About this trial
Primary objective of this study is to identify and describe the clinico-biological and molecular characteristics of tumors with somatic POLE (Polymerase ɛ)/POLD1 mutation identified by molecular biology platforms for all stages and primary sites combined
Eligibility criteria
Qualifiers
Any tumor presenting a variant of the exonuclease domain of POLE (exons 9 to 14) classified as pathogenic by the project working group, including: the 4 hotspots of mutations described (codons 286 (P286R/H/L), 411 (V411L), 459 (S459F), 424 (L424/V/I), (2).
Any tumor presenting a variant of the exonuclease domain of PolD1 (exons 8-12), classified as pathogenic by the project working group, including : C319Y(10).
Disqualifiers
Tumor without POLE or POLD1 mutation
Tumor with POLE mutation identified in research studies retrospective research
Opposition of the patient to the registration of his data in the cohort
Trial design
Treatments tested in this trial
- Not listed