Prognostic Value of KELIM Score and Inflammatory Markers in Ovarian Cancer
Integrative Prognostic Value of Inflammatory Markers and KELIM Score in Ovarian Cancer Patients Treated With Neoadjuvant Chemotherapy.
調査の概要
状態
研究の種類
入学 (推定)
連絡先と場所
研究場所
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Sohag、エジプト
- Sohag university hospital
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Female patients aged \ge 18 years old., Histologically confirmed advanced epithelial ovarian cancer (High-Grade Serous Ovarian Carcinoma), Stage III or IV.
Patients who received platinum-based neoadjuvant chemotherapy (NACT) followed by interval debulking surgery (IDS) at Sohag University Hospital or Sohag Cancer Center between 2022 and 2025.
Available complete medical records, including pre-treatment baseline CBC (for NLR and PLR calculation) and longitudinal CA-125 levels (for KELIM score estimation).
Exclusion Criteria:
Patients with non-epithelial ovarian tumors (e.g., germ cell tumors, sex cord-stromal tumors).
Patients who underwent primary debulking surgery (PDS) before receiving chemotherapy.
Patients with concurrent active malignancies or a history of other cancers within the past 5 years.
Patients with active systemic inflammatory diseases, hematological disorders, or severe infections at baseline that could interfere with baseline inflammatory markers (NLR/PLR).
Incomplete or missing clinical, surgical, or follow-up data.
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研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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Ovarian Cancer Cohort
Advanced serous ovarian cancer patients treated with neoadjuvant chemotherapy followed by interval debulking surgery.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Progression-Free Survival (PFS)
時間枠:From the date of diagnosis up to 4 years (assessed using retrospective medical records of patients treated between 2022 and 2025).
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Evaluation of the prognostic value of baseline neutrophil lymphocyte ratio, platelet lymphocyte ratio, and CA 125 KELIM score in predicting progression-free survival in locally advanced ovarian cancer patients receiving platinum-based neoadjuvant chemotherapy followed by interval debulking surgery.
PFS is calculated as the time from the date of diagnosis to the date of first documented clinical or radiological disease progression, or death from any cause.
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From the date of diagnosis up to 4 years (assessed using retrospective medical records of patients treated between 2022 and 2025).
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Overall Survival (OS)
時間枠:From the date of diagnosis up to 4 years (assessed using retrospective medical records of patients treated between 2022 and 2025).
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Evaluation of the prognostic value of baseline neutrophil lymphocyte ratio, platelet lymphocyte ratio, and CA 125 KELIM score in predicting overall survival in locally advanced ovarian cancer patients receiving platinum-based neoadjuvant chemotherapy followed by interval debulking surgery.
OS is calculated as the time from the date of diagnosis to the date of death from any cause.
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From the date of diagnosis up to 4 years (assessed using retrospective medical records of patients treated between 2022 and 2025).
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Completeness of Interval Cytoreductive Surgery
時間枠:At the time of interval debulking surgery (typically performed after 3 to 6 cycles of neoadjuvant chemotherapy).
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Evaluation of the significance of baseline neutrophil lymphocyte ratio, platelet lymphocyte ratio, and CA 125 KELIM score in predicting surgical outcomes.
The success of the interval debulking surgery will be categorized based on the presence of residual tumor into complete cytoreduction (no macroscopically visible tumor) versus incomplete cytoreduction following neoadjuvant chemotherapy.
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At the time of interval debulking surgery (typically performed after 3 to 6 cycles of neoadjuvant chemotherapy).
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協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
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研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- Soh-Med-26-6-3MS
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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