TY - JOUR
T1 - Clinicopathological analysis of mixed endometrial carcinomas: clinical relevance of different neoplastic components
AU - Rossi, Esther Diana
AU - Bizzarro, Tommaso
AU - Monterossi, Giorgia
AU - Inzani, Frediano
AU - Fanfani, Francesco
AU - Scambia, Giovanni
AU - Zannoni, Gian Franco
PY - 2017
Y1 - 2017
N2 - Mixed endometrial carcinomas (MECs) refer to tumors characterized by 2 or more distinct histotypes mostly that comprised endometrioid (EC) and serous/clear cell carcinomas (SC/CC). The specific quantification of these distinct components represents a challenging and critical point for both prognosis and management. Herein, we analyze a large series of MEC and compare them with EC and SC/CC. We evaluated a series of 69 MECs between January 2002 and December 2015. We compared the MEC series with 186 ECs (including 117 endometrioid G3), 31 SCs, and 38 CCs. The prognostic implication of the percentage of each component was analyzed. Among the 69 MECs, those patients older than 45 years represent the significant population, with 52.2% of them with stage III-IV disease. A similar result was found among pure SC. The comparative analysis of some prognostic parameters (multifocality, vascular invasion, and lymph node metastasis) underlined that MECs with a type II component larger than 5% represent a more aggressive entity. However, relapse, disease-free survival, mortality, and overall survival are statistically significant (PÂ <Â .05) in EC-SC (SCÂ <5%Â or >5%) and in EC-CC (CCÂ <5%Â or >5%), whereas they are not significant (PÂ >Â .05) in SC-CC (SC/CCÂ <%Â or >5%). MECs, including also cases with less than 5% of SC/CC, show features as aggressive as those of pure SC/CC. In this perspective, MEC should be followed by personalized and tailored managements. The presence of different components suggests different pathogenic and metastatic processes when compared with pure carcinomas.
AB - Mixed endometrial carcinomas (MECs) refer to tumors characterized by 2 or more distinct histotypes mostly that comprised endometrioid (EC) and serous/clear cell carcinomas (SC/CC). The specific quantification of these distinct components represents a challenging and critical point for both prognosis and management. Herein, we analyze a large series of MEC and compare them with EC and SC/CC. We evaluated a series of 69 MECs between January 2002 and December 2015. We compared the MEC series with 186 ECs (including 117 endometrioid G3), 31 SCs, and 38 CCs. The prognostic implication of the percentage of each component was analyzed. Among the 69 MECs, those patients older than 45 years represent the significant population, with 52.2% of them with stage III-IV disease. A similar result was found among pure SC. The comparative analysis of some prognostic parameters (multifocality, vascular invasion, and lymph node metastasis) underlined that MECs with a type II component larger than 5% represent a more aggressive entity. However, relapse, disease-free survival, mortality, and overall survival are statistically significant (PÂ <Â .05) in EC-SC (SCÂ <5%Â or >5%) and in EC-CC (CCÂ <5%Â or >5%), whereas they are not significant (PÂ >Â .05) in SC-CC (SC/CCÂ <%Â or >5%). MECs, including also cases with less than 5% of SC/CC, show features as aggressive as those of pure SC/CC. In this perspective, MEC should be followed by personalized and tailored managements. The presence of different components suggests different pathogenic and metastatic processes when compared with pure carcinomas.
KW - 2734
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Biopsy
KW - Carcinoma, Endometrioid
KW - Clear cell carcinomas
KW - Disease-Free Survival
KW - Endometrial Neoplasms
KW - Endometrial tumor
KW - Female
KW - Humans
KW - Immunohistochemistry
KW - Kaplan-Meier Estimate
KW - Middle Aged
KW - Mixed endometrial carcinomas
KW - Molecular testing
KW - Neoplasm Recurrence, Local
KW - Neoplasm Staging
KW - Neoplasms, Complex and Mixed
KW - Neoplasms, Cystic, Mucinous, and Serous
KW - Predictive Value of Tests
KW - Serous carcinomas
KW - Time Factors
KW - Treatment Outcome
KW - Type I carcinomas
KW - Type II carcinomas
KW - 2734
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Biopsy
KW - Carcinoma, Endometrioid
KW - Clear cell carcinomas
KW - Disease-Free Survival
KW - Endometrial Neoplasms
KW - Endometrial tumor
KW - Female
KW - Humans
KW - Immunohistochemistry
KW - Kaplan-Meier Estimate
KW - Middle Aged
KW - Mixed endometrial carcinomas
KW - Molecular testing
KW - Neoplasm Recurrence, Local
KW - Neoplasm Staging
KW - Neoplasms, Complex and Mixed
KW - Neoplasms, Cystic, Mucinous, and Serous
KW - Predictive Value of Tests
KW - Serous carcinomas
KW - Time Factors
KW - Treatment Outcome
KW - Type I carcinomas
KW - Type II carcinomas
UR - http://hdl.handle.net/10807/111160
UR - http://www.elsevier.com/inca/publications/store/6/2/3/1/3/9/index.htt
U2 - 10.1016/j.humpath.2016.12.015
DO - 10.1016/j.humpath.2016.12.015
M3 - Article
SN - 0046-8177
VL - 62
SP - 99
EP - 107
JO - Human Pathology
JF - Human Pathology
ER -