TEMPLE - Thiopurine Enhanced Mutations for PD-1/Ligand-1 Efficacy
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Adverse events
研究概览
简要总结
The TEMPLE study is a single-center prospective phase Ib and II trial to determine the safety, tolerability and efficacy of Atezolizumab given in combination with thiopurine therapy (6-mercaptopurine and 6-thioguanine) in patients with advanced and/or metastatic solid tumors with an intermediate tumor mutational burden.
Maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D) will be determined in a single armed, open label phase Ib trial with a fixed dose of Atezolizumab in combination with thiopurine therapy with a dose-limiting toxicity (DLT) period of 4 weeks. A total of 27-39 patients will be enrolled in the TEMPLE study. Phase Ib will enroll 3-18 patients depending on the number of DLTs and need for dose de-escalation. Data from patients treated in the phase Ib study at RP2D will be included when assessing endpoints in the phase II part of the study. Phase II will enroll a total of 27 patients (including 3-6 patients treated at RP2D in the phase I part of the trial) in a Simon's 2 stage design (13 in stage 1 and 14 in stage 2).
详细描述
INTRODUCTION:
Immune checkpoint inhibitors (ICI) have revolutionized treatment of several cancer types. However, many patients fail to respond. A prerequisite for response is the presence of neoepitopes on cancer cells that trigger the immune system, and the likelihood hereof increases with the number of mutations in the cancer. The thiopurines 6-mercaptopurine (6MP) and 6-thioguanine (6TG) are prodrugs that are converted into cytotoxic metabolites that are incorporated into DNA (DNA-TG) and cause DNA-damage through futile DNA mismatch repair attempts. 6MP and 6TG have been used for more than 50 years for long-term treatment of hematological cancers. In leukemia, high levels of DNA-TG are associated with higher cure rates. A recent pilot study has shown that combination therapy with 6MP and 6TG significantly increases DNA-TG levels and that the drug combination is safe and tolerable. The higher DNA-TG levels most likely increase the mutational burden and thus presence of neoepitopes that activate cytotoxic T-cell responses.
The TEMPLE project will apply the innovative thiopurine combination strategy to increase the mutational burden, presence of neoepitopes and thus proportion of patients with incurable solid cancers that respond to treatment with ICIs.
STUDY DESIGN:
The TEMPLE study is a single-center prospective phase Ib and II trial to determine the safety, tolerability and efficacy of Atezolizumab given in combination with thiopurine therapy in patients with advanced and/or metastatic solid tumors with an intermediate tumor mutational burden. Maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D) will be determined in a single armed, open label phase Ib trial with a fixed dose of Atezolizumab in combination with thiopurine therapy. In the phase Ib part of the study, patients will start treatment with investigational medicinal products:
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The patient MUST MEET ALL the following criteria to be enrolled in the study:
- •Signed written informed consent.
- •Age ≥ 18 years.
- •Performance status (WHO) of 0-
- •Histologically confirmed advanced and/or metastatic solid tumors for which standard curative measures do not exist.
- •Radiologically measurable disease according to RECIST v1.
- •Life expectancy estimated by the Investigator to be ≥12 weeks.
- •Metastatic Lesion(s) or primary tumour accessible for biopsy
- •Intermediate tumor mutational burden of 5-10 mutations/mb
- •Adequate organ function assessed by screening laboratory values:
- •Absolute lymphocyte count ≥ 0.5 x 109/L
- •Neutrophils ≥ 1.5 x 109/L
- •Platelets ≥ 100 x 109/L. For patients with primary hepatocellular carcinoma platelet counts ≥65 x 109/L is allowed.
- •Hemoglobin ≥ 90 g/L (5.6 mmol/L) and at least 4 weeks since blood transfusion
- •Serum creatinine ≤ 1.5 × upper limit of normal (ULN) or calculated by Cockroft-Gault formula or directly measured creatinine clearance ≥ 50 mL/min at screening
- •AST ≤ 3 x ULN without, and ≤ 5 x ULN with hepatic metastasis
- •Bilirubin ≤ 1.5 x ULN (except patients with Gilbert's syndrome, who must have total bilirubin < 3.0 mg/dL)
- •Ability to take oral medications.
- •Woman of childbearing potential must have been tested negative in a serum pregnancy test within 5 days prior to study drug initiation.
- •Male and female patients who have the potential to reproduce must agree to use a highly effective method of birth control (i.e., pregnancy rate of less than 1 % per year) during the study and for 5 months after the discontinuation of study medication. Women must refrain from donating eggs and men must refrain from donating sperm during this same period.
排除标准
- •Any of the following :
- •Pregnancy, lactation, or breastfeeding.
- •History or clinical evidence of central nervous system (CNS) primary tumors or metastases including leptomeningeal metastases, unless they have been previously treated, are asymptomatic, and have had no requirement for steroids or anticonvulsants in the last 14 days prior to Screening.
- •Deficiency in thiopurine methyltransferase (TPMT) or NUDT
- •Use, or have used, any concomitant anti-cancer medications within the previous 30 days or 5 half-lives of the medication (whichever is shortest) prior to first dose (bisphosphonates, denosumab and androgen deprivation therapies such as LHRH (GnRH) agonists are allowed if patient is on stable treatment for at least 4 weeks prior to first dose). Limited field radiotherapy for palliative purpose is allowed at any time.
- •Participants with immune-related adverse events attributed to prior immunomodulatory therapy must have resolved to Grade ≤ 1 (according to NCI CTCAE v 5.0) or baseline other than adverse events that are clinically non-significant and/or stable on supportive therapy, and are not expected to interfere with treatment in the study such as:
- •Grade ≤ 2 alopecia, asthenia, dermatologic events.
- •Grade ≤ 2 anemia if hemoglobin ≥ 90 g/L (5.6 mmol/L)
- •Grade 2 (> 1.5-2.0 x ULN) asymptomatic amylase and/or lipase elevation with no abdominal pain and no characteristic CT findings. However, weekly monitoring of amylase and lipase is required in this case.
- •Be an organ transplant recipient.
- •Have a history of prior other malignancy (with the exception of localized prostate cancer, adequately treated basal skin cancer or carcinoma in-situ of the cervix) within 2 years prior to first dose.
- •Have a severe autoimmune disorder requiring treatment during the last 12 months prior to first dose. Diabetes on stable anti-diabetic medication, hypothyroidism and adrenocortical deficiency on stable substitution therapy are allowed.
- •Be on chronic therapy with systemic immunosuppressant medication (inhaled, intra articular and low dose systemic corticosteroids, e.g. 7.5 mg or less prednisolone per day is allowed, provided that treatment has been unchanged for at least 4 weeks prior to first dose of IMP).
- •Known HIV, active hepatitis B or hepatitis C infection.
- •Participants with a history of severe allergic anaphylactic reactions to chimeric or humanized antibodies or known hypersensitivity to Chinese hamster ovary cell products or to any component of the Atezolizumab formulation
- •Any condition that, in the opinion of the Investigator, would place the patient at increased risk or preclude the patient's compliance with the study.
研究组 & 干预措施
TEMPLE
Study drugs: Atezolizumab, 6-mercaptopurine and 6-thioguanine
干预措施: Atezolizumab, 6-mercaptopurine, 6-thioguanine (Combination Product)
结局指标
主要结局
Adverse events
时间窗: 3-6 months
Type and number of adverse events
Best overall response
时间窗: One year
Complete response (CR), partial response (PR), stable disease (SD), progressive disease (PD), unconfirmed (iUPD) and confirmed PD (iCPD), assessed according to Response Evaluation Criteria in Solid Tumours (RECIST) 1.1
Dose limiting toxicities
时间窗: 28 days
Dose limiting toxicities (DLTs) and the MTD for determination of RP2D of Atezolizumab, 6TG and 6MP
次要结局
- Duration of response(Two years)
- Progression Free Survival(Two years)
- Overall Survival(Two years)
研究者
Kristoffer Rohrberg
Sponsor- investigator
Rigshospitalet, Denmark