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Safety and Efficacy of Canagliflozin in Patients With Locally Advanced or Advanced Solid Cancer (SGLT2SOLID)

2026年9月4日 更新者:Xuelei Ma MD、West China Hospital

**Revised version:**

Locally advanced or advanced solid tumors remain a major clinical challenge despite multimodal treatments, including surgery, radiotherapy, chemotherapy, targeted therapy, and immunotherapy. For patients with unresectable, recurrent, metastatic, or treatment-refractory disease, prognosis remains poor, and effective therapeutic strategies are still urgently needed. Immune checkpoint inhibitors (ICIs), particularly PD-1/PD-L1 blockade, have transformed the treatment landscape of multiple solid tumors by reinvigorating anti-tumor immune responses through inhibition of the PD-1/PD-L1 pathway. However, only a subset of patients derive durable benefit from immunotherapy, and primary or acquired resistance remains common, highlighting the need for rational combination strategies to enhance anti-tumor efficacy.

Intriguingly, sodium-glucose cotransporter 2 inhibitors, originally developed as anti-diabetic agents, have shown emerging anti-tumor potential through metabolic regulation and modulation of the tumor microenvironment. In particular, combining SGLT-2 inhibition with immune checkpoint blockade may enhance tumor control through metabolic-immunologic crosstalk. Preclinical evidence suggests that the SGLT-2 inhibitor canagliflozin may suppress tumor growth and potentially improve the efficacy of PD-1 blockade. Based on this rationale, this phase I trial investigates the safety and efficacy of canagliflozin combined with tislelizumab in patients with locally advanced or advanced solid tumors, evaluating its impact on progression-free survival, overall survival, objective response rate, and tumor microenvironment modulation. This study aims to explore a novel metabolic-immunotherapy strategy based on dual metabolic and immune regulation, potentially providing a new therapeutic option for patients with locally advanced or advanced solid tumors.

調査の概要

状態

募集

研究の種類

介入

入学 (推定)

15

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Sichuan
      • Chengdu、Sichuan、中国、610041
        • 募集
        • West China Hospital
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

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

いいえ

説明

Inclusion Criteria:

  1. Aged ≥18 years and ≤80 years old at the time of signing the written informed consent form, regardless of gender.
  2. Patients with histologically or cytologically confirmed locally advanced or advanced solid tumors, including:

    1. Patients with unresectable locally advanced, recurrent, or distant metastatic solid tumors.
    2. Patients who have failed, are intolerant to, or are unsuitable for standard therapy, or for whom no standard therapy is available.
    3. Patients considered suitable for treatment with tislelizumab-based immunotherapy by the investigator.
  3. According to the Response Evaluation Criteria in Solid Tumors (RECIST 1.1), patients must have at least one target lesion with measurable diameters (tumor lesions with a long diameter ≥10 mm on CT scan, lymph node lesions with a short diameter ≥10 mm on CT scan, and a scan slice thickness of no more than 5 mm). Lesions that have received local treatments such as radiotherapy can be used as target lesions after clear progression is confirmed.
  4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 1, with an expected survival period of ≥3 months.
  5. Patients must be type 2 diabetes mellitus (T2DM) patients and meet the indications for canagliflozin; or patients have no diagnosis of diabetes, no history of type 1 diabetes or diabetic ketoacidosis.

    The diagnosis of type 2 diabetes mellitus is defined as typical diabetic symptoms plus random blood glucose ≥11.1 mmol/L, or plus fasting blood glucose ≥7.0 mmol/L, or plus 2-hour post-load blood glucose in oral glucose tolerance test (OGTT) ≥11.1 mmol/L, or plus HbA1c ≥6.5%. For those without typical diabetic symptoms, reexamination on another day is required for confirmation (excluding random blood glucose).

  6. Good function of major organs, that is, the relevant examination indicators within 14 days before randomization meet the following requirements (without blood or blood product transfusion, without the use of hematopoietic stimulating factors, and without the use of albumin or blood products):

    • Routine blood test: Hemoglobin ≥80 g/L; neutrophil count >1.5×10⁹/L; platelet count ≥90×10⁹/L.
    • Biochemical test: Total bilirubin ≤1.5×ULN (upper limit of normal value); serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤2.5×ULN; serum creatinine (SCr) ≤1.5×ULN or creatinine clearance rate ≥50 mL/min (Cockcroft-Gault formula).
    • Prothrombin time (PT), international normalized ratio (INR) ≤1.5×ULN (unless warfarin anticoagulation is being used).
    • Cardiac Doppler ultrasound evaluation: Left ventricular ejection fraction (LVEF) ≥50%.
    • Renal function: eGFR ≥60 mL/min/1.73 m².
    • Blood glucose: HbA1c ≤9%.
  7. Patients of childbearing potential (both male and female) must use effective medical contraceptive measures during the study period and within 6 months after the end of drug administration.
  8. Body mass index (BMI) ≥18.5 kg/m² during the study screening period.
  9. If complicated with hypertension, blood pressure must be controlled to a stable level with other medications.
  10. No history of peripheral vascular disease, neuropathy, or diabetic foot ulcers.
  11. Patients voluntarily join this study, sign the informed consent form, have good compliance, and patients and their families agree to cooperate with survival follow-up.

Exclusion Criteria:

  1. Participation in other drug clinical trials within 4 weeks.
  2. History of other tumors, except for in-situ cervical cancer, treated cutaneous squamous cell carcinoma, bladder epithelial tumors, or other malignant tumors that have received radical treatment (at least 5 years prior to enrollment).
  3. Patients with symptomatic or rapidly progressive central nervous system metastases, extensive lung metastases causing dyspnea, or tumors approaching or invading major blood vessels or nerves.
  4. Uncontrolled cardiac clinical symptoms or diseases, such as heart failure of NYHA class 2 or above, unstable angina, myocardial infarction within 1 year, or clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention.
  5. Pregnant or lactating women.
  6. Patients with active tuberculosis, bacterial or fungal infections (≥ grade 2, based on NCI-CTCAE 5.0), or HIV infection.
  7. Patients with a history of psychoactive drug abuse that cannot be 戒除 (abstained from) or with mental disorders.
  8. Subjects with any active autoimmune diseases or a history of autoimmune diseases (including but not limited to: uveitis, enteritis, hypophysitis, nephritis, hyperthyroidism, hypothyroidism; subjects with vitiligo or childhood asthma that has fully remitted and requires no intervention in adulthood may be included; subjects with asthma requiring medical intervention with bronchodilators shall not be included).
  9. Previous treatment with SGLT2 inhibitors (such as dapagliflozin, empagliflozin, canagliflozin).
  10. Long-term steroid use or combined use of insulin/insulin sensitizers.
  11. Baseline HbA1c >10%, history of stroke or transient ischemic attack within 5 years, and uncontrolled comorbidities.
  12. Female subjects with a pregnancy plan or male subjects whose partners have a pregnancy plan from the screening period to 12 months after medication.
  13. Patients with primary peritoneal carcinoma.
  14. Patients with type 1 diabetes or diabetic ketoacidosis.
  15. History of peripheral vascular disease, neuropathy, or diabetic foot ulcers.
  16. Patients with severe renal insufficiency (eGFR <30 mL/min/1.73 m²).
  17. Patients with recurrent genitourinary infections within six months or requiring long-term anti-infective treatment.
  18. Patients with a history of lower limb amputation, severe peripheral vascular disease, or neuropathy.
  19. Patients with uncontrolled hypothyroidism.
  20. Other conditions deemed unsuitable for enrollment by the investigator.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Intervention group
Canagliflozin: According to the drug's prescribing information, the recommended starting dose is 100 mg once daily (qd), taken orally before the first meal of the day. For patients who tolerate 100 mg qd and have an estimated glomerular filtration rate (eGFR) ≥60 ml/min/1.73 m² with a need for additional glycemic control, the dose may be increased to 300 mg qd. In this study's dose-escalation phase, two dose levels will be evaluated: Low-dose cohort: 100 mg qd, taken before the first meal of the day. High-dose cohort: Starting dose of 100 mg qd for 1 week. If tolerated, the dose will escalate to 300 mg qd, taken before the first meal of the day.
低用量コホート:100 mg QD、その日の最初の食事の前に撮影。 高用量コホート:1週間の100 mg QDの開始用量。 許容されると、その日の最初の食事の前に採取された300 mg QDに線量がエスカレートします。

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
Number of Participants With Treatment-Emergent Adverse Events as Assessed by CTCAE v5.0
時間枠:Through study completion, an average of 1 year
Treatment-emergent adverse events will be assessed and summarized by number and percentage of participants, severity, seriousness, and relationship to study treatment.
Through study completion, an average of 1 year

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall survival
時間枠:From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Overall survival is defined as the time from the date of randomization to the date of death from any cause.
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Progression-Free Survival (PFS)
時間枠:From date of randomization until the date of first documented disease progression or death from any cause, whichever occurs first, assessed up to 100 months
Progression-free survival is defined as the time from the date of randomization to the date of first documented disease progression or death from any cause, whichever occurs first.
From date of randomization until the date of first documented disease progression or death from any cause, whichever occurs first, assessed up to 100 months
Immunogenicity assessment
時間枠:through study completion, an average of 1 year
Flow cytometry will be used to assess CD8+ T-cell function, proliferation, and polyfunctional T-cell subsets. Changes from baseline will be summarized descriptively.
through study completion, an average of 1 year
Gut Microbiome Metagenomic Profiling
時間枠:From baseline to treatment discontinuation, disease progression, death, or completion of study treatment, whichever occurs first.
Gut microbiome composition and functional profiles will be assessed using metagenomic sequencing of fecal samples. Exploratory analyses will include microbial diversity, relative abundance of key bacterial taxa, microbial functional pathways, and their association with treatment response, disease progression, and treatment-related adverse events.
From baseline to treatment discontinuation, disease progression, death, or completion of study treatment, whichever occurs first.

その他の成果指標

結果測定
メジャーの説明
時間枠
Percentage of Prescribed Canagliflozin Doses Taken During Study Treatment
時間枠:From initiation of canagliflozin treatment through treatment discontinuation or completion of study treatment, up to 1 year
Medication adherence will be assessed as the proportion of prescribed canagliflozin doses actually taken during the treatment period. Adherence will be calculated based on drug accountability records, patient diaries, and/or returned tablets, and summarized as a percentage for each participant and overall.
From initiation of canagliflozin treatment through treatment discontinuation or completion of study treatment, up to 1 year
Change From Baseline in Blood Glucose Levels During Study Treatment
時間枠:From baseline until treatment discontinuation, disease progression, death, withdrawal of consent, or completion of study treatment, whichever occurs first.
Blood glucose levels will be assessed during the study to evaluate metabolic changes associated with canagliflozin treatment. Changes from baseline in fasting blood glucose and/or random blood glucose will be summarized descriptively, and abnormal glucose-related events, including hypoglycemia or hyperglycemia, will be recorded when applicable.
From baseline until treatment discontinuation, disease progression, death, withdrawal of consent, or completion of study treatment, whichever occurs first.
Change From Baseline in Hemoglobin Levels During Study Treatment
時間枠:Baseline and during study treatment, up to 1 year
Hemoglobin levels will be assessed during the study as part of hematologic safety monitoring. Changes from baseline in hemoglobin levels will be summarized descriptively, and clinically significant decreases in hemoglobin or anemia-related events will be recorded when applicable.
Baseline and during study treatment, up to 1 year

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月10日

一次修了 (推定)

2028年7月31日

研究の完了 (推定)

2028年7月31日

試験登録日

最初に提出

2026年6月23日

QC基準を満たした最初の提出物

2026年7月8日

最初の投稿 (実際)

2026年7月14日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月9日

QC基準を満たした最後の更新が送信されました

2026年9月4日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

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?

いいえ

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

いいえ

米国FDA規制機器製品の研究

いいえ

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