The American Society of Clinical Oncology (ASCO) Annual Meeting is one of the leading global events in cancer research, held each year in Chicago, United States. Experts from Gustave Roussy contributed to 107 presentations featured in the 2026 programme, with a particular focus on antibody–drug conjugates (ADCs), a rapidly expanding field across new indications. At Gustave Roussy, this clinical development is supported by international translational research programmes such as OASIS and Icarus.

Focused on the clinical development of the latest advances in oncology, the ASCO Annual Meeting brings together thousands of cancer specialists from around the world to exchange on cutting-edge developments in patient care. This year in Chicago, Gustave Roussy experts contributed to a total of 107 presentations, including:
Several studies will be presented directly by physician-scientists from Gustave Roussy, including two oral presentations focused on antibody–drug conjugates, a new class of therapies showing promising clinical results by combining the efficacy of chemotherapy with the targeting precision of antibodies. By binding to a protein specifically expressed on the surface of cancer cells, these treatments deliver chemotherapy directly into the tumour while sparing healthy tissues.
Professor Yohann Loriot, Deputy Head of the Department of Drug Development and Early Phase Trials (DITEP) at Gustave Roussy, will present in an oral session the results of a phase I/II study evaluating a new treatment for women with relapsed or metastatic cervical cancer, a setting with currently limited therapeutic options. This investigational therapy, CRB-701, is an antibody–drug conjugate targeting nectin-4. It has already demonstrated encouraging activity in certain head and neck and bladder cancers
To improve the efficacy of antibody–drug conjugates and better understand resistance mechanisms in certain patients, Professor Antoine Italiano, medical oncologist and Head of the Precision Medicine Programme at Gustave Roussy, led an innovative study mapping tumours from patients with lung, bladder, gastric and endometrial cancers. Using immunohistochemistry techniques, researchers identified which proteins were expressed in each tumour, in what quantity, and with what spatial distribution. The goal is to select the most appropriate ADC for each patient based on the biological characteristics of their tumour.
Professor Fabrice André, Director of Research at Gustave Roussy, is the senior author of a study reporting the final results of the phase I/II DESTINY-Breast07 trial, presented at a clinical science symposium. This study evaluated the antibody–drug conjugate trastuzumab deruxtecan (T-DXd) as first-line therapy in combination with durvalumab, an anti–PD-L1 immunotherapy, in patients with inoperable or metastatic HER2-positive breast cancer.
T-DXd targets the HER2 protein, expressed on the surface of cancer cells in so-called HER2-positive breast cancers, which account for approximately 20% of all breast cancers. T-DXd has already demonstrated positive outcomes as a second-line treatment. Evaluating this combination in a first-line setting could redefine the standard of care and improve survival outcomes from the outset of treatment.
The OASIS project (Optimal methods to characterise ADC resistance in Solid tumours and Identify clinically useful biomarkerS) is a European research programme dedicated to optimising ADC therapies. These innovative treatments precisely target cancer cells, thereby reducing damage to healthy tissues. Coordinated by Gustave Roussy and led by Dr Barbara Pistilli, the project aims to develop tools enabling clinicians to select the most appropriate ADC for each patient, considering both clinical characteristics and tumour biology.
Professor Sophie Postel-Vinay, medical oncologist and physician-scientist within Gustave Roussy’s DITEP, will present the latest advances on an innovative strategy: exploiting tumour genetic vulnerabilities to improve targeting. Around 15% of all cancers, including lung, brain, pancreatic tumours, mesotheliomas, and certain lymphomas, exhibit loss of the MTAP gene. This alteration creates a metabolic imbalance in tumour cells, making them dependent on another enzyme, PRMT5, for survival. This dependency is precisely what new treatments aim to exploit: by inhibiting PRMT5, tumour cells can be weakened while sparing healthy tissues.
A new generation of drugs, more targeted and better tolerated than earlier compounds, is currently being investigated in more than 65 clinical trials worldwide. Professor Postel-Vinay will present available results and explore combination strategies with other anticancer therapies. Long confined to PARP inhibitors, this synthetic lethality approach is now expanding to new targets, offering promising prospects for patients with often limited treatment options.
Early-phase trials are essential in oncology. Without them, no new treatment could reach the market. They represent the first stages in the life of a drug once it leaves the laboratory. These phase I or I/II trials aim to administer new anticancer therapies in humans for the first time, to assess initial signs of anti-tumour activity, evaluate safety and toxicity profiles, and determine the appropriate dose, schedule, and duration of treatment.
Gustave Roussy is the leading European centre for early-phase clinical trials, through its Department of Drug Development and Early Phase Trials (DITEP).
Of the 516 therapeutic trials conducted at the Institute in 2025, one-third were early-phase studies.
In parallel, Gustave Roussy experts will present five studies in rapid oral sessions, including two focused on therapeutic vaccines: