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Phase II Study With Ga101-DHAP as Induction Therapy in Relapsed/Refractory DLBCL Patients (GIOTTO)

1 июня 2022 г. обновлено: Fondazione Italiana Linfomi ONLUS

Phase II Study With Ga101-DHAP as Induction Therapy in Relapsed/Refractory Diffuse Large B-cell Lymphoma (DLBCL) Patients Before High-Dose Chemotherapy BEAM With Autologous Stem Cell Transplantation (ASCT)

Aim of this trial is to assess the efficacy of new anti-CD20 antibody (GA101) in association with DHAP as induction therapy before high dose chemotherapy BEAM with ASCT in patients with relapsed/refractory DLBCL.

Обзор исследования

Статус

Прекращено

Вмешательство/лечение

Подробное описание

This is a prospective, multicenter, single arm, phase II trial in young patients (18-65 years) affected by relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) at diagnosis,eligible to high-dose therapy.

Aim of the study is to assess whether the addition of GA101 to DHAP is more promising than standard R-DHAP, as induction therapy before high dose chemotherapy BEAM with ASCT with respect to response.

The study is designed primarily to evaluate the efficacy of GA101-DHAP in patients with DLBCL who have relapsed or are refractory to one chemotherapy regimen and secondarily to assess safety and capability to mobilize peripheral stem cells The study is designed with two stages and with stopping rules after the first stage. In particular, at the end of the first stage, the study will be stopped if the efficacy is too low or if the toxicity, measured during the drug administration period, is too high with respect to pre-defined thresholds. .

Тип исследования

Интервенционный

Регистрация (Действительный)

29

Фаза

  • Фаза 2

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Места учебы

      • Bolzano, Италия, 39100
        • Ospedale di Bolzano, Reparto di Ematologia & CTMO
      • Firenze, Италия, 50139
        • A.O. Universitaria Careggi
      • Mestre, Италия, 30174
        • Ospedale dell'Angelo, U.O. Ematologia
      • Modena, Италия, 41124
        • A.O. Universitaria Policlinico Di Modena
      • Pavia, Италия, 27100
        • Ematologia Policlinico San Matteo
      • Perugia, Италия, 06132
        • AO di Perugia S. Maria della misericordia
      • Roma, Италия
        • Ematologia e Trapianto Istituto Regina Elena IFO
      • Roma, Италия, 00149
        • Ematologia Ospedale S.Camillo Forlanini
      • Roma, Италия, 00161
        • Policlinico Umberto I - Università "La Sapienza"
    • VI
      • Vicenza, VI, Италия, 36100
        • Ospedale San Bortolo

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

От 18 лет до 65 лет (Взрослый, Пожилой взрослый)

Принимает здоровых добровольцев

Да

Полы, имеющие право на обучение

Все

Описание

Inclusion Criteria:

  1. 18≥ Age < 65
  2. Relapsed/refractory disease after receiving one line of standard R-CHOP like chemotherapy
  3. Diffuse Large B-cell Lymphoma at relapse. The re-biopsy is particularly recommended if relapse is over 1 year from previous complete remission. If this is harmful for the patient, the patient can be enrolled if archival tumor sample and block from first diagnosis are available.
  4. Measurable and/or evaluable disease
  5. Any Ann Arbor stage and IPI group at relapse
  6. Performance status < 2 according to Eastern Cooperative Oncology Group (ECOG) scale unless due to lymphoma
  7. No Central Nervous System (CNS) disease (meningeal and/or brain involvement by lymphoma)
  8. Adequate haematological counts: Absolute Neutrophil Count (ANC) > 1.5 x 109/L, Hgb > 10.5 g/dl (transfusion independent), Platelet count > 75 x 109/L (transfusion independent), with the exception of cytopenia due to lymphoma bone marrow involvement
  9. Normal liver function (ALP, AST, ALT, GGT, conjugated bilirubin total < 2 x ULN) if not related to lymphoma
  10. Normal kidney function (creatinine clearance >= 80 ml/min)
  11. Cardiac ejection fraction > 50% (MUGA scan or echocardiography)
  12. Normal lung function
  13. Absence of active infections
  14. Non peripheral neuropathy or active neurological non neoplastic disease of CNS
  15. Non major surgical intervention prior 3 months to randomization if not due to lymphoma and/or not other disease life-threatening that can compromise chemotherapy treatment
  16. Disease free of prior malignancies other than lymphoma for > 3 years with exception of currently treated squamous cell and basal cell carcinoma of the skin or carcinoma in situ of the cervix or breast
  17. Life expectancy > 6 months
  18. No psychiatric illness that precludes understanding concepts of the trial or signing ten informed consent
  19. Written informed consent
  20. Women must be:

    1. postmenopausal for at least 1 year (must not have had a natural menses for at least 12 months)
    2. surgically sterile (have had a hysterectomy or bilateral oophorectomy, tubal ligation, or otherwise be incapable of pregnancy),
    3. abstinent (at the discretion of the investigator/per local regulations), or
    4. if sexually active, be practicing a highly effective method of birth control (eg, prescription oral contraceptives, contraceptive injections, contraceptive patch, intrauterine device, double-barrier method (eg, condoms, diaphragm, or cervical cap, with spermicidal foam, cream, or gel, male partner sterilization) as local regulations permit, before entry, and must agree to continue to use the same method of contraception throughout the study. They must also be prepared to continue birth control measures for at least 18 months after terminating treatment.
  21. Women of childbearing potential must have a negative serum or urine beta-human chorionic gonadotropin (beta-hCG) pregnancy test at screening
  22. Men must agree to use an acceptable method of contraception (for themselves or female partners as listed above) for the duration of the study. Men must agree to use a double barrier method of birth control and to not donate sperm during the study and for 3 months after receiving the last dose of study drug.

Exclusion Criteria:

  1. Diagnosis of Lymphoblastic Lymphoma, Burkitt Lymphoma, Non Hodgkin Lymphoma CD20 negative, Mantle Cell Lymphoma, Follicular Lymphoma, Primary Mediastinal Lymphoma
  2. Age ≥ 65 years
  3. Patients ineligible to high-dose chemotherapy
  4. Performance status > 2 according to ECOG scale if not due to lymphoma
  5. Patients who previously received GA101 (obinutuzumab) are excluded.
  6. Patient has known or suspected hypersensitivity or intolerance to Rituximab
  7. Patient has received an experimental drug or used an experimental medical device within 4 weeks before the planned start of treatment. Concurrent participation in nontreatment studies is allowed, if it will not interfere with participation in this study.
  8. CNS disease (meningeal and/or brain involvement by lymphoma)
  9. History of clinically relevant liver or renal insufficiency; significant cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, rheumatologic, hematologic, psychiatric, or metabolic disturbances
  10. Positive test results for chronic hepatitis B infection (defined as positive HBsAg serology). Patients with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if HBV DNA is undetectable. These patients must be willing to undergo monthly DNA testing.
  11. Positive test results for hepatitis C (HCV antibody serology testing). Patients positive for HCV antibody are eligible only if PCR is negative for HCV RNA.
  12. Known history of HIV seropositive status. For patients with unknown HIV status, HIV testing will be performed at screening if required by local regulations.
  13. Uncontrolled diabetes (if receiving antidiabetic agents, subjects must be on a stable dose for at least 3 months before first dose of study drug
  14. Uncontrolled or severe cardiovascular disease including myocardial infarction within six months of enrollment, New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, clinically significant pericardial disease, or cardiac amyloidosis
  15. Cardiac ejection fraction < 45% (MUGA scan or echocardiography)
  16. Creatinine clearance < 45 ml/min
  17. Presence of major neurological disorders
  18. Active infection
  19. Major surgical intervention prior 3 months to randomization if not due to lymphoma and/or other disease life-threatening that can compromise chemotherapy treatment
  20. Prior malignancies other than lymphoma in the last 3 years with exception of currently treated squamous cell and basal cell carcinoma of the skin or carcinoma in situ of the cervix or breast
  21. Life expectancy < 6 months
  22. Any other coexisting medical or psychological condition that would preclude participation in the study or compromise ability to give informed consent.
  23. If female, the patient is pregnant or breast-feeding.

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

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: GA101_DHAP

Patients receive: GA101-DHAP x 2, restaging, mobilization and collection of peripheral blood stem cells, + GA101-DHAP x 2, restaging with PET and CT and consolidation with BEAM and ASCT in patients in response (CR+PR).

During the treatment period of four cycles, all patients will receive a total of four 28-day courses of chemotherapy.

Aim of the study is to assess whether the addition of GA101 to DHAP is more promising than standard R-DHAP, as induction therapy before high dose chemotherapy BEAM with ASCT with respect to response.

Scheme of treatment:

  • GA101 1000 mg iv day 1, 8, 15 on first cycle (starting from cycle 2, GA101 1000 mg day 1)
  • Cisplatin 100 mg/sqm iv day 1 of every cycles in 24-hours infusion
  • Cytarabine 2000 mg/sqm in 3-hours infusion every 12 hours iv day 2 of every cycles
  • Dexamethasone 40 mg day 1-4 of every cycles
  • Pegfilgrastim 6 mg sc single dose 24 hours after the end of chemotherapy or G-CSF from day 4 till stem cell harvest during mobilization's course (II o III cycle GA101-DHAP)
  • GA101 1000 mg iv 24 hours before apheresis as purging in vivo during second courses of therapy

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Aim of this trial is to assess the efficacy of new anti-CD20 antibody (GA101) in association with DHAP as induction therapy before high dose chemotherapy BEAM with ASCT in patients with relapsed/refractory DLBCL.
Временное ограничение: 4 months

Primary objective is to assess whether the treatment achieves an absolute increase of the CR proportion of at least 20% (from 30% to 50%) with respect to the standard treatment.

The complete response rate (CR) evaluated by PET scan after four cycles of GA101-DHAP before ASCT according to Cheson criteria.

4 months

Вторичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Overall Response Rate (ORR) prior to consolidation with BEAM and ASCT
Временное ограничение: 2 years
A patient is defined as a responder if she/he has a complete or partial response, evaluated by PET/TC, after four cycles of GA101-DHAP
2 years
Progression free survival (PFS) at 6 month after the end of treatment (EOT)
Временное ограничение: 6 month
Measured from the date of starting salvage therapy to the date of disease progression, relapse or death from any cause. Responding patients and patients who are lost to follow up will be surveyed at their last assessment date.
6 month
Overall Survival (OS) at 2 years after the EOT
Временное ограничение: 2 years
Measured from the date of starting salvage therapy to the date of death from any cause. Patients alive at the time of the final analysis will be surveyed at the date of the last contact. For both PFS and OS minimum follow up time required for all patients will be 2 years.
2 years
Toxicity: Severe, life-threatening, fatal (grade 3, 4 and 5) and/or serious adverse events
Временное ограничение: 2 years
Severe, life-threatening, fatal (grade 3, 4 and 5) and/or serious adverse events are defined according to "Common Terminology Criteria for Adverse Events" (CTCAE), version 4.0. and adverse events of special interests (AESI)
2 years
The hematopoietic cell mobilization
Временное ограничение: 2 years
Mobilizing potential: amount of CD34 + stem cell collected /Kg
2 years
Feasibility: the rate of patients actually proceeding to ASCT
Временное ограничение: 2 years
Proportion of patients successfully completing ASCT
2 years

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Следователи

  • Главный следователь: Maurizio Martelli, MD, Dipartimento di Biotecnologie Cellulari ed Ematologia, "La Sapienza" Roma

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Действительный)

5 ноября 2014 г.

Первичное завершение (Действительный)

1 февраля 2018 г.

Завершение исследования (Действительный)

23 июня 2020 г.

Даты регистрации исследования

Первый отправленный

17 февраля 2015 г.

Впервые представлено, что соответствует критериям контроля качества

26 февраля 2015 г.

Первый опубликованный (Оценивать)

27 февраля 2015 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

6 июня 2022 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

1 июня 2022 г.

Последняя проверка

1 июня 2022 г.

Дополнительная информация

Термины, связанные с этим исследованием

Планирование данных отдельных участников (IPD)

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НЕТ

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. .

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