Pathologic stage of ypT0N+rectal cancers following neo-adjuvant treatment: clinical interpretation of an orphan status.
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Lorenzon, Laura
- De Luca, Raffaele
- Santoro, Gloria
- Parini, Dario
- Rega, Daniela
- Mellano, Alfredo
- Vigorita, Vincenzo
- Sandin, Marta
- Andriola, Valeria
- Gallo, Gaetano
- Marino, Graziella
- Turati, Luca
- Marsanic, Patrizia
- Marano, Luigi
- Lucarini, Alessio
- Aprile, Alessandra
- Sagnotta, Andrea
- Biondi, Alberto
- D'Ugo, Domenico
- Delrio, Paolo
- Balducci, Genoveffa
- Montesi, Giampaolo
- Muratore, Andrea
- Ruano Poblador, Alejandro
- Persiani, Roberto
- Roviello, Franco
- Vincenti, Leonardo
- Trompetto, Mario
- Torre, Giuseppe La
- Scala, Dario
- Sgroi, Giovanni
- Patriti, Alberto
- Simone, Michele
- Scabini, Stefano
- Mancini, Stefano
- Senior SICO Supervising Members
Grupos
Abstract
Approximately 20% of locally advanced rectal cancers treated with neoadjuvant therapy achieve a pathologic complete response, but approximately 10% of them present residual nodal metastases (ypT0N+). We aimed this research to compare the survival rates of ypT0/ypTisN+ and stage 3a rectal cancer patients. A large multicenter study recently investigated ypT0/ypTis rectal cancers treated between 2005 and 2015 in Italy and Spain. ypT0/ ypTisN+ were selected and compared with stage 3a rectal cancers treated at the same institutions with upfront surgery (ySICO group). Additionally, the SEER database was searched for patients with stage 3a rectal cancers treated with surgery in the same years. Overall survival (OS), disease-free survival (DFS), and disease-specific survival (DSS) were analyzed using Kaplan-Meier curves and random survival forest analysis (RSF). The ySICO study population consisted of 19 ypT0/2ypTisN+ (mean follow-up 41.8 months) and 72 Stage 3a patients (mean follow-up 56.9 months). These subgroups were comparable, but stage 3a patients were treated more frequently with adjuvant therapy (90.5% vs 61.9%, p 0.0001). No significant differences were reported between the ySICO subgroups for the OS, DFS, and DSS curves. When the 1213 SEER patients were added to Stage 3a, the RFS model failed to differentiate OS between groups that presented identical survival. Root analysis showed that adjuvant therapy was the only variable differentiating OS and DSS in the ySICO population. These findings suggest that ypT0/ypTisN+ and stage 3a rectal cancers could be ranked together based on their similar outcomes and pathologic assessment, and they stress the importance of adjuvant therapy in patients presenting with re-sidual nodal metastases.
Copyright © 2022 Elsevier GmbH. All rights reserved.
Datos de la publicación
- ISSN/ISSNe:
- 0344-0338, 1618-0631
- Tipo:
- Article
- Páginas:
- 154002-154002
- PubMed:
- 35849868
- Factor de Impacto:
- 0,637 SCImago ℠
- Cuartil:
- Q2 SCImago ℠
PATHOLOGY RESEARCH AND PRACTICE ELSEVIER GMBH, URBAN & FISCHER VERLAG
Documentos
- No hay documentos
Filiaciones
Keywords
- Rectal cancer; Neoadjuvant therapy; Nodal positive; Stage migration
Proyectos y Estudios Clínicos
WIBEC. WIRELESS IN-BODY ENVIRONMENT COMMUNICATIONS.
Investigador Principal: VICENTE PONS BELTRÁN
675353 . COMISION EUROPEA . 2016
MODELOS DE HÍGADO AISLADO PERFUNDIDO PARA EL RESCATE DE ÓRGANOS Y TRASLACIÓN DE LA TERAPIA GÉNICA EN EL TRASPLANTE: ESCENARIOS HUMANO "EX VIVO" Y PORCINO "IN VIVO"
Investigador Principal: RAFAEL LÓPEZ ANDÚJAR
2017_0270_CRC_LOPEZ . FUNDACION MUTUA MADRILEÑA . 2017
"TIMing Evaluation of Stoma closure” Cierre precoz vs tardío del estoma derivativo tras cirugía de cáncer de recto.
Investigador Principal: MATTEO FRASSON
2018_0078_CRC_FRASSON . ASOCIACIÓN ESPAÑOLA DE COLOPROCTOLOGÍA (AECP) . 2018
Terápia génica no-viral con 1L 10 para el tratamiento de la enfermedad inflamatoria intestinal. Estudio preliminar con piezas de cólon humano ex vivo.
Investigador Principal: MATTEO FRASSON
PI18/01658 . INSTITUTO DE SALUD CARLOS III . 2019
INDIVIDUALIZED PERIOPERATIVE HEMODYNAMIC GOAL-DIRECTED THERAPY IN MAJOR ABDOMINAL SURGERY (IPEGASUS-TRIAL).
Investigador Principal: ÓSCAR DÍAZ CAMBRONERO
IPEGASUS . 2017
MU OPIOID RECEPTOR 1 (MOR-1) EXPRESSION IN COLORECTAL CANCER AND DISEASE-FREE SURVIVAL RELATIONSHIP (MOROCCO). FIVE-YEAR FOLLOW-UP.
Investigador Principal: ÓSCAR DÍAZ CAMBRONERO
ODC-MOR-2018-01
MANAGEMENT OF ACUTE SEVERE ULCERATIVE COLITIS (MASC).
Investigador Principal: MATTEO FRASSON
MFR-CIC-2018-01 . 2019
UTILIDAD DE UNA MALLA SUPRAAPONEURÓTICA COMO PROFILAXIS DE LA EVENTRACIÓN DE LINEA MEDIA TRAS RESECCIÓN ONCOLOGICA COLORRECTAL. ESTUDIO PROSPECTIVO ALEATORIZADO MONOCÉNTRICO.
Investigador Principal: MATTEO FRASSON
PEACE . 2016
MINIMALLY INVASIVE RIGHT COLECTOMY ANASTOMOSIS STUDY (MIRCAST).
Investigador Principal: MATTEO FRASSON
MIRCAST . 2019
Cita
Lorenzon L,De Luca R,Santoro G,Parini D,Rega D,Mellano A,Vigorita V,JIMENEZ R,Sandin M,Andriola V,Gallo G,Marino G,Turati L,Marsanic P,Marano L,Lucarini A,Aprile A,Sagnotta A,Biondi A,D'Ugo D,Delrio P,Balducci G,Montesi G,Muratore A,Ruano A,Persiani R,FRASSON M,Roviello F,Vincenti L,Trompetto M,Torre GL,Scala D,Sgroi G,Patriti A,Simone M,Scabini S,Mancini S,Senior SICO Supervising M. Pathologic stage of ypT0N+rectal cancers following neo-adjuvant treatment: clinical interpretation of an orphan status. Pathol. Res. Pract. 2022. 237. p. 154002-154002. IF:2,800. (2).