2023-508724-35-00招募中2 期
TRIFLUOX-DP: Safety of Trifluridine/tipiracil as replacement of fluoropyrimidines (5-fluorouracil and capecitabine) based chemotherapy as first line metastatic colorectal or gastroesophageal cancer regimens in patients with dihydropyrimidine dehydrogenase deficiency: a phase II trial
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- Unicancer
- 入组人数
- 73
- 试验地点
- 21
- 主要终点
- The co-primary endpoint including: the rate of patients without specific toxicities defined as grade 3-4-5 digestive toxicities (diarrhoea and/or stomatitis) and grade 4-5 neutropenia or febrile neutropenia over the first 2 cycles (1 month of treatment) of first-line metastatic treatment (NCI CTCAE v5.0) AND the disease control rate after the 1st evaluation at 2 months of treatment.
研究概览
简要总结
To evaluate the specific safety and preliminary efficacy of an alternative chemotherapy option, namely Trifluridine/tipiracil, as replacement of 5FU- or capecitabine-based chemotherapy in pMMR/MSS metastatic colorectal or metastatic gastroesophageal adenocarcinomas first line regimens for patients with partial or complete DPD deficiency.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 years 至 65+ years（18-64 Years, 65+ Years）
- 接受健康志愿者
- 是
入选标准
- •Patient must have signed and dated a written informed consent form prior to any trial specific procedures. When the patient is physically unable to give their written consent, a trusted person of their choice, independent from the investigator or the sponsor, can confirm in writing the patient’s consent.
- •For women of reproductive potential, negative serum beta human chorionic gonadotropin (β- HCG) pregnancy test obtained within 7 days before the start of study treatment. Women not of reproductive potential are female patients who are postmenopausal or permanently sterilized (e.g., tubal occlusion, hysterectomy, bilateral salpingectomy)
- •For women of childbearing potential and men, agreement to use an adequate contraception for the duration of study participation and up to 7 months following completion of therapy
- •Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures
- •Affiliation to the Social Security System (or equivalent).
- •Histological or cytological documentation of proficient mismatch repair or microsatellite stable (pMMR/MSS) adenocarcinoma of the colon or rectum OR gastroesophageal cancer (lower oesophagus, gastroesophageal junction and gastric)
- •Unresectable synchronous or metachronous metastatic colorectal or gastroesophageal cancer
- •Presence of at least one measurable lesion according to RECIST v1.1
- •No prior therapy for metastatic disease
- •Known DPD deficiency defined as plasma uracil concentration≥16 ng/ml
- •Age ≥18 years
- •Eastern Cooperative Oncology Group (ECOG) performance status ≤1
- •Adequate bone marrow, renal, and liver functions as evidenced by the laboratory requirements within 7 days prior to study treatment initiation
排除标准
- •Previous or concurrent cancer that is distinct in primary site or histology from colorectal or gastroesophageal cancer within 5 years prior to study inclusion, except for curatively treated cervical cancer in situ, non-melanoma skin cancer and superficial bladder tumours [Ta (non invasive tumour), Tis (carcinoma in situ) and T1 (lamina propria invasion)]
- •Chronic hepatitis B or C infection (if hepatitis status cannot be obtained from medical records, re-testing is required)
- •Seizure disorder requiring medication
- •Symptomatic metastatic brain or meningeal tumours
- •History of organ allograft
- •Known hypersensitivity to any of the study drugs, study drug classes, or any constituent of the products
- •Use of live or live attenuated vaccines
- •Ongoing toxicities: a. Peripheral neuropathy >Grade 1 (NCI CTCAE v.5.0) b. Unresolved Grade 3 or 4 non-haematological clinically relevant toxicity from prior therapies
- •Hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption or any uncontrolled malabsorption condition
- •Inability to swallow oral medication
- •In case of planned treatment with nivolumab: a. Participant has received systemic steroid therapy (>10 mg daily prednisone or equivalent) or is receiving any other form of immunosuppressive medication. b. Active autoimmune disease or medical conditions requiring systemic immunosuppression that has required systemic treatment
- •Patients with colorectal cancer with high microsatellite instability (MSI-H) or mismatched repair disease (dMMR) tumor
- •In case of planned treatment with trastuzumab: a. a threshold value for the left ventricular ejection fraction (LVEF) measured at inclusion that does not allow treatment with trastuzumab (<55%), b. severe dyspnoea at rest due to complications of advanced malignancy or requiring supplementary oxygen therapy c. Known hypersensitivty to murine proteins
- •In case of planned treatment with bevacizumab: a. Proteinuria that does not allow treatment with bevacizumab, b. Pre-existing gastrointestinal or non-gastrointestinal fistula, c. Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to first dose of treatment d. Evidence or history of any bleeding diathesis, irrespective of severity. Any hemorrhage or bleeding event ≥CTCAE v 5.0 Grade 3 within 4 weeks prior to the start of study medication e. Prior arterial thromboembolic reactions, including cerebrovascular accidents, transient ischaemic attacks less than 12 months before first dose of bevacizumab f. Known hypersensitivity to Chinese Hamster Ovary (CHO) cell products or other recombinant human or humanized antibodies
- •In case of planned treatment with trastuzumab or panitumumab or bevacizumab: Interstitial lung disease with ongoing signs and symptoms
- •Pregnant or breast-feeding subjects. Women of childbearing potential must have a serum pregnancy test performed a maximum of 7 days before start of treatment, and a negative result must be documented before start of study drug
- •Patients unwilling or unable to comply with the medical follow-up required by the trial because of geographic, familial, social, substance abuse, medical or psychological reasons, or any condition that, in the opinion of the investigator, would interfere with the patient’s participation in the study or evaluation of study treatment or interpretation of patient safety or study results
- •Participation in another clinical study with an investigational product during the last 30 days before inclusion
- •Patients who might be interconnected with or dependent on the sponsor site or the investigator
- •Persons deprived of their liberty or under protective custody or guardianship, or legal incapacity or limited legal capacity
- •Patients with CPS≥1 HER2-positive gastroesophageal adenocarcinomas with planned treatment of pembrolizumab if access to pembrolizumab is available.
- •Patients with resectable metastases of colorectal cancer.
- •Radiotherapy within 28 days prior to first dose of treatment
- •Active cardiac disease or abnormal cardiac function including any of the following: a. QT/QTc interval longer than 450 msec for men and longer than 470 msec for women monitored by an ECG at inclusion b. Symptomatic Congestive heart failure ≥New York Heart Association (NYHA) class 3 or 4 c. Severe Unstable angina (angina symptoms at rest) d. Myocardial infarction less than 12 months before first dose of treatment
- •Uncontrolled hypertension (Systolic blood pressure ≥140 mmHg or diastolic pressure ≥ 90 mmHg) despite optimal medical management for treatement by bevacizumab
- •Ongoing infection ≥Grade 2 (NCI CTCAE v.5.0)
- •Known history of human immunodeficiency virus (HIV) infection
结局指标
主要结局
The co-primary endpoint including: the rate of patients without specific toxicities defined as grade 3-4-5 digestive toxicities (diarrhoea and/or stomatitis) and grade 4-5 neutropenia or febrile neutropenia over the first 2 cycles (1 month of treatment) of first-line metastatic treatment (NCI CTCAE v5.0) AND the disease control rate after the 1st evaluation at 2 months of treatment.
The co-primary endpoint including: the rate of patients without specific toxicities defined as grade 3-4-5 digestive toxicities (diarrhoea and/or stomatitis) and grade 4-5 neutropenia or febrile neutropenia over the first 2 cycles (1 month of treatment) of first-line metastatic treatment (NCI CTCAE v5.0) AND the disease control rate after the 1st evaluation at 2 months of treatment.
次要结局
- Safety of combination treatment (NCI CTCAE v5.0) determined through the incidence of adverse events, treatment-related adverse events, serious adverse events (SAE), and death; for the whole population and depending on glomerular filtration rate ([50-60[ vs [60- 90[ vs ≥90 mL/min per 1.73 m2)
- Dose intensity of combination treatment per patient and per cycle for cycle 1 and cycle 2 before third cycle
- Treatment efficacy : PFS, Overall survival, Objective response rate, Disease control rate
- Health-related quality of life will be assessed using the EORTC QLQ-C30 and EORTC QLQ-OG25 questionnaires for patients with gastroesophageal adenocarcinomas or EORTC QLQ-CR29 for patients with colorectal adenocarcinomas at baseline and every 2 months until disease progression and/or at least 3 months after study treatment stop
研究者
Nourredine AIT RAHMOUNE
Scientific
Unicancer
研究点 (21)
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