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Hypofractionated Radiotherapy Plus GM-CSF, Pomalidomide and Glofitamab for Newly Diagnosed PCNS-DLBCL

2 de agosto de 2026 atualizado por: Zhijuan Lin, The First Affiliated Hospital of Xiamen University

A Prospective Phase II Clinical Study to Evaluate the Efficacy and Safety of Hypofractionated Radiotherapy Combined With Granulocyte-Macrophage Colony-Stimulating Factor, Pomalidomide and Glofitamab in Patients With Newly Diagnosed Primary Central Nervous System Diffuse Large B-Cell Lymphoma

This prospective study was conducted to evaluate the efficacy and safety of hypofractionated radiotherapy combined with granulocyte-macrophage colony-stimulating factor, pomalidomide and glofitamab in patients with newly diagnosed primary central nervous system diffuse large B-cell lymphoma.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

53

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Zhijian Lin, Dr
  • Número de telefone: +86 15960283462
  • E-mail: zjuan_lin@126.com

Locais de estudo

    • Fujian
      • Xiamen, Fujian, China, 361003
        • Recrutamento
        • The First Affiliated Hospital of Xiamen University
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  1. Written informed consent must be obtained before any study-related procedures.
  2. Age ≥18 years, regardless of sex, with an expected survival time >3 months.
  3. Histologically confirmed diffuse large B-cell lymphoma (DLBCL).
  4. Newly diagnosed patients with primary central nervous system diffuse large B-cell lymphoma (PCNSL).
  5. No previous treatment with bispecific antibodies.
  6. B-cell non-Hodgkin lymphoma with at least one measurable lesion according to RECIST 1.1 criteria, or detectable abnormal monoclonal B cells by cerebrospinal fluid (CSF) flow cytometry.
  7. Adequate organ function meeting the following laboratory criteria:

    • Total bilirubin ≤1.5 × upper limit of normal (ULN);
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN;
    • Serum creatinine ≤1.5 × ULN and creatinine clearance ≥60 mL/min (calculated using the Cockcroft-Gault formula);
    • Adequate coagulation function, defined as international normalized ratio (INR) or prothrombin time (PT) ≤1.5 × ULN.
  8. Women of childbearing potential must have a negative urine or serum pregnancy test within 3 days before the first dose of study treatment (Cycle 1 Day 1). If urine pregnancy testing cannot confirm a negative result, a serum pregnancy test is required. Women of non-childbearing potential are defined as those who are postmenopausal for ≥1 year or have undergone surgical sterilization or hysterectomy.
  9. All participants with reproductive potential (male or female) must use highly effective contraception with a failure rate <1% per year during treatment and for 120 days after the last dose of study drug (or 180 days after the last dose of chemotherapy).

Exclusion Criteria:

  1. Loss of CD20 expression in B-cell non-Hodgkin lymphoma.
  2. Active acute or chronic hepatitis B or hepatitis C infection, including:

    • HBV DNA >2,000 IU/mL or >10⁴ copies/mL without willingness to receive regular antiviral therapy;
    • HCV RNA >10³ copies/mL;
    • Concurrent positivity for HBsAg and anti-HCV antibody.
  3. Receipt of anti-hematologic malignancy therapy within 2 weeks or within 5 pharmacokinetic half-lives before treatment initiation, whichever is longer.
  4. Inadequate bone marrow reserve, defined as platelet count <30 ×10⁹/L or absolute neutrophil count <1.0 ×10⁹/L.
  5. Clinically significant pulmonary diseases, including:

    • Chronic obstructive pulmonary disease (COPD) with FEV1 <50% of predicted value;
    • Moderate or severe persistent asthma within the past 2 years or uncontrolled asthma of any severity.
  6. Uncontrolled hypertension despite optimal medical management (systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg), history of hypertensive crisis, or hypertensive encephalopathy.
  7. Symptomatic congestive heart failure (NYHA class II-IV), symptomatic or poorly controlled arrhythmias, congenital long QT syndrome, or corrected QT interval (QTc) >500 ms (Fridericia correction).
  8. Receipt of hypofractionated radiotherapy within 4 weeks before the first treatment. Patients receiving radiotherapy >4 weeks before enrollment must have no ongoing radiation-related toxicities, no requirement for corticosteroids, and no evidence of radiation pneumonitis, hepatitis, enteritis, or other radiation-related complications.
  9. Difficulty swallowing oral medications.
  10. History or presence of pulmonary fibrosis, interstitial lung disease, pneumoconiosis, drug-induced pneumonitis, or severe pulmonary dysfunction.
  11. HIV infection (positive HIV-1/2 antibody) or known syphilis infection.
  12. Presence of unhealed wounds, fractures, gastric or duodenal ulcers, persistent positive fecal occult blood test, ulcerative colitis, or other conditions associated with risk of gastrointestinal bleeding or perforation as determined by the investigator.
  13. Active or uncontrolled severe infection, including severe infection requiring hospitalization due to infection, bacteremia, or severe pneumonia within 4 weeks before the first dose.
  14. Major surgery or significant traumatic injury within 4 weeks before the first dose.
  15. Use of traditional Chinese medicine with antitumor indications within 2 weeks before the first dose.
  16. Known hypersensitivity to any component of bispecific antibodies or GM-CSF preparations.
  17. Receipt of treatment in another clinical trial within 4 weeks before the first dose.
  18. Pregnant or breastfeeding women.
  19. Active autoimmune disease or history of autoimmune disease, including but not limited to autoimmune hepatitis, interstitial pneumonia, enteritis, vasculitis, and nephritis. Patients requiring medical intervention with bronchodilators for asthma are excluded. The following conditions are permitted: vitiligo, psoriasis, alopecia, or controlled type I diabetes not requiring systemic treatment, and hypothyroidism controlled with hormone replacement therapy.
  20. Any other acute or chronic disease, psychiatric condition, or abnormal laboratory finding that may:

    • Increase the risk associated with study participation or administration of study treatment;
    • Interfere with interpretation of study results;
    • Render the patient unsuitable for participation according to the investigator's judgment.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: hypofractionated radiotherapy combined with granulocyte-macrophage colony-stimulating

After signing the informed consent, patients may receive pretreatment with dexamethasone (10 mg/day, maximum dose 30 mg) and/or pomalidomide 4 mg/day for up to 7 days. In Cycle 1, patients receive hypofractionated radiotherapy at 5 Gy per day for 3 consecutive days. One to two cycles of radiotherapy will be administered for a single target lesion, with the radiotherapy regimen determined by the investigator.

GM-CSF at 400 μg once daily is administered for 3 consecutive days starting on Day 1 after radiotherapy completion. Pomalidomide 4 mg once daily is given for 14 consecutive days starting on Day 1 after radiotherapy completion. If pomalidomide is used during pretreatment, the total duration of pomalidomide (pretreatment plus post-radiotherapy administration) shall not exceed 14 days. Dose escalation of glofitamab commences on Day 7 after radiotherapy completion.

Cycles 2 to 6 are administered on a 21-day cycle schedule. GM-CSF 400 μg once daily is given for 3 consecutive days start

Treatment Regimen (Brief Version)

  • Hypofractionated radiotherapy: 5 Gy/day for 3 days, continued until disease progression, unacceptable toxicity, withdrawal of consent, initiation of new anti-cancer therapy, or other protocol-defined termination.
  • GM-CSF: 400 μg subcutaneously once daily for 3 days after radiotherapy and the first 3 days of each subsequent cycle.
  • Pomalidomide: 25 mg orally once daily for 14 days after radiotherapy, followed by days 1-14 of each 21-day cycle (cycles 2-6), with dose adjustment based on renal function and blood counts.
  • Glofitamab (bispecific antibody): Rituximab on day 1, glofitamab step-up dosing on day 8, followed by 30 mg every 21 days for 6 cycles.
  • Treatment duration: Until disease progression, unacceptable toxicity, withdrawal of consent, initiation of new anti-cancer therapy, or other protocol-defined discontinuation.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
CR (Complete Response Rate)
Prazo: Up to 12 months
The primary efficacy endpoint is the complete response (CR) rate, defined as the proportion of patients achieving complete response according to the Lugano response criteria.
Up to 12 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
ORR (Objective Response Rate)
Prazo: Up to 12 months
Secondary efficacy endpoints include objective response rate (ORR), duration of response (DoR), and safety profile. ORR is defined as the proportion of patients achieving complete response or partial response according to the Lugano response criteria.
Up to 12 months
Duration of Response (DoR)
Prazo: Up to 12 months
Duration of response is defined as the time from the first documented response (complete response or partial response) to disease progression, death, or the last disease assessment.
Up to 12 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

25 de julho de 2026

Conclusão Primária (Estimado)

31 de dezembro de 2029

Conclusão do estudo (Estimado)

31 de dezembro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

22 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

2 de agosto de 2026

Primeira postagem (Real)

6 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

2 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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