Jenary Immanuel Surbakti
Obstetric and Gynaecology Specialist, Bagan Batu, Rokan Hilir Riau, Indonesia / Graduate of Faculty of Medicine, University of North Sumatera, Indonesia

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Is there an association between ultra-processed food consumption and ovarian cancer risk in women? : A Systematic Review Amanda Ezra Natasya Napitupulu; Jenary Immanuel Surbakti
The International Journal of Medical Science and Health Research Vol. 41 No. 2 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/p2g9ps32

Abstract

Introduction: Ultra-processed foods (UPF) have been implicated in chronic disease development, but their association with ovarian cancer—a leading cause of gynecologic cancer mortality—requires systematic evaluation. This review examines evidence linking UPF consumption to ovarian cancer risk. Methods: We systematically reviewed observational studies assessing UPF consumption (using NOVA classification or quantitative methods) and ovarian cancer incidence or mortality in adult women. Nine studies met inclusion criteria. Results: The UK Biobank prospective cohort (197,426 participants; 143 ovarian cancer cases; 9.8 years follow-up) demonstrated significant positive associations between UPF consumption and ovarian cancer incidence (HR 1.19 per 10% increment; 95% CI: 1.08–1.30; p<0.001) and mortality (HR 1.30; 95% CI: 1.13–1.50). Supporting evidence from case-control studies showed preserved foods consumption (>13.5 g/day) was associated with 78% increased odds of epithelial ovarian cancer (OR 1.78; 95% CI: 1.35–2.34), while a "meat and fat" dietary pattern was associated with 2.5-fold increased risk (OR 2.49; 95% CI: 1.75–3.55). Brazilian cross-sectional studies identified UPF consumption among ovarian cancer survivors, particularly those under 40 years. Discussion: The positive association observed in the UK Biobank persisted after adjustment for multiple confounders including age, BMI, reproductive factors, and socioeconomic status. The consistency across different dietary exposures—UPF, preserved foods, and high-fat dietary patterns—suggests that processed and energy-dense foods may contribute to ovarian carcinogenesis through multiple pathways, potentially including inflammation, insulin resistance, and endocrine disruption. BMI adjustment in the Kolahdooz study strengthened the observed association, indicating mechanisms independent of adiposity. Conclusion: Evidence supports a positive association between consumption of ultra-processed and processed foods and increased ovarian cancer risk. Further research should identify specific UPF subgroups and vulnerable populations.
How does primary debulking surgery compared to neoadjuvant chemotherapy followed by interval debulking surgery affect overall survival in women with advanced ovarian cancer? : A Systematic Review Amanda Ezra Natasya Napitupulu; Jenary Immanuel Surbakti
The International Journal of Medical Science and Health Research Vol. 42 No. 1 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/zrxd4092

Abstract

Introduction: Advanced epithelial ovarian cancer (stage III-IV) remains a leading cause of gynecologic cancer mortality worldwide. The optimal initial treatment approach—primary debulking surgery (PDS) versus neoadjuvant chemotherapy followed by interval debulking surgery (NACT-IDS)—continues to generate substantial clinical debate despite multiple randomized trials. This systematic review aims to compare overall survival outcomes between PDS and NACT-IDS in women with advanced ovarian cancer. Methods: A systematic review was conducted following PRISMA guidelines. We screened studies based on predefined criteria: inclusion of women ≥18 years with FIGO stage III-IV epithelial ovarian cancer, direct comparison of PDS versus NACT-IDS, reporting of overall survival outcomes, and study designs including randomized controlled trials, cohort studies, systematic reviews, and meta-analyses. Data extraction encompassed study characteristics, patient selection criteria, treatment details, survival outcomes, surgical outcomes, and subgroup analyses. Results: Eighty studies were included, comprising five major RCTs (EORTC 55971, CHORUS, SCORPION, JCOG0602, TRUST) and numerous meta-analyses and observational studies. Meta-analyses demonstrated no significant difference in overall survival between PDS and NACT-IDS (HR 0.96, 95% CI 0.86-1.08) [1-3]. Individual RCTs confirmed similar findings: EORTC 55971 (HR 0.98, 90% CI 0.84-1.13) [4], CHORUS (HR 0.87, 95% CI 0.72-1.05) [5], and TRUST (HR 0.89, 95% CI 0.74-1.08) [6]. However, NACT-IDS achieved superior complete cytoreduction rates (RR 2.34, 95% CI 1.48-3.71) [2] with significantly lower perioperative mortality (RR 0.16, 95% CI 0.06-0.46) and major complications (RR 0.22, 95% CI 0.13-0.38) [1]. Observational studies consistently favored PDS, reflecting selection bias [7,8]. Stage-specific analysis revealed NACT-IDS benefited stage IV disease (HR 0.76, 95% CI 0.58-1.00) [9], while PDS showed advantage in stage III with limited metastatic burden [6,8]. Discussion: The apparent contradiction between RCT and observational evidence reflects fundamental differences in patient selection, surgical quality, and study design. Complete cytoreduction at PDS identifies a biologically favorable subset with superior outcomes, whereas achieving complete resection after NACT may indicate chemotherapy responsiveness without equivalent survival benefit. NACT-IDS offers clear perioperative safety advantages, making it preferable for unresectable disease, poor performance status, and extensive stage IV disease. Optimal treatment selection requires accurate preoperative assessment of resectability, patient fitness, and surgical expertise. Conclusion: PDS and NACT-IDS provide comparable overall survival in advanced ovarian cancer when patients are appropriately selected. PDS remains preferred when complete cytoreduction is achievable by experienced surgeons in fit patients with stage IIIC disease. NACT-IDS is a safe, effective alternative for patients with unresectable disease, poor fitness, or extensive stage IV disease. Future research should focus on validated prediction models incorporating clinical, imaging, and molecular markers to optimize individualized treatment selection.
What is the diagnostic accuracy of different clinical diagnostic criteria (Rotterdam, NIH, and Androgen Excess Society) for identifying polycystic ovary syndrome in women of reproductive age? : A Systematic Review Amanda Ezra Natasya Napitupulu; Jenary Immanuel Surbakti
The International Journal of Medical Science and Health Research Vol. 42 No. 1 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/ehpn3k33

Abstract

Introduction: Polycystic ovary syndrome (PCOS) is a complex endocrine disorder affecting women of reproductive age, with multiple diagnostic criteria currently in use including Rotterdam, NIH, and AES criteria. However, the diagnostic accuracy of these criteria remains variable across populations. This systematic review aimed to evaluate and compare the diagnostic accuracy of different clinical diagnostic criteria for identifying PCOS in reproductive-age women. Methods: A systematic review of diagnostic accuracy studies was conducted. Studies were included if they evaluated at least one of the three specified diagnostic criteria (Rotterdam, NIH, or AES) against a reference standard in women of reproductive age (15-45 years). Diagnostic accuracy measures including sensitivity, specificity, and area under the ROC curve (AUC) were extracted. The quality of included studies was assessed using appropriate diagnostic accuracy assessment tools. Results: Eighty studies encompassing diverse populations across North America, Europe, Asia, Africa, and the Middle East were included. The Rotterdam criteria demonstrated strong diagnostic utility with follicle number per ovary showing the highest accuracy (sensitivity 84%, specificity 91%, AUC 0.905). NIH criteria identified fewer women (27.1% prevalence) compared to Rotterdam (40%) and showed an AUC of 0.80 for AMH as a diagnostic marker. AES criteria yielded intermediate prevalence (29.3%) with AMH sensitivity of 84.4% and specificity of 72% (AUC 0.857). Anti-Müllerian hormone emerged as a promising biomarker with age-specific thresholds ranging from 5.7 ng/mL (20-27 years) to 3.72 ng/mL (35-40 years). Replacing PCOM with AMH in Rotterdam criteria improved diagnostic accuracy (AUC 0.934-0.97). Significant geographic and ethnic variations in optimal thresholds were observed. Discussion: The Rotterdam criteria demonstrate superior sensitivity but may overdiagnose milder phenotypes, while NIH criteria identify metabolically high-risk women with greater specificity. AES criteria provide an intermediate approach emphasizing androgen excess. Age-stratified and population-specific thresholds are essential for optimal diagnostic accuracy. AMH shows promise as an objective alternative to ultrasound assessment of PCOM. Conclusion: No single diagnostic criterion is universally optimal; the choice of criteria should be guided by clinical context, population characteristics, and available resources. Age-stratified and population-specific thresholds, particularly for AMH and ultrasound parameters, are recommended to improve diagnostic accuracy.