Sintilimab Versus Mitomycin in Combination With Capecitabine and IMRT for Limited-stage Anal Squamous Cell Carcinoma
A Multicenter, Phase III, Randomized Controlled Clinical Trial of Sintilimab Versus Mitomycin in Combination With Capecitabine and Intensity-Modulated Radiotherapy in the Treatment of Limited-stage Anal Squamous Cell Carcinoma
Обзор исследования
Статус
Статус
Условия
Условия
Вмешательство/лечение
Вмешательство/лечение
Тип исследования
Тип исследования
Регистрация (Оцененный)
Регистрация
Фаза
Фаза
- Фаза 3
Контакты и местонахождение
Контакты исследования
Контакты исследования
- Имя: Yangmei Zhou, MD, PhD
- Номер телефона: +86 0755-66618168-51251
- Электронная почта: szchiec@163.com
Учебное резервное копирование контактов
- Имя: Yuan Tang, MD, PhD
- Номер телефона: +86-15011304945
- Электронная почта: tangyuan82@126.com
Места учебы
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Beijing Municipality
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Beijing, Beijing Municipality, Китай, 100021
- Рекрутинг
- National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
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Контакт:
- Yuan Tang, MD, PhD
- Номер телефона: +86-15011304945
- Электронная почта: tangyuan82@126.com
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Guangdong
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Shenzhen, Guangdong, Китай
- Рекрутинг
- National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen
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Контакт:
- Yangmei Zhou, MD, PHD
- Номер телефона: +86-0755-66618168-51251
- Электронная почта: szchiec@163.com
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Критерии участия
Критерии приемлемости
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Histopathologically confirmed primary anal squamous cell carcinoma, including a subset of rectal squamous cell carcinomas. Definition for inclusion of rectal squamous cell carcinomas: According to Williams' criteria (1979) and WHO classification (2019), rectal squamous cell carcinomas included in this study must meet all of the following criteria: (1) Histopathologically confirmed as pure squamous cell carcinoma, excluding adenosquamous carcinoma; (2) Digital examination/endoscopy/MRI confirmation that the tumor mass is entirely located in the rectum (above the dentate line), with no evidence of primary origin in the anal canal or upward spread. If the inferior border of the tumor is within 5-6 cm from the anal verge, and the patient is scheduled to undergo radical radiotherapy and chemotherapy, the rectal squamous cell carcinoma can be diagnosed and screened for inclusion (When the primary epicenter cannot be determined, regardless of which side the tumor mass is biased towards, the diagnosis shall be considered for screening and inclusion as anal squamous cell carcinoma); (3) Female patients must be excluded for rectal metastasis from cervical squamous cell carcinoma (baseline gynecological examination is recommended).
- Staged as cT2-T4N0M0 or cTanyN+M0 by imaging (AJCC 9th).
- No prior tumor resection surgery (other than biopsy) or chemotherapy or other anti-tumor therapy.
- Aged 18-75 years old.
- ECOG performance status of 0-1.
- Adequate organ function reserve: white blood cell (WBC) count ≥3 × 10^9/L, absolute neutrophil count (ANC) ≥1.5 × 10^9/L, hemoglobin (Hb) level >90 g/L, platelet (PLT) count >100 × 10^9/L; serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels <2.5 times the upper limit of normal (ULN); serum bilirubin level ≤1.5 × ULN; serum creatinine (Cr) level <1.5 × ULN; international normalized ratio (INR) or prothrombin time (PT) or activated partial thromboplastin time (APTT) ≤1.5 × ULN.
- No known history of allergy to the study drugs.
- No prior radiotherapy to the planned radiation site.
- Non-pregnant and non-lactating women.
- For HIV-positive patients: at the initiation of the study, a stable combined antiretroviral therapy (CART) regimen must be used, with an HIV viral load of <50 copies/mL or below the limit of detection, and a CD4+ T-cell count >300/µL. Patients will be closely monitored during the study, and CART management will follow antiviral treatment guideline recommendations.
- Signed informed consent form.
Exclusion Criteria:
- Perianal squamous cell carcinoma originating from the perianal skin without invasion of the anal canal or anal sphincter. (For tumors with an ill-defined primary site, if clinical judgment indicates the main tumor mass involves the anal canal or is associated with anal sphincter invasion requiring sphincter-preserving chemoradiotherapy, the patient is eligible for inclusion.)
- Perianal Paget's disease.
- Pregnant or lactating women.
- Severe comorbidities or any medical/psychiatric condition deemed unsuitable for participation in this study.
- Patients with prior antitumor immunotherapy (e.g., anti-CTLA-4, anti-PD-1, or anti-PD-L1 monoclonal antibodies, etc.), with the exception of anti-HPV vaccination.
- History of other malignancies diagnosed within the past 3 years, except for curatively treated basal cell carcinoma of the skin and/or completely resected carcinoma in situ of the cervix, breast, or thyroid.
- Requires chronic use of immunosuppressive medications.
- Patients with severe autoimmune diseases, including but not limited to: symptomatic interstitial lung disease, or active infectious/non-infectious pneumonia; active inflammatory bowel disease (including Crohn's disease, ulcerative colitis); rheumatoid arthritis; scleroderma; systemic lupus erythematosus; autoimmune vasculitis; myasthenia gravis; myositis; autoimmune hepatitis; antiphospholipid syndrome; Wegener's granulomatosis; Sjögren's syndrome; Guillain-Barré syndrome; or multiple sclerosis, etc.
- History of organ transplantation or allogeneic stem cell transplantation.
- Patients with laboratory test values not meeting the relevant criteria within 7 days prior to enrollment.
- Patients with significantly impaired cardiac, hepatic, pulmonary, renal, or bone marrow function.
- Patients with severe, uncontrolled medical conditions or infections. Examples include: severe myocardial infarction, heart failure, unstable angina, or unstable arrhythmia within the past 6 months; respiratory failure and chronic obstructive pulmonary disease; active hepatitis B virus (HBV) infection (HBV-DNA ≥2000 U/mL); hepatitis C virus (HCV) infection; active tuberculosis infection, etc.
- Concurrent use of other investigational drugs or participation in other clinical trials.
- Patients who refuse or are unable to sign the informed consent form for participation in the trial.
- Patients with known allergies or contraindications to the investigational anti-tumor drug or any of its excipients.
- Patients deemed by the investigator to be unsuitable for participation in the study and unlikely to comply with the study procedures, restrictions, and requirements.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Количество рук
Оружие и интервенции
Группа участников / АрмияГруппа участников / Армия |
Вмешательство/лечениеВмешательство/лечение |
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Активный компаратор: Control Arm: Mitomycin + Capecitabine + IMRT
Standard definitive chemoradiotherapy for limited-stage anal squamous cell carcinoma: Intensity-modulated radiotherapy (IMRT) concurrent with capecitabine and mitomycin.
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Intensity-modulated radiotherapy (IMRT) will be administered:
Oral capecitabine at 825 mg/m² twice daily on days of radiotherapy, concurrent with IMRT, as part of the chemoradiotherapy backbone for both study arms.
Intravenous mitomycin at 10 mg/m² as a single bolus dose on day 1 of radiotherapy, administered only to the control arm as part of the standard chemoradiotherapy regimen.
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Экспериментальный: Experimental Arm: Sintilimab + Capecitabine + IMRT
Innovative immunotherapy replacement regimen: Intensity-modulated radiotherapy (IMRT) concurrent with capecitabine and sintilimab (PD-1 inhibitor) for limited-stage anal squamous cell carcinoma.
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Intensity-modulated radiotherapy (IMRT) will be administered:
Oral capecitabine at 825 mg/m² twice daily on days of radiotherapy, concurrent with IMRT, as part of the chemoradiotherapy backbone for both study arms.
Intravenous sintilimab at 200 mg every 3 weeks, administered concurrently with capecitabine and IMRT to the experimental arm as an immunotherapy replacement for mitomycin.
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Что измеряет исследование?
Первичные показатели результатов
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Clinical Complete Response (cCR) Rate
Временное ограничение: 6 months after radiotherapy
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cCR is defined as the simultaneous fulfillment of the following criteria: ① Digital rectal examination (DRE): no palpable nodule or ulcer, with only a smooth scar or fibrosis remaining; ② Anoscopy: no macroscopic evidence of residual tumor, with histopathological biopsy required for confirmation if suspicious lesions are present; ③ PET/CT: no residual tumor or new metastatic disease, or no evidence of residual tumor on contrast-enhanced CT or MRI if PET/CT is unavailable.
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6 months after radiotherapy
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Grade ≥3 acute TRAEs
Временное ограничение: From the start of local treatment to 90 days after the completion of treatment
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According to the CTCAE version 5.0 criteria, non-hematologic toxicities of grade ≥3 (including cutaneous and mucosal reactions, gastrointestinal reactions, and genitourinary reactions), hematologic toxicities (including leukopenia, neutropenia, thrombocytopenia, and anemia, excluding lymphopenia), and immune-related adverse events occurring from the start of local treatment to 90 days after the completion of treatment will be evaluated.
The investigator will determine whether these events are treatment-related adverse events.
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From the start of local treatment to 90 days after the completion of treatment
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Вторичные показатели результатов
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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AEs rate
Временное ограничение: 2 years after randomization
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The incidence and severity of all-grade adverse events during treatment and post-treatment will be evaluated according to CTCAE version 5.0, and investigators will determine whether they are immune-related adverse events (irAEs).
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2 years after randomization
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Quality of life (QoL) in cancer patients
Временное ограничение: Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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Quality of life in cancer patients will be evaluated using the European Organisation for Treatment and Research of Cancer (EORTC) Quality of Life Questionnaires QLQ-C30.
The scoring and interpretation of the QLQ-C30 scales were performed according to the EORTC guidelines.
Each item is scored from 0 to 100, with higher scores indicating better functioning on the functional scales/items and more severe symptoms on the symptom scales/items.
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Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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quality of life (QoL) in anal cancer patients
Временное ограничение: Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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Anal cancer-specific quality of life will be evaluated using the European Organisation for Treatment and Research of Cancer (EORTC) Quality of Life Questionnaires QLQ-ANL27.
The scoring and interpretation of the QLQ-ANL27 scales were performed according to the EORTC guidelines.
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Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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Anal function
Временное ограничение: Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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Anal function will be evaluated using the Wexner incontinence score.
This scoring system consists of 5 items evaluating the frequency of gas incontinence, frequency of liquid incontinence, frequency of solid incontinence, frequency of wearing pads, and lifestyle alterations, with a score ranging from 0-4 for each question.
The total score is calculated, with higher scores indicating poorer anal function.
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Baseline, 3 days after completion of radiotherapy, 1 month after radiotherapy, 3 months after radiotherapy, 6 months after radiotherapy, every 3 months up to 2 years after randomization
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PFS
Временное ограничение: 2 years after randomization
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Progression-free survival (PFS) is defined as the time from enrollment to the first documentation of disease recurrence or progression per RECIST 1.1 criteria, or death from any cause, whichever occurs first.
For participants without any event, PFS will be censored at the last follow-up.
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2 years after randomization
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CFS
Временное ограничение: 2 years after randomization
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Colostomy-free survival (CFS) is defined as the time from enrollment to the first occurrence of permanent colostomy (due to tumor residual/recurrence, severe treatment-related toxicity leading to loss of anal function, or disease progression/recurrence) or death from any cause, whichever occurs first.
For participants without any event, CFS will be censored at the last follow-up.
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2 years after randomization
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LRFS
Временное ограничение: 2 years after randomization
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Locoregional recurrence-free survival (LRFS) is defined as the time from enrollment to the first occurrence of locoregional disease progression (local recurrence or regional lymph node recurrence) or death from any cause, whichever occurs first. For participants without any event, LRFS will be censored at the last follow-up. Local recurrence (LR) is defined as the reappearance of tumor in the anal canal, perianal skin, rectum, or anastomotic site. Persistent disease (tumor that never achieved clinical complete response [cCR] after chemoradiotherapy) is considered an event for statistical analysis, but assessment of residual disease within 6 months after radiotherapy completion is not recommended. Regional lymph node recurrence is defined as the reappearance of tumor in regional lymph node drainage areas within the radiation field, including inguinal, mesorectal, presacral, internal iliac, external iliac, and obturator lymph nodes. |
2 years after randomization
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DMFS
Временное ограничение: 2 years after randomization
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Distant metastasis-free survival (DMFS) is defined as the time from enrollment to the first occurrence of distant metastasis or death from any cause, whichever occurs first.
For participants without any event, DMFS will be censored at the last follow-up.
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2 years after randomization
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OS
Временное ограничение: 2 years after randomization
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Overall survival (OS) is defined as the time from enrollment to death from any cause.
For participants without any event, OS will be censored at the last follow-up.
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2 years after randomization
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Rate of treatment interruption
Временное ограничение: 2 years after randomization
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The proportion of any unplanned radiotherapy interruptions during the scheduled radiotherapy course due to treatment-related adverse events.
|
2 years after randomization
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Соавторы и исследователи
Спонсор
Спонсор
Следователи
Следователи
- Главный следователь: Jing Jin, MD, PhD, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Начало исследования
Первичное завершение (Оцененный)
Первичное завершение
Завершение исследования (Оцененный)
Завершение исследования
Даты регистрации исследования
Первый отправленный
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Первый опубликованный
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее опубликованное обновление
Последнее отправленное обновление, отвечающее критериям контроля качества
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Новообразования по локализации
- Новообразования
- Кишечные заболевания
- Желудочно-кишечные новообразования
- Новообразования пищеварительной системы
- Заболевания пищеварительной системы
- Желудочно-кишечные заболевания
- Колоректальные новообразования
- Новообразования кишечника
- Заболевания прямой кишки
- Заболевания ануса
- Новообразования прямой кишки
- Новообразования ануса
- Органические химические вещества
- Гетероциклические соединения, 1-кольцо
- Гетероциклические соединения
- Гетероциклические соединения, 2-кольцо
- Гетероциклические соединения, слитое кольцо
- Терапия
- Нуклеиновые кислоты, нуклеотиды и нуклеозиды
- Индолы
- Дезоксицитидин
- Цитидин
- Пиримидиновые нуклеозиды
- Пиримидины
- Нуклеозиды
- Урацил
- Пиримидиноны
- Лучевая терапия
- Хиноны
- Азирины
- Дезоксирибонуклеозиды
- Флуорурацил
- Лучевая терапия, конформная
- Лучевая терапия, компьютерная помощь
- Митомицины
- Индокекиноны
- Капецитабин
- Митомицин
- Лучевая терапия, модулированная интенсивностью
- Синтилимаб
Другие идентификационные номера исследования
Другие идентификационные номера исследования
- NCC6140
Планирование данных отдельных участников (IPD)
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Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
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