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Correlation of imaging and plasma based biomarkers to predict response to bevacizumab in epithelial ovarian cancer (EOC).
Buechel, Megan E; Enserro, Danielle; Burger, Robert A; Brady, Mark F; Wade, Katrina; Secord, Angeles Alvarez; Nixon, Andrew B; Mirniaharikandehei, Seyedehnafiseh; Liu, Hong; Zheng, Bin; O'Malley, David M; Gray, Heidi; Tewari, Krishnansu S; Mannel, Robert S; Birrer, Michael J; Moore, Kathleen N.
Affiliation
  • Buechel ME; Stephenson Cancer Center, The University of Oklahoma Health Sciences Center, Section of Gynecologic Oncology, Oklahoma City, OK, United States of America. Electronic address: MEBuechel@gmail.com.
  • Enserro D; NRG Oncology SDMC, CTD Division, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: enserrod@nrgoncology.org.
  • Burger RA; University of Pennsylvania, Philadelphia, PA, United States of America. Electronic address: Robert.Burger@uphs.upenn.edu.
  • Brady MF; NRG Oncology SDMC, CTD Division, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: bradym@nrgoncology.org.
  • Wade K; Oschner Medical Center, New Orleans, LA, United States of America. Electronic address: katrina.wade@ochsner.org.
  • Secord AA; Duke University, Division of Gynecologic Oncology, Durham, NC, United States of America. Electronic address: angeles.secord@duke.edu.
  • Nixon AB; Duke University, Division of Medical Oncology, Durham, NC, United States of America. Electronic address: anixon@duke.edu.
  • Mirniaharikandehei S; University of Oklahoma, Department of Electrical and Computer Engineering, Norman, OK, United States of America. Electronic address: snmirna@ou.edu.
  • Liu H; University of Oklahoma, Department of Electrical and Computer Engineering, Norman, OK, United States of America. Electronic address: liu@ou.edu.
  • Zheng B; University of Oklahoma, Department of Electrical and Computer Engineering, Norman, OK, United States of America. Electronic address: bin.zheng-1@ou.edu.
  • O'Malley DM; James Cancer Center at the Ohio State University, Columbus, OH, United States of America. Electronic address: omalley.46@osu.edu.
  • Gray H; University of Washington, Seattle, WA, United States of America. Electronic address: hgray@uw.edu.
  • Tewari KS; University of California, Irvine, CA, , United States of America. Electronic address: ktewari@uci.edu.
  • Mannel RS; Stephenson Cancer Center, The University of Oklahoma Health Sciences Center, Section of Gynecologic Oncology, Oklahoma City, OK, United States of America. Electronic address: Robert-Mannel@ouhsc.edu.
  • Birrer MJ; University of Alabama, Birmingham, AL, United States of America. Electronic address: mbirrer@uabmc.edu.
  • Moore KN; Stephenson Cancer Center, The University of Oklahoma Health Sciences Center, Section of Gynecologic Oncology, Oklahoma City, OK, United States of America. Electronic address: Kathleen-Moore@ouhsc.edu.
Gynecol Oncol ; 161(2): 382-388, 2021 05.
Article in En | MEDLINE | ID: mdl-33712274
PURPOSE: Increasing measures of adiposity have been correlated with poor oncologic outcomes and a lack of response to anti-angiogenic therapies. Limited data exists on the impact of subcutaneous fat density (SFD) and visceral fat density (VFD) on oncologic outcomes. This ancillary analysis of GOG-218, evaluates whether imaging markers of adiposity were predictive biomarkers for bevacizumab (bev) use in epithelial ovarian cancer (EOC). PATIENTS AND METHODS: There were 1249 patients (67%) from GOG-218 with imaging measurements. SFD and VFD were calculated utilizing Hounsfield units (HU). Proportional hazards models were used to assess the association between SFD and VFD with overall survival (OS). RESULTS: Increased SFD and VFD showed an increased HR for death (HR per 1-SD increase 1.12, 95% CI:1.05-1.19 p = 0.0009 and 1.13, 95% CI: 1.05-1.20 p = 0.0006 respectively). In the predictive analysis for response to bev, high VFD showed an increased hazard for death in the placebo group (HR per 1-SD increase 1.22, 95% CI: 1.09-1.37; p = 0.025). However, in the bev group there was no effect seen (HR per 1-SD increase: 1.01, 95% CI: 0.90-1.14) Median OS was 45 vs 47 months in the VFD low groups and 36 vs 42 months in the VFD high groups on placebo versus bev, respectively. CONCLUSION: High VFD and SFD have a negative prognostic impact on patients with EOC. High VFD appears to be a predictive marker of bev response and patients with high VFD may be more likely to benefit from initial treatment with bev.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Biomarkers, Tumor / Intra-Abdominal Fat / Subcutaneous Fat / Bevacizumab / Antineoplastic Agents, Immunological / Carcinoma, Ovarian Epithelial Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Gynecol Oncol Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Biomarkers, Tumor / Intra-Abdominal Fat / Subcutaneous Fat / Bevacizumab / Antineoplastic Agents, Immunological / Carcinoma, Ovarian Epithelial Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Gynecol Oncol Year: 2021 Type: Article