このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

High Dose Rituximab for Initial Treatment of Indolent B-Cell Lymphomas

2017年5月9日 更新者:Jeremy Abramson, MD、Massachusetts General Hospital

Phase II Trial of Increased Dose Rituximab Plus Maintenance Rituximab for Initial Systemic Treatment of Indolent B-Cell Lymphomas

The purpose of this clinical trial is to see if increased doses of rituximab are safe and effective for the initial treatment of indolent B-cell lymphomas. Rituximab (Rituxan) is a type of drug called an "antibody" that specifically targets B-cell lymphoma cells, and is approved by the FDA for the treatment of indolent B-cell non-hodgkin lymphomas and certain other types of non-hodgkin lymphomas. Standard doses currently used may not be achieving maximal efficacy. Higher doses have been shown to be safe in other clinical trials, and may offer superior efficacy to the current standard dose. This trial also employs intermittent maintenance doses of rituximab at the standard dose, which has been shown to prolong remissions and survival in patients with relapsed indolent B-cell lymphomas. This trial is designed to show that higher dose rituximab plus maintenance rituximab can achieve similarly good results to chemotherapy approaches, but without chemotherapy-related toxicity.

調査の概要

詳細な説明

  • All participants will receive increased-dose rituximab through a vein in the arm once a week for 4 weeks (on Days 1, 8, 15, and 22 of the initial 28-day study cycle). This first cycle of study treatment is called the Induction Phase. If the participant responds well to the Induction Phase, they then may continue to the Maintenance Therapy Phase, where they will receive a lower dose of rituximab once every three months for up to 2 years.
  • During the Induction Phase, the following procedures will take place before the participant receives each dose of rituximab: medical review, physical exam, performance status, and ECG. Blood tests will be drawn about 30-60 minutes after the first dose of rituximab on Day 1. Samples will be drawn immediately before each dose and again 30-60 minutes after each dose on Days 1, 8, 15 and 22.
  • During the Maintenance Therapy Phase, the following procedures will take place before the participant receives each dose of rituximab: medical review, physical exam, performance status, ECG, blood tests and response assessments by CT scan.

研究の種類

介入

入学 (実際)

40

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。

研究場所

    • Massachusetts
      • Boston、Massachusetts、アメリカ、02115
        • Dana-Farber Cancer Institute
      • Boston、Massachusetts、アメリカ、02114
        • Massachusetts General Hospital

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

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Indolent B-Cell NHL of the following histologies:

    1. Follicular lymphoma (grades 1-3A);
    2. marginal zone lymphoma (extranodal, nodal or splenic):

      • Extranodal marginal zone lymphomas (MALT lymphomas) may not be candidates for cure with antibiotics or local radiotherapy. Patients who have failed antibiotics or local therapy are eligible for the protocol as long as they have measurable disease and are naive to chemotherapy and monoclonal antibody;
      • splenic marginal zone lymphoma patients may have received prior splenectomy as long as they have measureable disease and are naive to chemotherapy and monoclonal antibody therapy;
    3. Small lymphocytic lymphoma (must have less than 5000 circulating clonal B-lymphocytes);
    4. Indolent CD20+ B-cell lymphoma not otherwise specified with CD20+ expression
  • Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as 20mm or greater with conventional techniques or as 10mm or greater with spiral CT scan
  • No previous chemotherapy, antibody therapy or radioimmunotherapy for NHL. Patients previously treated with external bean radiation alone, surgery, or with antibiotics are eligible
  • 18 years of age or older
  • Life expectancy of greater than 3 months
  • ECOG performance status of 2 or less
  • Adequate bone marrow function
  • Use of adequate contraception

Exclusion Criteria:

  • Prior chemotherapy, monoclonal antibody therapy or radioimmunotherapy for lymphoma
  • Receiving any other investigational agent
  • Known brain metastases
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to rituximab
  • HIV positivity
  • Active hepatitis B infection
  • Candidate for curative radiotherapy, unless radiation therapy is considered too toxic (as in abdominal disease), or is refused by the patient
  • NYHA Classification III or IV disease
  • Uncontrolled intercurrent illness including, but not limited to ongoing or active infection that is not optimally treated with antibiotics, unstable angina pectoris, or psychiatric illness/social situations that would limit compliance with study requirements
  • Pregnant women
  • Individuals with a history of a different malignancy except for the following circumstances:

    1. disease-free for at least 1 year and are deemed by the investigator to be at low risk for recurrence of that malignancy;
    2. localized prostate cancer, prostate cancer with elevated PSA but no measurable disease on CT scans or bone scan, cervical cancer in situ; and
    3. non-melanoma skin cancers

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
他の:rituximab
single-arm, open-label, interventional
Increased dose (750 mg/m2) intravenously for 4 weekly doses followed by maintenance dosing once every three months for up to 2 years. Maintenance dose is standard (375 mg/m2).
他の名前:
  • リツキサン

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
Determine Complete Response Rate (CRR) of Increased Dose Rituximab in Indolent B-cell Lymphomas
時間枠:after a median number of 8 maintenance cycles, up to 24 weeks

CR requires all of the following:

  1. Regression to normal size on CT (≤ 1.5 cm in their greatest transverse diameter for nodes ≥ 1.5 cm before therapy). Previously involved nodes that were 1.1 to 1.5 cm in their greatest transverse diameter before treatment must have decreased to <1 cm in their greatest transverse diameter after treatment, or by more than 75% in the sum of the products of the greatest diameters (SPD).
  2. The spleen, if considered to be enlarged before therapy on the basis of a CT scan, must have regressed in size and must not be palpable on physical examination.
  3. If bone marrow is known to be involved at the beginning, then repeat biopsy documents clearance
after a median number of 8 maintenance cycles, up to 24 weeks

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall Response Rate (ORR)
時間枠:after a median number of 8 maintenance cycles, up to 24 weeks

Complete Response (CR): see definition in primary outcome

Partial Response (PR):

  1. ≥50% decrease in SPD of up to 6 largest dominant masses
  2. No new sites of disease or increase in the size of the other nodes, liver, or spleen.
  3. Splenic and hepatic nodules must regress by at least 50% in the SPD.

Overall Response (OR) = CR + PR.

after a median number of 8 maintenance cycles, up to 24 weeks
Progression-free Survival (PFS)
時間枠:5 years

Progressive Disease (PD) or Relapsed Disease (RD):

  1. Appearance of a new lesion(s) > 1.5 cm in any axis, ≥ 50% increase in SPD of more than one node, or ≥50% increase in longest diameter of a previously identified node > 1 cm in short axis.
  2. >50% increase from nadir in the SPD of any previous lesions PFS is number of participants who have not died or had PD or RD.
5 years
Incidence of Severity of Infusion Reactions, Infections and Neutropenia
時間枠:24 months
Toxicity grades: 1 = mild, 2 = moderate, 3 = severe, 4 = life-threatening
24 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 (実際)

2009年7月1日

一次修了 (実際)

2010年10月1日

研究の完了 (実際)

2015年8月1日

試験登録日

最初に提出

2009年5月6日

QC基準を満たした最初の提出物

2009年5月7日

最初の投稿 (見積もり)

2009年5月8日

学習記録の更新

投稿された最後の更新 (実際)

2017年6月9日

QC基準を満たした最後の更新が送信されました

2017年5月9日

最終確認日

2017年5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。

購読する