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An evaluation of progression free survival and overall survival of ovarian cancer patients with clear cell carcinoma versus serous carcinoma treated with platinum therapy: An NRG Oncology/Gynecologic Oncology Group experience.
Oliver, Kate E; Brady, William E; Birrer, Michael; Gershenson, David M; Fleming, Gini; Copeland, Larry J; Tewari, Krishnansu; Argenta, Peter A; Mannel, Robert S; Secord, Angeles Alvarez; Stephan, Jean-Marie; Mutch, David G; Stehman, Frederick B; Muggia, Franco M; Rose, Peter G; Armstrong, Deborah K; Bookman, Michael A; Burger, Robert A; Farley, John H.
Afiliação
  • Oliver KE; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Naval Medical Center Portsmouth, 620 John Paul Jones Cir, Portsmouth, VA 23708, United States. Electronic address: kate.e.oliver.mil@mail.mil.
  • Brady WE; NRG Oncology Statistics and Data Management Center, Roswell Park Cancer Institute, Buffalo, NY 14263, United States. Electronic address: bbrady@gogstats.org.
  • Birrer M; Massachusetts General Hospital, Boston, MA 02114, United States. Electronic address: MBIRRER@mgh.harvard.edu.
  • Gershenson DM; Department of Gynecologic Oncology, University of Texas, MD Anderson Cancer Center, Houston, TX, United States. Electronic address: dgershen@mdanderson.org.
  • Fleming G; University of Chicago, 5841 S. Maryland Avenue, Chicago, IL, United States. Electronic address: gfleming@medicine.bsd.uchicago.edu.
  • Copeland LJ; The Ohio State University, Columbus, OH, United States. Electronic address: larry.copeland@osumc.edu.
  • Tewari K; Obstetrics-Gynecology, University of California, Irvine, Orange, CA, United States. Electronic address: ktewari@uci.edu.
  • Argenta PA; University of Minnesota Medical Center, Minneapolis, MN, United States. Electronic address: argenta@umn.edu.
  • Mannel RS; University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States. Electronic address: robert-mannel@ouhsc.edu.
  • Secord AA; Gynecologic Oncology, Duke Medical Center, Durham, NC, United States. Electronic address: angeles.secord@duke.edu.
  • Stephan JM; University of Iowa Hospitals and Clinics, Iowa City, IA, United States. Electronic address: jean-marie-stephan@uiowa.edu.
  • Mutch DG; Washington University, United States. Electronic address: mutchd@wudosis.wustl.edu.
  • Stehman FB; Indiana University Hospital, Indianapolis, IN, United States. Electronic address: fstehman@iupui.edu.
  • Muggia FM; NYU Clinical Cancer Center, New York, NY, United States. Electronic address: franco.muggia@nyumc.org.
  • Rose PG; Cleveland Clinic, Cleveland, OH, United States. Electronic address: rosep@ccf.org.
  • Armstrong DK; Medical Oncology and Gynecology and Obstetrics, Johns Hopkins Kimmel Cancer Center, Baltimore, MD, United States. Electronic address: ARMSTDE@jhmi.edu.
  • Bookman MA; US Oncology Research and Arizona Oncology, Tucson, AZ, United States. Electronic address: Michael.bookman@usoncology.com.
  • Burger RA; University of Pennsylvania, Abramson Cancer Center, Philadelphia, PA, United States. Electronic address: Robert.burger@uphs.upenn.edu.
  • Farley JH; Department of Obstetrics and Gynecology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, United States. Electronic address: John.farley@chw.edu.
Gynecol Oncol ; 147(2): 243-249, 2017 11.
Article em En | MEDLINE | ID: mdl-28807367
ABSTRACT

PURPOSE:

We examined disparities in prognosis between patients with ovarian clear cell carcinoma (OCCC) and serous epithelial ovarian cancer (SOC).

METHODS:

We reviewed data from FIGO stage I-IV epithelial ovarian cancer patients who participated in 12 prospective randomized GOG protocols. Proportional hazards models were used to compare progression-free survival (PFS) and overall survival (OS) by cell type (clear cell versus serous).

RESULTS:

There were 10,803 patients enrolled, 9531 were eligible, evaluable and treated with platinum, of whom 544 (6%) had OCCC, 7054 (74%) had SOC, and 1933 (20%) had other histologies and are not included further. In early stage (I-II) patients, PFS was significantly better in OCCC than in SOC patients. For late stage (III, IV) patients, OCCC had worse PFS and OS compared to SOC, OS HR=1.66 (1.43, 1.91; p<0.001). After adjusting for age and stratifying by protocol and treatment arm, stage, performance status, and race, OCCC had a significantly decreased OS, HR=1.53 (1.33, 1.76; p<0.001). In early stage cases, there was a significantly decreased treatment effect on PFS for consolidative therapy with weekly Paclitaxel versus observation in OCCC compared to SOC (p=0.048).

CONCLUSIONS:

This is one of the largest analyses to date of OCCC treated on multiple cooperative group trials. OCCC histology is more common than SOC in early stage disease. When adjusted for prognostic factors, in early stage patients, PFS was better for OCCC than for SOC; however, in late-stage patients, OCCC was significantly associated with decreased OS. Finally, treatment effect was influenced by histology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Protocolos de Quimioterapia Combinada Antineoplásica / Cistadenocarcinoma Seroso / Adenocarcinoma de Células Claras Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Gynecol Oncol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Protocolos de Quimioterapia Combinada Antineoplásica / Cistadenocarcinoma Seroso / Adenocarcinoma de Células Claras Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Gynecol Oncol Ano de publicação: 2017 Tipo de documento: Article