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. 2024 Sep 27;16(19):3295.
doi: 10.3390/cancers16193295.

The Predictive Value of the Fibrinogen-Albumin-Ratio Index on Surgical Outcomes in Patients with Advanced High-Grade Serous Ovarian Cancer

Affiliations

The Predictive Value of the Fibrinogen-Albumin-Ratio Index on Surgical Outcomes in Patients with Advanced High-Grade Serous Ovarian Cancer

Magdalena Postl et al. Cancers (Basel). .

Abstract

Background/objectives: The present study evaluates predictive implications of the pretherapeutic Fibrinogen-Albumin-Ratio Index (FARI) in high-grade serous ovarian cancer (HGSOC) patients undergoing primary cytoreductive surgery.

Methods: This retrospective study included 161 patients with HGSOC International Federation of Gynecology and Obstetrics (FIGO) stage ≥ IIb, who underwent primary cytoreductive surgery followed by platinum-based chemotherapy. Associations between the FARI and complete tumor resection status were described by receiver operating characteristics, and binary logistic regression models were fitted.

Results: Higher preoperative FARI values correlated with higher ascites volumes (r = 0.371, p < 0.001), and higher CA125 levels (r = 0.271, p = 0.001). A high FARI cut at its median (≥11.06) was associated with lower rates of complete tumor resection (OR 3.13, 95% CI [1.63-6.05], p = 0.001), and retrained its predictive value in a multivariable model independent of ascites volumes, CA125 levels, FIGO stage, and Charlson Comorbidity Index (CCI).

Conclusions: The FARI appears to act as a surrogate for higher intra-abdominal tumor load. After clinical validation, FARI could serve as a readily available serologic biomarker to complement preoperative patient assessment, helping to identify patients who are likely to achieve complete tumor resection during primary cytoreductive surgery.

Keywords: FARI; HGSOC; albumin; cytoreductive surgery; fibrinogen; neoadjuvant chemotherapy; ovarian cancer; tumor load.

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Conflict of interest statement

Nicole Concin: Payment or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing, or educational events: GSK, SEAGEN, Akesobio, AstraZeneca, eTheRNA, immunotherapies NV, Kartos, MSD, Mersana, ImmunoGen, EISAI, Seattle Genetics, TouchIME, Medscape Oncology; Support for attending meetings and/or travel: Roche, Genmab, Amgen; Participation on a data safety monitoring board or advisory board: GSK, Mersana, SEAGEN, ImmunoGen, Akesobio, EISAI, AstraZeneca, Mersana, Seattle Genetics, eTheRNA immunotherapies NV, Kartos; Leadership or fiduciary role in other board, society, committee, or advocacy groups, paid or unpaid: President—ESGO, Chair—ENGOT Early Drug Development Network, FIGO board member for women’s cancer. Stephan Polterauer: Payment or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing, or educational events: Astra Zeneca, GSK, MSD; Support for attending meetings and/or travel: Astra Zeneca; Leadership or fiduciary role in other board, society, committee, or advocacy groups, paid or unpaid: AGO Austria secretary. All other authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Consort diagram depicting all patients with ovarian cancer undergoing primary treatment who were not included into final analysis (n = 1013/1174, 86.3%). HGSOC, high-grade serous ovarian cancer; FIGO, International Federation of Gynaecology and Obstetrics.
Figure 2
Figure 2
(a) A high FARI ≥ 11.06 is associated with impaired progression-free survival in patients with advanced high-grade serous ovarian cancer. The yellow line depicts patients with a FARI < 11.06 and the blue line depicts patients with a FARI ≥ 11.06, with 95% confidence intervals, respectively. (b) A high FARI ≥ 11.06 is associated with impaired disease-specific survival in patients with advanced high-grade serous ovarian cancer. The yellow line depicts patients with a FARI < 11.06 and the blue line depicts patients with a FARI ≥ 11.06, with 95% confidence intervals, respectively.

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