Ki67 does not predict recurrence for low-grade appendiceal mucinous neoplasms with peritoneal dissemination after cytoreductive surgery and HIPEC.
Adenocarcinoma, Mucinous
/ chemistry
Adult
Aged
Aged, 80 and over
Appendiceal Neoplasms
/ chemistry
Chemotherapy, Adjuvant
Cytoreduction Surgical Procedures
/ adverse effects
Databases, Factual
Female
Humans
Hyperthermic Intraperitoneal Chemotherapy
/ adverse effects
Ki-67 Antigen
/ analysis
Male
Middle Aged
Neoplasm Grading
Neoplasm Recurrence, Local
Peritoneal Neoplasms
/ chemistry
Progression-Free Survival
Retrospective Studies
Risk Assessment
Risk Factors
Time Factors
Cytoreductive surgery
Hyperthermic intraperitoneal chemotherapy
Ki67
Low-grade mucinous carcinoma peritonei
Journal
Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
received:
04
02
2021
revised:
16
04
2021
accepted:
19
04
2021
pubmed:
28
4
2021
medline:
29
12
2021
entrez:
27
4
2021
Statut:
ppublish
Résumé
Low-grade appendiceal mucinous neoplasms (LAMN) can disseminate to become low-grade mucinous carcinoma peritonei (LGMCP), which is optimally treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC). Approximately half of the patients with LGMCP recur despite complete cytoreduction, and risk factors for recurrence are poorly understood. We sought to evaluate if Ki67 predicts progression of LGMCP after CRS/HIPEC. A retrospective review of a prospectively maintained database was performed to identify patients treated with complete CRS/HIPEC for LGMCP from 2008 to 2019 with Ki67 assessed. Patient characteristics, histologic data, average and focally high "hotspot") Ki67 index, progression-free survival (PFS), and overall survival (OS) were analyzed. Ki-67 immunostain was performed on the histologic section with the highest cellularity and architectural complexity. Forty-four patients with LGMCP (55% male, median age 61) were identified. The median Ki67 score and hotspot Ki67 score was 15% (1-70) and 50% (1-90), respectively. On univariate analysis, average Ki67 and hotspot Ki67 were not predictive of PFS when analyzed as continuous normalized values (HR 1.0, p = 0.79 and HR 1.1, p = 0.38, respectively) or as categorical values when stratified by the median (HR 0.9, p = 0.67 and HR 1.0, p = 0.93). This remained true on multivariate analysis when stratified for peritoneal cancer index, CEA, and completeness of cytoreduction score for both normalized Ki67 and hotspot Ki67 (HR 0.9 [95% CI 0.8-1.3], p = 0.94 and HR 1.04 [95% CI 0.8-1.3], p = 0.73, respectively). Ki67 failed to predict disease recurrence for patients with LGMCP in this cohort.
Identifiants
pubmed: 33905776
pii: S0046-8177(21)00064-2
doi: 10.1016/j.humpath.2021.04.007
pii:
doi:
Substances chimiques
Ki-67 Antigen
0
MKI67 protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
104-110Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.