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Author Spotlight: Advancing Personalized Medicine in Ovarian Cancer
Published on: February 23, 2024
[Optimal tissue quantity for molecular ancillary studies in multicenter clinical trials in gynecological oncology:
Alexis Trecourt1, Guillaume Bataillon2, Isabelle Treilleux3
1Service de pathologie multi-sites, hospices civils de Lyon, centre hospitalier Lyon Sud, 69310 Pierre-Bénite, France; Centre pour l'innovation en cancérologie de Lyon (CICLY), UR3738, faculté de médecine et de Maïeutique de Lyon Sud-Charles-Mérieux, université Claude-Bernard Lyon 1, 69921 Oullins, France; ARCAGY-GINECO Association de loi 1901, promoteur d'études cliniques, 8, rue Lamennais, 75008 Paris, France.
Abstract:
The national investigators group for ovarian and breast cancer studies (GINECO) is an academic clinical research group specialized in gynecological oncology. Within the translational research group, the pathologists have several roles, including qualifying samples from patients included in clinical trials (tumor surface and cellularity). Since 2015, several clinical trials have required the qualification of tissue material, leading to a substantial database gathering tumor surface and cellularity associated with the concentration and quantity of DNA/RNA extracted. The main objective of this study was to investigate variations in nucleic acid concentration and quantity depending on the tumor cellularity and surface, using 1734 formalin-fixed, paraffin-embedded (FFPE) specimens from several GINECO clinical trials. The quantities of DNA and RNA extracted appeared to correlate well with tumor surface. The amount of RNA extracted also appeared to correlate with tumor cellularity. An optimal DNA concentration (>50ng/μL) was achieved with a tumor surface of at least 51-100mm2 and a tumor cellularity of at least 20%. An optimal RNA concentration (>100ng/μL) was obtained with a tumor surface of at least 26-50mm2 and a tumor cellularity of at least 51%. These data underline the importance of sending FFPE material with the highest tumor surface and cellularity when including patients in clinical trials. Inclusion in clinical trials enables patients to benefit from innovative therapeutic management.

