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

4 września 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Rekrutacyjny

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Szacowany)

15

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Sichuan
      • Chengdu, Sichuan, Chiny, 610041
        • Rekrutacyjny
        • West China Hospital
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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.
Kohorta z niską dawką: 100 mg QD, wykonana przed pierwszym posiłkiem dnia. Kohorta wysokiej dawki: dawka początkowa 100 mg QD przez 1 tydzień. W przypadku tolerowanej dawka eskaluje do 300 mg QD, zabranego przed pierwszym posiłkiem dnia.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Number of Participants With Treatment-Emergent Adverse Events as Assessed by CTCAE v5.0
Ramy czasowe: 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

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Overall survival
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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.

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Percentage of Prescribed Canagliflozin Doses Taken During Study Treatment
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

10 września 2026

Zakończenie podstawowe (Szacowany)

31 lipca 2028

Ukończenie studiów (Szacowany)

31 lipca 2028

Daty rejestracji na studia

Pierwszy przesłany

23 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

8 lipca 2026

Pierwszy wysłany (Rzeczywisty)

14 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 września 2026

Ostatnia weryfikacja

1 września 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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