The Moore Criteria: Applicability in a diverse, non-trial, recurrent cervical cancer population.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
04 2020
Historique:
received: 27 11 2019
revised: 27 12 2019
accepted: 01 01 2020
pubmed: 28 1 2020
medline: 7 10 2020
entrez: 28 1 2020
Statut: ppublish

Résumé

The Moore Criteria is a prognostic index for recurrent or metastatic cervical cancer based on five factors. The criteria were developed retrospectively and validated prospectively in clinical trial populations receiving systemic chemotherapy (C). Our objective was to evaluate the prognostic value of the Moore Criteria in a largely minority, non-trial population at first recurrence. Patients treated for recurrent cervical cancer diagnosed between 2012 and 2017 were analyzed retrospectively. Progression free survival (PFS) was defined from the date of recurrence to date of second recurrence. Overall survival (OS) was defined from the date of recurrence to date of death. Of 274 patients identified, 78 were treated in the second line. 48 (61.5%) were Hispanic, 22 (28.2%) were black, and 7 (9%) were white non-Hispanic. By Moore criteria, 9 patients (11.5%) were classified as low-risk, 48 (61.5%) as moderate risk, and 21 (26.9%) as high-risk. 53 patients (67.9%) received C, and 25 (32.1%) received other treatment modalities without C. The high-risk category carried a significantly higher hazard ratio for both PFS (5.24, p < .001) and OS (3.15, p = .002) compared with the low- and intermediate-risk combined group. The low- and intermediate-risk groups demonstrated 78.9% response rate, compared with 33.3% in the high-risk category (p = .001). Black race did not affect survival or response rate. The Moore Criteria carries prognostic value across a diverse recurrent cervical cancer population outside of the clinical trial setting. Our data suggest that in a non-trial population, black race is not predictive of worse OS or PFS.

Identifiants

pubmed: 31983517
pii: S0090-8258(20)30001-9
doi: 10.1016/j.ygyno.2020.01.001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

167-172

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors report no conflict of interest.

Auteurs

Scott E Jordan (SE)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America.

Matthew Schlumbrecht (M)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America.

Sophia George (S)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America.

J Matthew Pearson (JM)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America.

Aaron Wolfson (A)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Radiation Oncology, United States of America.

Brian Slomovitz (B)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America.

Lorraine Portelance (L)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Radiation Oncology, United States of America.

Marilyn Huang (M)

Sylvester Comprehensive Cancer Center, University of Miami, Division of Gynecologic Oncology, United States of America. Electronic address: m.huang@med.miami.edu.

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Classifications MeSH