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Идёт набор NCT05833893

Clinical Study of XPO1 Inhibitor Selinexor Combined With COPL in Newly Diagnosed Advanced NK/T-cell Lymphoma

Фаза II С лечением nk/T-cell Lymphoma Newly Diagnosed Advanced Lymphoma

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: XPO1 inhibitor.
Кому может быть актуально
Состояния в реестре: nk/T-cell Lymphoma, Newly Diagnosed, Advanced Lymphoma. Базовые параметры: от 14 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

Patients with newly diagnosed, pathologically confirmed NK/T-cell lymphoma of stage III-IV treated with XCOPL regimen. 3 weeks for a cycle, with a total of 6-8 cycles.

Подробное описание

Patients with newly diagnosed, pathologically confirmed NK/T-cell lymphoma of stage III-IV treated with XCOPL regimen. 3 weeks for a cycle, with a total of 6-8 cycles. Initial safety and PET-CT assessment were performed after 3 cycles of treatment (which could be delayed until 4 cycles of treatment in special cases). Patients who achieved partial remission or above will continue the original regimen, and patients who did not achieve partial remission or above will perform re-biopsy and be excluded from the group. Patients who remain partial remission by PET-CT evaluation after 6 cycles may switch to a second-line regimen (referring to NCCN guidelines, GDP regimen combined with selinexor is recommended). Chemotherapy will be performed for up to 8 cycles (followed by autologous or allogeneic hematopoietic stem cell transplantation), after which follow-up period was entered. It is recommended to perform ultrasound or CT evaluation, peripheral blood ctDNA and EBV copy number every three months during the first year of follow-up, and PET-CT evaluation every half a year.

Вмешательства

  • Препарат XPO1 inhibitor
    COPL + XPO1 inhibitor (Selinexor, 60 mg, po., d1,8,15)

Первичные конечные точки

  • response rate [Срок оценки: 1-year]
  • Incidence of Treatment-Emergent Adverse Events [Срок оценки: 1-year]
Вторичные конечные точки (3)
  • the 1-year PFS [Срок оценки: 1-year]
  • the 1-year OS [Срок оценки: 1-year]
  • the ctDNA and EBV copy number in peripheral blood [Срок оценки: 1-year]

Критерии участия

Критерии включения

  • Age≥14 years, male or female;
  • Pathologically confirmed newly diagnosed NK/T cell lymphoma according to WHO classification criteria 2016;
  • At least one measurable lesion, defined as bidimensionally measurable, intranodal lesion > 1.5 cm in short axis and extranodal lesion > 1.0 cm in short axis;
  • ECOG score 0\~2;
  • Clinical stage III\~IV;
  • Normal major organ function, meeting the following definitions: Hematology: WBC ≥ 3.5 x 10 9/L, PLT ≥ 75 x 10 9/L, Hb ≥ 80 g/L; Liver and kidney function: AST and ALT ≤ 3.0 ULN; TBIL ≤ 2.0 mg/dL; CCr ≥ 60 mL/min; liver and kidney function impairment caused by tumor compression is not limited by this; Fibrinogen: normal at first cycle
  • Expected survival > 6 months
  • Agree to use effective contraception;
  • Understand and voluntarily sign written informed consent

Критерии исключения

  • Prior allogeneic HCT (allo-HCT)
  • Active autoimmune disease
  • Primary central nervous system lymphoma;
  • Patients with infection which requiring treatment. Could be re-enrollment after infection control;
  • Known history of human immunodeficiency virus (HIV) infection
  • Known hypersensitivity to the study drug or any of its excipients;
  • Presence of other active malignancy requiring treatment that could interfere with this study;
  • Patients with other conditions not suitable for enrollment as judged by the investigator.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Китай · 1 центр
  • ChinaPLAGH — Пекин

Публикации

  • Benkova K, Mihalyova J, Hajek R, Jelinek T. Selinexor, selective inhibitor of nuclear export: Unselective bullet for blood cancers. Blood Rev. 2021 Mar;46:100758. doi: 10.1016/j.blre.2020.100758. Epub 2020 Sep 15. PMID 32972802
  • Tse E, Kwong YL. Diagnosis and management of extranodal NK/T cell lymphoma nasal type. Expert Rev Hematol. 2016 Sep;9(9):861-71. doi: 10.1080/17474086.2016.1206465. Epub 2016 Jul 8. PMID 27347812
  • Lim SH, Hong JY, Lim ST, Hong H, Arnoud J, Zhao W, Yoon DH, Tang T, Cho J, Park S, Ko YH, Kim SJ, Suh C, Lin T, Kim WS. Beyond first-line non-anthracycline-based chemotherapy for extranodal NK/T-cell lymphoma: clinical outcome and current perspectives on salvage therapy for patients after first relapse and progression of disease. Ann Oncol. 2017 Sep 1;28(9):2199-2205. doi: 10.1093/annonc/mdx316. PMID 28911074

Идентификаторы

NCT: NCT05833893 · XCOPL - NK/T -P01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗