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Preoperative and pre-chemotherapy CA-125 levels in high-risk early-stage ovarian cancer - An NRG/GOG study.
Chan, John K; Tian, Chunqiao; Kesterson, Joshua P; Lin, Ken Y; Darcy, Kathleen; Richardson, Michael T; Kapp, Daniel S; Monk, Bradley J; McNally, Leah; Landrum, Lisa; Copeland, Larry; Walker, Joan L; Wenham, Robert M; Phippen, Neil; Spirtos, Nick M; Tewari, Krishnansu; Shahin, Mark; Berry, Laurel; Bell, Jeffery G.
Affiliation
  • Chan JK; California Pacific/Palo Alto Medical Foundation/Sutter Research Institute, San Francisco, CA, USA. Electronic address: chanjohn@sutterhealth.org.
  • Tian C; NRG Statistical Center, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
  • Kesterson JP; Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA. Electronic address: kestersonjp@upmc.edu.
  • Lin KY; Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Darcy K; NRG Statistical Center, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA. Electronic address: darcyk@whirc.org.
  • Richardson MT; University of California, Los Angeles School of Medicine, Los Angeles, CA, USA. Electronic address: mtrichardson@mednet.ucla.edu.
  • Kapp DS; Stanford University School of Medicine, Stanford, CA, USA. Electronic address: dskapp@stanford.edu.
  • Monk BJ; HonorHealth Research Institute, University of Arizona, Creighton University, Phoenix, AZ, USA. Electronic address: bmonk@gog.org.
  • McNally L; Duke University, Durham, NC, USA. Electronic address: leah.mcnally018@duke.edu.
  • Landrum L; Indiana University, Indianapolis, IN, USA. Electronic address: llandru@iu.edu.
  • Copeland L; Ohio State University Comprehensive Cancer Center, Columbus, OH, USA. Electronic address: Larry.Copeland@osumc.edu.
  • Walker JL; University of Oklahoma, Oklahoma City, OH, USA. Electronic address: joan-walker@ouhsc.edu.
  • Wenham RM; Moffitt Cancer Center and Research Institute, Tampa, FL, USA. Electronic address: Robert.wenham@moffitt.org.
  • Phippen N; Walter Reed National Military Medical Center, Bethesda, MD, USA. Electronic address: neil.phippen@usuhs.edu.
  • Spirtos NM; Womens Cancer Center of Nevada, Las Vegas, NV, USA. Electronic address: nmspirtos@wccenter.com.
  • Tewari K; University of California Medical Center at Irvine, Irvine, CA, USA. Electronic address: ktewari@hs.uc.edu.
  • Shahin M; Abington Memorial Hospital, Abington, PA, USA. Electronic address: Mark.Shahin@jefferson.edu.
  • Berry L; Wake Forest University Health Sciences, Winston-Salem, NC, USA. Electronic address: lkberry@wakehealth.edu.
  • Bell JG; Ohio Riverside Methodist Hospital, Columbus, OH, USA.
Gynecol Oncol ; 181: 54-59, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38134754
ABSTRACT

OBJECTIVES:

To determine clinical significance of preoperative and pre-chemotherapy CA-125 in high-risk early-stage epithelial ovarian cancer patients.

METHODS:

All patients with stage IA/IB and grade 3, stage IC, clear cell, or completed resected stage II cancer were enrolled in a phase III trial and treated with chemotherapy. Kaplan-Meier method and Cox proportional hazards model were used for statistical analyses.

RESULTS:

427 patients with high-risk early-stage ovarian cancer were enrolled. Of 213 patients with preoperative CA-125 data, 79% had elevated CA-125. Median preoperative CA-125 level was 103 U/mL. Patients with ≤10, 11-15, and > 15 cm tumors had median preoperative CA-125 levels of 62, 131 and 158 U/mL, respectively (p = 0.002). For the 350 patients with data for pre-chemotherapy CA-125 level, 69% had elevated pre-chemotherapy CA-125 above 35 U/mL with median value of 65 U/mL. However, age, race, stage, cell type and grade of disease were not correlated with CA-125 levels before and after surgery. On multivariate analysis, elevated pre-chemotherapy CA-125 independently predicted worse recurrence-free survival (HR = 2.13, 95% CI 1.23-3.69; p = 0.007) and overall survival (HR = 1.99, 95% CI 1.10-3.59; p = 0.022) after adjusting for age, stage, cell type and grade of disease. Compared to those with normal CA-125, patients with elevated pre-chemotherapy CA-125 had lower recurrence-free survival (RFS, 87% vs. 75%; p = 0.007) and overall survival (OS, 88% vs. 82%; p = 0.02). However, preoperative CA-125 was not prognostic of RFS (p = 0.699) or OS (p = 0.701).

CONCLUSIONS:

Preoperative CA-125 was elevated in nearly 80% of high-risk early-stage ovarian cancer patients. Pre-chemotherapy CA-125 was associated with recurrence-free and overall survival; however, preoperative CA-125 was not prognostic.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms Limits: Female / Humans Language: En Journal: Gynecol Oncol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms Limits: Female / Humans Language: En Journal: Gynecol Oncol Year: 2024 Document type: Article