Phase Ib/II Trial of Serine/Glycine-Restricted Diet With Chemoradiotherapy for Rectal Cancer (SG-RCT)
Phase Ib/II Clinical Trial of Serine/Glycine-Restricted Diet Combined With Chemoradiotherapy for Neoadjuvant Treatment of Rectal Cancer
This is a Phase Ib/II seamless, open-label, clinical trial evaluating the safety and efficacy of a serine/glycine-restricted diet combined with neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer (LARC).
The study consists of two phases. Phase Ib is a non-randomized, single-arm safety run-in phase enrolling 6 patients, all of whom will receive the experimental regimen (a serine/glycine-restricted diet plus CAPOX chemotherapy and long-course radiotherapy). The primary objective of Phase Ib is to assess the safety, tolerability, and dietary compliance.
If the safety criteria are met in Phase Ib (≥3 grade diet-related adverse event rate ≤20% and compliance rate ≥70%), the study will proceed to Phase II. Phase II is a randomized, open-label, parallel-controlled phase in which 120 additional patients will be randomized in a 1:1 ratio to either the experimental group (serine/glycine-restricted diet plus standard neoadjuvant chemoradiotherapy) or the control group (standard neoadjuvant chemoradiotherapy alone). The total enrollment is 126 patients (6 in Phase Ib + 120 in Phase II).
The primary endpoint is the complete response rate (pCR + cCR). Secondary endpoints include major pathological response (MPR) rate, R0 resection rate, mrTRG regression grade, event-free survival (EFS), progression-free survival (PFS), overall survival (OS), adverse event profile, changes in serum amino acid levels, quality of life (EORTC QLQ-C30), and nutritional status. Exploratory endpoints include gut microbiome diversity and tumor immune microenvironment changes.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:Xuelei Ma, MD
- 電話番号:13408410416
- メール:drmaxuelei@gmail.com
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Written informed consent obtained prior to any study-related procedures.
- Male or female, aged 18-80 years.
- Histologically confirmed locally advanced mid-to-upper rectal cancer, staged as cT3, cT4, or node-positive by pelvic MRI.
- ECOG performance status score of 0 or 1.
- NRS-2002 score < 3.
- BMI ≥ 18.5 kg/m².
- Capable of oral intake or via feeding tube, and able to tolerate enteral nutrition.
- Adequate organ function meeting the following laboratory criteria:
ANC ≥ 1.5×10⁹/L (without G-CSF within 14 days);
Platelet count ≥ 100×10⁹/L;
Hemoglobin ≥ 9 g/dL (without transfusion or erythropoietin within 7 days);
Serum albumin ≥ 3.0 g/dL;
Total bilirubin ≤ 1.5× ULN;
AST and ALT ≤ 2.5× ULN;
Creatinine clearance ≥ 50 mL/min or serum creatinine ≤ 1.5× ULN;
INR ≤ 1.5× ULN, PT and APTT ≤ 1.5× ULN;
Urine protein < 2+;
Cardiac enzymes within normal range.
- Female patients of childbearing potential must have a negative serum pregnancy test within 3 days prior to study treatment and agree to use highly effective contraception for at least 6 months after the last dose.
- All patients at risk of pregnancy must use highly effective contraceptive methods during the treatment period and up to 120 days (or 180 days after last chemotherapy dose) after the last dose of study treatment.
Exclusion Criteria:
- Stage I or Stage IV rectal cancer.
- Cognitive impairment or psychiatric disorders preventing comprehension of the study content.
- Central nervous system or meningeal metastases.
- Clinically symptomatic moderate to severe ascites requiring therapeutic paracentesis.
- Uncontrolled or moderate to severe pleural effusion and pericardial effusion.
- Severe diarrhea, intractable vomiting, severe malabsorption syndrome, paralytic or mechanical intestinal obstruction; tracheoesophageal fistula, gastrointestinal perforation or fistula, intra-abdominal abscess; gastrointestinal bleeding (CTCAE grade ≥ 3 within 6 months or grade ≥ 2 within 3 months before study treatment).
- Any other condition that may affect the study results or lead to forced discontinuation as judged by the investigator (e.g., alcohol or drug abuse, serious concurrent diseases, severe laboratory abnormalities).
- Known allergy to the study drugs or nutritional powder active ingredients or excipients.
- Poorly controlled diabetes mellitus.
- Severe cardiovascular/cerebrovascular diseases, including CVA, TIA, myocardial infarction, major vascular disease within 6 months; uncontrolled symptomatic cardiac disease (e.g., unstable angina, NYHA class II or higher heart failure, LVEF < 50% on echocardiography, or severe uncontrolled arrhythmia).
- Pregnant or lactating women.
- Any other condition that the investigator considers unsuitable for enrollment.
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
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:Serine/Glycine-Restricted Diet Plus Chemoradiotherapy
|
A specialized liquid nutritional powder free of serine and glycine, supplemented with a specified list of low-serine/glycine foods. Patients receive 30 kcal/kg/day energy and 1.5 g/kg/day protein for 7-8 weeks during the neoadjuvant treatment period. Oxaliplatin and capecitabine combination chemotherapy administered for 6 cycles as part of the standard neoadjuvant regimen. Pelvic radiotherapy delivered with a total dose of 45.0-50.4 Gy in 25-28 fractions, concurrent with capecitabine. |
|
アクティブコンパレータ:Standard Chemoradiotherapy Without Dietary Restriction
|
Oxaliplatin and capecitabine combination chemotherapy administered for 6 cycles as part of the standard neoadjuvant regimen. Pelvic radiotherapy delivered with a total dose of 45.0-50.4 Gy in 25-28 fractions, concurrent with capecitabine. |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Rate of Complete Response (Pathological and Clinical)
時間枠:At the time of radical surgery (approximately 24 weeks after initiation of neoadjuvant treatment), or at the time of clinical evaluation for cCR (if patients opt for a Watch-and-Wait strategy).
|
The proportion of patients achieving pathological complete response (pCR) or clinical complete response (cCR). pCR is defined as no residual tumor cells in the resected tumor and regional lymph nodes. cCR is defined as no evidence of residual tumor in the primary lesion and regional lymph nodes after neoadjuvant therapy, assessed by digital rectal examination, endoscopy, pelvic high-resolution MRI (T2WI/DWI), and serum CEA levels. |
At the time of radical surgery (approximately 24 weeks after initiation of neoadjuvant treatment), or at the time of clinical evaluation for cCR (if patients opt for a Watch-and-Wait strategy).
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- Approval No. 1646 (2026)
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?
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
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