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Lung cancer: a novel combination of immunotherapies multiplies and prolongs the anti-tumor effect

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14 September 2024

ESMO Congress 2024

Lung cancer: a novel combination of immunotherapies multiplies and prolongs the anti-tumor effect

Could tomorrow's immunotherapies act simultaneously on several pathways of the immune system to make cancer treatments more effective? This hypothesis is supported by the results of a randomized phase 2 study which, for the first time in metastatic non-small cell lung cancers, evaluated the combination of relatlimab (an anti-LAG 3 antibody) and nivolumab (an anti-PD-1 antibody) in a 1:1 dose ratio plus platinum-doublet chemotherapy. This RELATIVITY-104 Phase 2 trial showed that the administration of two immunotherapies plus chemotherapy increased and prolonged the antitumor response.

This work is presented by Prof. Nicolas Girard, Head of the Department of Medical Oncology at Institut Curie and principal investigator of the clinical trial, during an oral presentation at the ESMO 2024 congress.

Institut Curie experts at ESMO

From September 13 to 17 in Barcelona, Spain, the world cancer community will gather for the congress of the European Society of Medical Oncology. For five days, doctors and researchers, including those from Institut Curie, will share their very promising results and their expertise to accelerate the fight against cancer on all fronts.
See following pages.

 

"While immunotherapy has already transformed the care of our patients in recent years, many avenues are being explored, particularly at Institut Curie, to relentlessly optimize these therapeutic strategies. In this sense, the positive results that we are presenting at ESMO foreshadow the immunotherapy of tomorrow and show us that we must continue this strategy of acting on several pathways to stimulate the immune system," says Prof. Nicolas Girard. "We will now launch the phase 3 study to evaluate this combination of immunotherapies in patients with a common form of metastatic lung cancer involving more than 15,000 people per year in France."

 

The leading cause of cancer-related death worldwide, with the highest mortality rates in both men and women, lung cancer affects nearly 53,000 people per year in France. The most common form is non-small cell lung cancer. Very often, this pathology is diagnosed at an advanced stage, when treatment options are limited. While primary prevention and screening of at-risk populations are crucial issues in the fight against this scourge, it is also essential to continue to develop new therapeutic strategies to treat patients in the best possible way.

 

Proof-of-concept Ph2 trial identifies potential LAG-3 responder population in metastatic NSCLC

 

Currently, the general standard treatment for metastatic non-small cell lung cancer is chemotherapy combined with immunotherapy (an antibody against the PD-1 protein, the immune system checkpoint). There were two key objectives of the randomized, proof-of-concept, RELATIVITY-104 phase 2 clinical study:

  • Investigate the clinical benefit of adding LAG-3 inhibition (relatlimab) on top of current current standard-of-care anti-PD-1 immunotherapy plus chemotherapy
  • Identify potential LAG-3 responder populations within 1L metastatic NSCLC

 

Relatlimab (anti-LAG-3 antibody) is one of the new approaches in immunotherapy. The LAG-3 receptor is expressed on the surface of certain immune cells (T cell type). It facilitates the binding between cancer cells and T lymphocytes, and prevents the anti-cancer action of the latter. In fact, by blocking the LAG-3 receptor, relatlimab can significantly improve the action of the immune system against the tumor.

 

Results pave the way for additional phase 3 investigation

 

The results presented at ESMO demonstrate not only the safety of the treatment but also nearly halving of the risk of relapse in patients who received the combination of immunotherapies plus chemotherapy (who have the PDL1 marker and non-squamous histology). There is also a benefit in terms of both objective response rates and progression free survival with the combination of nivolumab and relatlimab (1 :1 dose ratio) and chemotherapy. This phase 2 study therefore reveals a clinical benefit and provide proof of concept to initiate further Phase 3 investigation.

 

Nivolumab (NIVO) plus relatlimab with platinum-doublet chemotherapy (PDCT) vs NIVO + PDCT as first-line (1L) treatment (tx) for stage IV or recurrent NSCLC: results from the randomized phase 2 RELATIVITY-104 study. Pr Nicolas Girard. Proffered paper session NSCLC metastatic. Sous embargo jusqu’au 14 septembre, 9h, heure française.

 

OTHER MADE IN CURIE  RESULTS PRESENTED AT ESMO 2024

  • Towards progress in triple-negative breast cancer


A new clinical trial: NeoBREASTIM in progress, promoted by Institut Curie and coordinated by Dr. Emanuela Romano, medical oncologist, medical director of the Cancer Immunotherapy Center of Institut Curie will be presented at the congress.
This study aims to evaluate the combination of a new combination of immunotherapies: atezolizumab (anti-PDL1) combined with an oncolytic immunotherapy RP1 (HSV-1), as neoadjuvant therapy (i.e. before surgery), without chemotherapy, in patients with localized triple-negative breast cancer (rich in lymphocytes infiltrating the tumor). In addition, the results of a study conducted by Dr. Luc Cabel, medical oncologist at Institut Curie, on 206 Institut Curie patients with triple-negative breast cancer who received neoadjuvant chemoimmunotherapy will also be presented. This study specifies the clinical and pathological features that are associated with a complete pathological response in patients (namely the disappearance of the tumor observed at surgery).

> Poster session Breast cancer, early stage, 16 septembre : NeoBREASTIM – A Phase 2 Study of Atezolizumab plus RP1 oncolytic immunotherapy in the NeoAdjuvant setting of Triple-Negative Breast Cancer / Association between clinicopathological characteristics and pathological complete response in patients with triple negative breast cancer treated by neoadjuvant chemo-immunotherapy

 

  • Results in Ewing's sarcoma, a cancer of children and adolescents

 

Ewing sarcoma is a rare form of bone cancer that mainly affects children and young adults, with 20% of metastatic forms at diagnosis. The COMBINAIR3 study, presented at ESMO and coordinated by Dr. Valérie Laurence, medical oncologist, head of the Adolescents and Young Adults Unit at Institut Curie, evaluated a treatment strategy for patients with very high-risk Ewing sarcoma with extrapulmonary metastases, combining induction chemotherapy followed by high-dose consolidation chemotherapy with peripheral stem cell reinjection,  local treatment and then maintenance chemotherapy over two years. The results support improved recurrence-free survival rates with few serious side effects. This approach seems to be well suited to treat this rare cancer with metastases.

> Poster session Sarcoma, 14 septembre : Multimodal therapy in first line treatment of very high risk Ewing Sarcoma patients: results of the French prospective multicenter COMBINAIR3 phase II trial

 

  • An international study in favor of high-throughput sequencing in clinical routine to better personalize treatments

 

The results of the first analysis using the WAYFIND-R platform, an international registry of databases, will be presented by Prof. Christophe Le Tourneau, Head of the Early Clinical Trials Department at Institut Curie. This study, conducted on more than 2,400 patients from 24 different countries, describes the actual use of next-generation sequencing (NGS) and its impact on treatment decisions around the world. This work shows an increase in the use of targeted therapy and immunotherapy after NGS testing, in several types of cancer.


> Poster session Biomarkers & translational research, 15 septembre :
Next-generation sequencing (NGS) in routine care: Medical practice in 24 countries from the pan-cancer WAYFIND-R registry

 

  • Breast cancer: improving the prognosis of young women through better adherence to hormone therapy

 

After treatment for localized hormone-sensitive breast cancer, women receive hormone therapy for several years to limit the risk of relapse, a risk that is increased in younger women. Why is this so? One of the possible reasons is the lack of adherence to hormone therapy in this population, but no study has quantified the improvement in prognosis that could be achieved by better adherence. Using data from the French National Health Data System, Dr Elise Dumas, a post-doctoral fellow at the Ecole Polytechnique Fédérale de Lausanne (EPFL), and the Institut Curie analyzed a cohort of 121,852 patients with hormone-dependent early breast cancer (29.9% aged under 50, and 1.8% aged under 34 at diagnosis). The results of this study, presented at the ESMO annual congress, show that strict monitoring of hormone therapy could lead to a recurrence-free survival benefit of 5.6 percentage points at 5 years, in women diagnosed before the age of 34. This work underlines the need for a specific, tailored strategy for this population of young women, and resonates strongly with the research being carried out within the new Women’s Cancers Institute, an IHU co-founded by Institut Curie, Université PSL and Inserm.

 

> Mini oral session: Breast cancer, early stage - Explaining the relationships between age, endocrine therapy persistence and risk of recurrence in hormone-positive early breast cancer : A nationwide cohort study – Saturday 14 September

 

In addition to the original results presented at the congress, Institut Curie physicians and researchers are invited to various expert sessions:

 

 

 

Find the full ESMO 2024 programme online

 

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