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

2026年8月2日 更新者: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.

調査の概要

研究の種類

介入

入学 (推定)

53

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Zhijian Lin, Dr
  • 電話番号:+86 15960283462
  • メール:zjuan_lin@126.com

研究場所

    • Fujian
      • Xiamen、Fujian、中国、361003
        • 募集
        • The First Affiliated Hospital of Xiamen University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
CR (Complete Response Rate)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
ORR (Objective Response Rate)
時間枠: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)
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月25日

一次修了 (推定)

2029年12月31日

研究の完了 (推定)

2029年12月31日

試験登録日

最初に提出

2026年7月22日

QC基準を満たした最初の提出物

2026年8月2日

最初の投稿 (実際)

2026年8月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月6日

QC基準を満たした最後の更新が送信されました

2026年8月2日

最終確認日

2026年8月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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