TY - JOUR
T1 - Impact of a second opinion using expression and molecular analysis of FOXL2 for sex cord-stromal tumors. A study of the GINECO group & the TMRO network.
AU - Maillet, Denis
AU - Goulvent, Thibaut
AU - Rimokh, Ruth
AU - Vacher-Lavenu, Marie Cecile
AU - Pautier, Patricia
AU - Alexandre, Jerome
AU - Pujade-Laurraine, Eric
AU - Devouassoux-Shisheboran, Mojgan
AU - Treilleux, Isabelle
AU - Ray-Coquard, Isabelle
AU - Savina, Ariel
N1 - Funding Information:
Thanks to Nuchanard Chen and Carole Arbault for their technical assistance and Muriel Rogasik for editing assistance. Thanks to the French National Cancer Institute (InCa) & The French league against cancer , private donors for their financial support to ovarian cancer. Thanks also to “ L'institut Roche de Recherche et Médecine Translationnelle ”, Boulogne Billancourt, France.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Ovarian sex cord-stromal tumors (SCSTs) are rare and their diagnosis is often difficult to establish. Recently, immunostaining and molecular analysis for Forkhead box L2 (FOXL2) have been developed in this pathology. This study aims to assess the benefit of an algorithm incorporating these new tools for a better diagnosis and classification of SCSTs Seventy-two tumors with a potential diagnosis of SCSTs were addressed by 37 different pathologists to one French rare ovarian tumor expert center, member of the Rare Malignant Ovarian Tumor network (TMRO). Then a "second opinion" (SO) through an algorithm incorporating immunostaining (IHC) and molecular analysis of FOXL2 was performed for all these cases. This algorithm was then validated by all pathologists of the TMRO network. After a second opinion including molecular analysis and immunostaining for FOXL2 the initial diagnosis was changed in 15 of 72 samples (21%). FOXL2 mutation was present in 44 out of 47 adult granulosa cell tumors (94%), in 3 out of 8 Thecomas (37%), in 1 out of 10 Sertoli-Leydig cell tumors (SLSTs) (10%) and in 3 out of 5 undifferentiated-SCSTs (Und-SCSTs) (60%). Immunoexpression of FOXL2 was available in 45 cases of SCSTs: FOXL2 was expressed in 44 of them (98%). A second opinion in an expert center for all cases of SCSTs is fundamental to get an optimal classification of these rare tumors. This second opinion could be performed with an algorithm which integrates FOXL2 mutation and expression status of FOXL2 in order to standardize the practice.
AB - Ovarian sex cord-stromal tumors (SCSTs) are rare and their diagnosis is often difficult to establish. Recently, immunostaining and molecular analysis for Forkhead box L2 (FOXL2) have been developed in this pathology. This study aims to assess the benefit of an algorithm incorporating these new tools for a better diagnosis and classification of SCSTs Seventy-two tumors with a potential diagnosis of SCSTs were addressed by 37 different pathologists to one French rare ovarian tumor expert center, member of the Rare Malignant Ovarian Tumor network (TMRO). Then a "second opinion" (SO) through an algorithm incorporating immunostaining (IHC) and molecular analysis of FOXL2 was performed for all these cases. This algorithm was then validated by all pathologists of the TMRO network. After a second opinion including molecular analysis and immunostaining for FOXL2 the initial diagnosis was changed in 15 of 72 samples (21%). FOXL2 mutation was present in 44 out of 47 adult granulosa cell tumors (94%), in 3 out of 8 Thecomas (37%), in 1 out of 10 Sertoli-Leydig cell tumors (SLSTs) (10%) and in 3 out of 5 undifferentiated-SCSTs (Und-SCSTs) (60%). Immunoexpression of FOXL2 was available in 45 cases of SCSTs: FOXL2 was expressed in 44 of them (98%). A second opinion in an expert center for all cases of SCSTs is fundamental to get an optimal classification of these rare tumors. This second opinion could be performed with an algorithm which integrates FOXL2 mutation and expression status of FOXL2 in order to standardize the practice.
UR - http://www.scopus.com/inward/record.url?scp=84899408121&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2013.10.013
DO - 10.1016/j.ygyno.2013.10.013
M3 - Article
C2 - 24157616
AN - SCOPUS:84899408121
SN - 0090-8258
VL - 132
SP - 181
EP - 187
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 1
ER -