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Clinical Trial Summary

Immune checkpoint inhibitors (ICIs), such as anti-PD-1/PD-L1 agents, initially evaluated in advanced non-curative pathologies, are now being evaluated in adjuvant or even neoadjuvant curative treatment conditions. This paradigm shift is leading to the treatment of young women, particularly in the context of gestational trophoblastic tumours. Given the potential autoimmune side-effects affecting endocrine functions, as well as their impact on maternal-foetal tolerance mechanisms, accurate assessment of post-ICT fertility is necessary. In the coming years, treatment with anti-PD-L1 (avelumab) could become a cornerstone of the therapeutic strategy for patients with gestational trophoblastic tumours. However, these patients are often young and of childbearing age, so safety of use in terms of fertility and successful pregnancies is an essential factor in the widespread use of immunotherapy as a treatment option. Some studies have reported the possibility of conceiving after avelumab treatment, but no cohort has been reported. This study aims to explore fertility and the course of potential pregnancy in 50 patients treated with anti-PD-L1 (avelumab) over the last 5 years in several French centres.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06242522
Study type Interventional
Source Hospices Civils de Lyon
Contact Pierre-Adrein BOLZE, ¨Pr
Phone 04 78 86 66 78
Email pierre-adrien.bolze@chu-lyon.fr
Status Not yet recruiting
Phase N/A
Start date April 1, 2024
Completion date April 1, 2025

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