Ki67 does not predict recurrence for low-grade appendiceal mucinous neoplasms with peritoneal dissemination after cytoreductive surgery and HIPEC.


Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
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

104-110

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Erin P Ward (EP)

Medical College of Wisconsin, 53226, USA. Electronic address: eward@mcw.edu.

Luke Okamuro (L)

University of California San Diego, 92037, USA.

Sohini Khan (S)

University of California San Diego, 92037, USA.

Morgan Hosseini (M)

University of California San Diego, 92037, USA.

Mark A Valasek (MA)

University of California San Diego, 92037, USA.

Nemencio Ronquillo (N)

University of Louisville, 40292, USA.

Kaitlyn J Kelly (KJ)

University of California San Diego, 92037, USA.

Jula Veerapong (J)

University of California San Diego, 92037, USA.

Andrew M Lowy (AM)

University of California San Diego, 92037, USA.

Joel Baumgartner (J)

University of California San Diego, 92037, USA.

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Classifications MeSH