Published January 1, 2008 | Version v1
Journal article

Are Increased Tumor Aneuploidy and Heightened Cell Proliferation Along With Heterogeneity Associated With Patient Outcome for Carcinomas of the Uterine Cervix? A Combined Analysis of Subjects Treated in RTOG 9001 and a Single-Institution Trial

  • 1. Department of Radiation Oncology, University of Miami Miller School of Medicine, Miami, FL (United States)
  • 2. Statistical Office, Radiation Therapy Oncology Group, Philadelphia, PA (United States)

Description

Purpose: To look for possible associations between measurements of DNA index (DI), S-phase fraction (SPF), and tumor heterogeneity (TH) using flow cytometry and overall survival for patients with invasive cervical carcinoma treated with definitive irradiation. Methods and Materials: A total of 57 patients with International Federation of Obstetrics and Gynecology Stages IB2 through IVB cervical carcinomas treated with definitive radiotherapy with or without concurrent chemotherapy were enrolled into this registry study that involved flow cytometric analysis of fresh tissue from each cervical cancer obtained by pretreatment biopsy. These specimens were evaluated for DNA aneuploidy (DI ≤1.5 vs. >1.5), SPF (≤15% vs. >15%), and TH (uniploid vs. multiploid). Results: In these analyses 27 of the patients were treated in Radiation Therapy Oncology Group protocol 9001, and an additional 30 were offered chemoradiation at a single institution. Forty-one patients had DI ≤1.5 and 16 DI >1.5. Twenty-nine patients had SPF ≤15%, 26 >15%, and 2 had no determinable SPF. Forty-three patients had uniploid and 14 multiploid tumors. The 4-year estimated overall survival rate for the entire study cohort was 62% (95% confidence interval 48%-74%). With a median follow-up of 3.7 years, there were no observable associations by univariate analysis for DI, SPF, or TH concerning patient survival. Conclusions: There were no statistically significant associations among DI, SPF, or TH and patient outcome. Additional studies are indicated to identify tumor biomarkers that could predict patients at risk for disseminated disease

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2007.05.069

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2007.05.069;
PII
S0360-3016(07)01027-9;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
70
Journal Issue
1
Journal Page Range
p. 111-117
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
39059707
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANEUPLOIDY; BIOLOGICAL MARKERS; BIOPSY; CARCINOMAS; CELL PROLIFERATION; CHEMOTHERAPY; DNA; FIRE HAZARDS; GYNECOLOGY; IRRADIATION; PATIENTS; RADIOTHERAPY
Descriptors DEC
DIAGNOSTIC TECHNIQUES; DISEASES; HAZARDS; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; NUCLEIC ACIDS; ORGANIC COMPOUNDS; PLOIDY; RADIOLOGY; THERAPY

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, Netherlands, All rights reserved.