherapy. Multiple early-phase studies have independently identified soluble plasma biomarkers with predictive value for anti-PD-1 monotherapy efficacy. Building on this work, translational analyses conducted at Gustave Roussy Cancer Center identified a composite signature of circulating soluble biomarkers-including interleukin-6 (IL-6), interleukin-8 (IL-8), soluble CD14 (sCD14), soluble CD25 (sCD25), and growth differentiation factor-15 (GDF-15). This Pro-Tumoral Inflammation (PTI) signature is strongly associated with primary resistance to anti-PD-1 therapy and provides a biologically grounded framework for improving patient stratification and therapeutic decision-making in advanced NSCLC. depending on their PTI score, some patients could be identified early on as being at higher risk of non-response (including hyperprogression) under anti-PD1 monotherapy.

Here the investigators aim to implement those biomarkers in an exploratory sub-protocol of the METAREM master protocol for a prospective validation of their value to stratify NSCLC patient's care.

Thus, META-1 trial aims to incorporate PTI score as a biomarker for patient selection via baseline PORTRAIT profile. In the REMISSION program, which includes METAREM master protocol and its sub-protocols, the Meso Scale Discovery multiplex ultrasensitive titration platform will be used to titrate the cytokine levels in plasma from NSCLC patients which will permit to establish the PTI score for patient selection.

META-1 is a prospective, French, multicentric, phase II, sub-protocol of the METAREM master protocol. META-1 focuses on evaluating the value of the PTI score to identify patients who could benefit from the long-term efficacy an anti-PD1 monotherapy, while avoiding the risk of hyperprogression and the toxicities of chemotherapy. Using ultrasensitive methods, the patient's plasma samples (collected for baseline PORTRAIT) will be rapidly analysed. Based on PTI score cut-off levels i.e., patients with PTI=0, the patient will be selected for inclusion in the META-1 trial.

Designed as an academic proof-of-concept study, META-1 aims to validate the hypothesis that can enable personalized benefit-risk predictions, helping identify the most advantageous treatment for advanced NSCLC patients.

Of note, both anti-PD1 monotherapy and anti-PD1 in combination with carboplatin doublet chemotherapies are currently standard of care options as first-line treatment for advanced NSCLC with PD-L1 TPS > 50%. The choice of one or the other treatment option currently relies on the sole practitioner choice without objective decision criteria.

Trial aim to demonstrate that blood titration of the PTI score can help to orient patients to one or the other treatment option with a biological rationale and an objective titration of soluble blood factors.

META-1 trial involves the following key steps:

Patient selection will be based on the eligibility and inclusion criteria of the METAREM master protocol and the META-1 trial. Only patients who have consented to both the master protocol and the trial are eligible to be included in the META-1 trial. Along with the PORTRAIT immune profile, inclusion criteria are also based on pathology, imaging, clinical setting, and routine biological criteria.

Patients with tumors having a PD-L1 TPS > 50% according to approved CDx IHC assays (using the anti-PD-L1 IHC staining clones 22C3, 28-8 and SP263)11 will be tested at baseline within the PORTRAIT immune profiling.

Fresh blood samples will be mandatory for PORTRAIT analysis prior to inclusion in the META-1 trial, while fresh tumor samples will be optional according to the following scenarios:

1. if patients have already undergone their diagnostic tumor biopsy to establish their PD-L1 IHC score before signing the METAREM master protocol consent, a new baseline PORTRAIT tumor biopsy will be optional. Archived diagnostic tumor samples may be used.
2. if patients provide consent for the METAREM prior to their initial diagnostic tumor biopsy, the baseline PORTRAIT analysis may be performed on that fresh tumor biopsy.
3. A minimum of 10 FFPE blank slides should be made available at baseline either from a previous tumor biopsy or a new one performed during the METAREM screening period. If no baseline tumor material is available and a new tumor biopsy cannot be performed, the investigator must request an exemption from the tumor biopsy requirement from both the sponsor and the coordinating investigator of the META-1 trial.
4. Patients with PTI score = zero - low levels of IL6, IL8, sCD14, sCD25 and GDF15 - will be eligible to participate in the META-1 trial and receive anti-PD1 monotherapy (pembrolizumab or cemiplimab) according to the approved and reimbursed standard of care (SoC) in France. Once enrolled into the META-1 trial, patients will be treated with an anti-PD1 monotherapy per standard of care (pembrolizumab or cemiplimab) until disease progression, unacceptable toxicity, death, investigator's decision, or patient's decision. For patients whose initial baseline tumor biopsy for PORTRAIT has been collected, an on-treatment PORTRAIT analysis will be repeated at C2D1 (W3) for immune profiling. As with the baseline biopsy, the on-treatment tumor biopsy will not be mandatory, as patients will be treated according to the standard of care. RECIST v1.1 imaging assessment should be performed by the investigator at the screening visit (baseline PORTRAIT), the inclusion visit, C3D1 (W6) and C5D1 (W12) according to the SoC. After 12 weeks of treatment, subsequent RECIST v1.1 imaging assessment should be performed by the investigator as per the SoC schedule and local site practices during treatment and follow-up period, until documented disease progression or death, whichever occurs first, for a maximum follow-up period of 36 months.
5. Patients with PTI score ≥ 1 - high levels of IL6, IL8, sCD14, sCD25 and GDF15 - will be followed for up to 36 months according to the SoC to assess disease progression and overall survival, provided they have given their consent. Throughout the study, radiological examinations and tumor assessments by the investigator will be performed in accordance with the SoC. Patients will receive standard treatment at the discretion of the treating physician. Information on treatments and any newly initiated therapies will also be collected. These patients will not undergo any sampling during the META-1 trial, except for samples collected during the screening visit conducted under the METAREM master protocol.