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Clinical calculator redefines prognosis for high-risk early-stage ovarian cancers and potential to guide treatment in the adjuvant setting.
Bui, Anthony; Gehrig, Paola A; Ghamande, Sharad; Rungruang, Bunja J; Chan, John K; Mysona, David P.
Afiliação
  • Bui A; The University of North Carolina, Chapel Hill, NC, USA.
  • Gehrig PA; The University of North Carolina, Chapel Hill, NC, USA; University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.
  • Ghamande S; Medical College of Georgia, Augusta, GA, USA.
  • Rungruang BJ; Medical College of Georgia, Augusta, GA, USA.
  • Chan JK; California Pacific & Palo Alto Medical Foundation/Sutter Health Research Institute, San Francisco, CA, USA; Palo Alto Medical Foundation Research Institute, Palo Alto, CA, USA.
  • Mysona DP; The University of North Carolina, Chapel Hill, NC, USA; Medical College of Georgia, Augusta, GA, USA. Electronic address: David.Mysona@augusta.edu.
Gynecol Oncol ; 167(2): 205-212, 2022 11.
Article em En | MEDLINE | ID: mdl-36055814
ABSTRACT

OBJECTIVE:

To determine the utility of a clinical calculator to redefine prognosis and need for chemotherapy among patients with early-stage high-risk epithelial ovarian cancer.

METHODS:

Data were abstracted for stage I-II, high-risk ovarian cancer from the National Cancer Database from years 2005 to 2015. Based on demographic, pathologic, surgical, and laboratory characteristics, a clinical score was developed using Cox regression. Propensity score weighting was used to adjust for differences between patients who did and did not receive chemotherapy.

RESULTS:

Of 8188 patients with early-stage high-risk ovarian cancer, 6915 (84%) did and 1273 (16%) did not receive chemotherapy. A clinical calculator was created utilizing age, stage, histology, grade, tumor size, number of pelvic and paraaortic lymph nodes examined, the presence of malignant ascites, and CA125. The calculator divided patients into low, moderate, and high-risk groups with 5-year OS (overall survival) of 92%, 82%, and 66%, and 10-year OS of 85%, 67%, and 44%, respectively. Chemotherapy improved 5-year OS and 10-year OS in the high-risk group (56% to 73%; p < 0.001, 34% to 48%; p < 0.001). The moderate risk group had improved 5-year OS (80% to 85%; p = 0.01) but not 10-year OS (66% to 66%; p = 0.13). Chemotherapy did not improve 5-year or 10-year OS in low-risk patients (93% to 92%, p = 1.0, 86% to 84%, p = 0.99).

CONCLUSIONS:

The prognosis among high-risk early-stage ovarian cancer patients is heterogeneous. This calculator may aid in patient-centered counseling regarding potential treatment benefits.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos