- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT01490866
A Trial of Single Agent Axitinib as Maintenance Therapy for Patients With First Line Metastatic Colorectal Cancer (mCRC)
A Phase II Trial of Single Agent Axitinib as Maintenance Therapy for Patients With First Line Metastatic Colorectal Cancer (mCRC)
Обзор исследования
Статус
Условия
Подробное описание
Тип исследования
Регистрация (Действительный)
Фаза
- Фаза 2
Контакты и местонахождение
Места учебы
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Arkansas
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Jonesboro, Arkansas, Соединенные Штаты, 72401
- NEA Baptist Clinic
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Florida
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Fort Myers, Florida, Соединенные Штаты, 33916
- Florida Cancer Specialists-South
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Pensacola, Florida, Соединенные Штаты, 32503
- Woodlands Medical Specialists
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Saint Petersburg, Florida, Соединенные Штаты, 33705
- Florida Cancer Specialists-North
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Georgia
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Gainesville, Georgia, Соединенные Штаты, 30501
- Northeast Georgia Medical Center
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Indiana
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Newburgh, Indiana, Соединенные Штаты, 47630
- Oncology Hematology of SW Indiana
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Terre Haute, Indiana, Соединенные Штаты, 47802
- Hope Cancer Center
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Michigan
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Grand Rapids, Michigan, Соединенные Штаты, 49503
- Grand Rapids Oncology Program
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Nebraska
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Omaha, Nebraska, Соединенные Штаты, 68114
- Nebraska Methodist Hospital
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New Jersey
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Summit, New Jersey, Соединенные Штаты, 07901
- Atlantic Health System
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Tennessee
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Nashville, Tennessee, Соединенные Штаты, 37203
- Tennessee Oncology
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Texas
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Dallas, Texas, Соединенные Штаты, 75243
- Texas Health Physician Group
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
- Histologically or cytologically confirmed metastatic adenocarcinoma of the colon or rectum.
- Patients must have measurable disease per RECIST Version 1.1.
- No previous systemic therapy for metastatic colorectal cancer. Previous radiosensitizing chemotherapy is allowed, if completed at least 4 weeks prior to Cycle 1 Day 1 of study treatment, and previous neoadjuvant and/or adjuvant chemotherapy is allowed, if completed at least 6 months prior to diagnosis of metastatic disease.
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 to 1.
- Life expectancy >=12 weeks.
- Adequate hematologic, renal and hepatic function
- Patients who are on coumadin should have an INR value within the therapeutic range (i.e., 2 to 3 x ULN). Patients who are on stable, chronic doses of coumadin are eligible.
- Male patients willing to use adequate contraceptive measures. Female patients who are not of child-bearing potential, and female patients of child-bearing potential who agree to use adequate contraceptive measures, who are not breastfeeding, and who have a negative serum or urine pregnancy test performed within 72 hours prior to start of treatment.
- Willingness and ability to comply with the trial and follow-up procedures.
- Ability to understand the investigative nature of this trial and give written informed consent.
Exclusion Criteria:
- History or known presence of central nervous system (CNS) metastases.
- Patients who have had a major surgical procedure (not including mediastinoscopy), or significant traumatic injury <=4 weeks prior to beginning treatment.
- Women who are pregnant or lactating. All females of child-bearing potential must have negative serum or urine pregnancy tests within 72 hours prior to study treatment (see Appendix D)
- History of hypersensitivity to active or inactive excipients of any component of treatment (5 fluorouracil, bevacizumab, oxaliplatin, or axitinib), or known dipyrimidine dehydrogenase deficiency.
Patients with proteinuria at screening as demonstrated by:
- Urine dipstick for proteinuria >=2+ (patients discovered to have >=2+ proteinuria on dipstick urinalysis at baseline should undergo a 24-hour urine collection, and must demonstrate <=1 g of protein/24 hours to be eligible)
- Patients with a serious non healing wound, active ulcer, or untreated bone fracture.
- Patients with evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation).
- Patients with history of hematemesis or hemoptysis (defined as having bright red blood of ½ teaspoon or more per episode) <=1 month prior to study enrollment.
- Patients requiring concomitant treatment with potent CYP3A4 or CYP1A2 inducers and CYP3A4 inhibitors.
- History of myocardial infarction or unstable angina <=6 months prior to beginning treatment.
- Inadequately controlled hypertension (defined as systolic blood pressure >150 mmHg and/or diastolic blood pressure >100 mmHg while on antihypertensive medications). Initiation of antihypertensive agents is permitted provided adequate control is documented at least 1 week prior to Day 1 of study treatment.
- New York Heart Association Grade II or greater congestive heart failure.
- Serious cardiac arrhythmia requiring medication. Patients with chronic, rate-controlled atrial fibrillation are eligible.
- Significant vascular disease (e.g., aortic aneurysm requiring surgical repair, or recent peripheral arterial thrombosis) <=6 months prior to Day 1 of treatment.
- History of stroke or transient ischemic attack <=6 months prior to beginning treatment.
- Any prior history of hypertensive crisis or hypertensive encephalopathy.
- History of abdominal fistula or gastrointestinal perforation <=6 months prior to Day 1 of beginning treatment.
- Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
- Any known positive test for human immunodeficiency virus, hepatitis C virus or acute or chronic hepatitis B infection.
- Mental condition that would prevent patient comprehension of the nature of, and risk associated with, the study.
- Use of any non-approved or investigational agent <=28 days prior to administration of the first dose of study drug. Patients may not receive any other investigational or anti-cancer treatments while participating in this study.
- Past or current history of neoplasm other than the entry diagnosis with the exception of treated non-melanoma skin cancer or carcinoma in situ of the cervix, or other cancers cured by local therapy alone and a disease free survival >=5 years.
- Infection requiring IV antibiotics.
- Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter drug absorption (e.g. active inflammatory bowel disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or significant small bowel resection).
- Inability to swallow whole tablets.
- Patients with > Grade 2 peripheral neuropathy.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Н/Д
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: FOLFOX/bevacizumab and Axitinib
Phase II trial investigating axitinib as a single-agent maintenance therapy following standard first-line FOLFOX/bevacizumab therapy for patients with mCRC. (FOLFOX is a combination of 5-Fluorouracil, Leucovorin and Oxaliplatin.) All patients will receive FOLFOX/bevacizumab for four 28-day cycles (a total of 16 weeks). After 4 cycles, maintenance axitinib will be started. |
5-mg tablets PO BID
Другие имена:
5 mg/kg Days 1 and 15; IV
Другие имена:
400 mg/m2 Days 1 and 15; IV
Другие имена:
2400 mg/m2 over 46-48 hours Days 1 and 15; Continuous Intravenous
Другие имена:
400 mg/m2 Days 1 and 15; IV
Другие имена:
85 mg/m2 Days 1 and 15; IV
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Progression-free Survival
Временное ограничение: 24 months
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Defined as the time from first treatment until objective tumor progression or death from any cause, assessed according to Response Evaluation Criteria for Solid Tumors (RECIST) v1.1.
|
24 months
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Objective Response Rate
Временное ограничение: every 8 weeks, assessed up to approximately 24 months
|
Defined as the percentage of evaluable patients showing a complete or partial response (CR or PR) per RECIST v1.1 criteria.
CR = disappearance of all lesions.
PR = at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
Stable disease (SD) = neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest (nadir) sum LD since start of treatment.
|
every 8 weeks, assessed up to approximately 24 months
|
|
Time To Progression (TTP)
Временное ограничение: every 8 weeks, assessed approximately up to 24 months
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Defined as the time after a disease is diagnosed (or treated) until worsening of the disease.
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every 8 weeks, assessed approximately up to 24 months
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Overall Survival (OS)
Временное ограничение: every 8 weeks until progression then every 3 months for up to 5 years.
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Defined as the time from first treatment until death from any cause.
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every 8 weeks until progression then every 3 months for up to 5 years.
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|
Frequency of Adverse Events as a Measure of Safety
Временное ограничение: Every 4 weeks plus 30 days during treatment and up to 5 years thereafter.
|
The frequency of adverse events (AEs) was analyzed in 2 groups of patients, those receiving FOLFOX/bevacizumab (N=70), and patients who received axitinib maintenance (N = 48).
AEs were assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0.
|
Every 4 weeks plus 30 days during treatment and up to 5 years thereafter.
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Соавторы и исследователи
Соавторы
Следователи
- Учебный стул: Johanna Bendell, M.D., SCRI Development Innovations, LLC
Даты записи исследования
Изучение основных дат
Начало исследования
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Оценивать)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Заболевания пищеварительной системы
- Новообразования
- Новообразования по локализации
- Желудочно-кишечные новообразования
- Новообразования пищеварительной системы
- Желудочно-кишечные заболевания
- Заболевания толстой кишки
- Кишечные заболевания
- Новообразования кишечника
- Заболевания прямой кишки
- Колоректальные новообразования
- Физиологические эффекты лекарств
- Молекулярные механизмы фармакологического действия
- Ингибиторы ферментов
- Антиметаболиты, Противоопухолевые
- Антиметаболиты
- Противоопухолевые агенты
- Иммунодепрессанты
- Иммунологические факторы
- Защитные агенты
- Противоопухолевые агенты, иммунологические
- Ингибиторы ангиогенеза
- Агенты, модулирующие ангиогенез
- Вещества роста
- Ингибиторы роста
- Микроэлементы
- Ингибиторы протеинкиназы
- Витамины
- Противоядия
- Комплекс витаминов группы В
- Фторурацил
- Оксалиплатин
- Бевацизумаб
- Лейковорин
- Акситиниб
Другие идентификационные номера исследования
- SCRI GI 154
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .