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Adjustment of Chemotherapy Duration in Follicular Lymphoma According to Minimal Residual Disease Status (FLMRD)

2021年6月20日 更新者:Meir Medical Center

Adjustment of Chemotherapy Duration in Follicular Lymphoma Patients According to Peripheral Blood or Bone Marrow Minimal Residual Disease Status

Follicular lymphoma (FL) is a chronic indolent malignancy, where treatment with 6 cycles of bendamustine obinutuzumab (BO) is highly effective but at a cost of increased adverse events.

Tumor specific DNA can be traced in blood and bone marrow of follicular lymphoma patients even after therapy, and when detected after lymphoma treatment it is referred to as minimal residual disease (MRD).

MRD elimination after effective lymphoma treatment is a marker for deep response and correlates with prolonged remission.

In this study we aim to omit chemotherapy after 4 cycles of treatment in patients achieving MRD elimination after 3 months of therapy, as well as complete metabolic response on positron emission computed tomography (PET-CT), hoping to preserve treatment effectiveness while reducing adverse events.

調査の概要

詳細な説明

Follicular lymphoma (FL) is the second most common type of non-Hodgkin's lymphoma, with an estimated incidence of 3.18 cases per 100000 people a year in the United States The disease is characterized by an indolent behavior, where often treatment is unnecessary at diagnosis, and a "watch & wait" approach is the standard of care for asymptomatic patients. FL is also a highly responsive disease for immuno-chemotherapeutic combinations, although most patients will eventually relapse. Since the disease is incurable & indolent in nature, the therapeutic strategy should aim for disease control, while using treatments with high safety profile in order to minimize the chance for life threatening adverse events.

Therapy with rituximab cyclophosphamide, doxorubicin, vincristine & prednisone (R-CHOP) combination & subsequent rituximab maintenance therapy for 24 months shows excellent results with a median progression free survival (PFS) of above a decade.

The more recent GALLIUM trial has shown that combining the monoclonal antibody obinutuzumab with chemotherapy is even more efficacious compared to rituximab combinations. When different combinations were examined in this trial the best results were achieved with the bendamustine-obinutuzumab (BO) combination with 3 year PFS of 84%. Unfortunately the trial also revealed a downside for this effective combination with higher rate of fatal adverse events among patients receiving 6 cycles of bendamustine combinations.

In patients with acute leukemia evaluation for minimal residual disease (MRD) is a routine procedure, and the nature & length of treatment are guided by MRD status at different time points during therapy.

Among FL patients treated with obinutuzumab-chemotherapy combinations, it has been shown that after 3 cycles of treatment about 90% of patients were MRD negative. In addition MRD negativity at the end of induction in either peripheral blood or bone marrow was found to be associated with improved outcomes in patients with 1st line treatment for FL as well as in the relapsed setting.

These findings raise the possibility for an MRD based treatment approach, where the duration of chemotherapy could be guided by MRD status at mid-induction. Eliminating chemotherapy while continuing immunotherapy after achievement of MRD negativity & complete metabolic remission on PET-CT at mid-induction could reduce treatment toxicity, while potentially preserving efficacy.

研究の種類

介入

入学 (予想される)

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。

研究連絡先

研究場所

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:

  1. Age 18 and above.
  2. FL grade I-IIIa, according to world health organization (WHO) classification, in patients who were not previously treated with chemotherapy, have a high tumor bulk & an indication for treatment, as defined by the Groupe d'Etude des Lymphomes Folliculaires (GELF) criteria.
  3. Eastern Cooperative Oncology Group (ECOG) performance status grade 0-2.
  4. The presence of a molecular marker in bone marrow or peripheral blood for MRD assessment.

Exclusion Criteria:

  1. FL grade IIIb.
  2. HIV infection.
  3. HBsAg positivity.
  4. Active malignancy other than FL
  5. Pregnancy or lactation.

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:Reduced number of bendamustine cycles in patients with mid-induction MRD negativity
Patients with follicular lymphoma treated with obinutuzumab bendamustine & achieving MRD negativity as well as complete metabolic response on PET-CT at mid-induction would continue obinutuzumab treatment while omitting bendamustin after 4 cycles.
Chemotherapy
他の名前:
  • リボムスチン
Immunotherapy
他の名前:
  • ガジバ

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
Progression free survival among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
時間枠:Progression free survival will be assessed 24 months after the end of induction.
Progression-free survival is defined as the time from randomization to the earliest event of progression, relapse, or death from any cause. progression-free survival, is assessed by the investigator.
Progression free survival will be assessed 24 months after the end of induction.

二次結果の測定

結果測定
メジャーの説明
時間枠
Progression of disease within 24 months (POD24)
時間枠:POD24 will be assessed at 24 months after treatment initiation
POD24 is defined as disease progression or death due to disease progression occurring within 24 months after treatment initiation, as assessed by the investigator.
POD24 will be assessed at 24 months after treatment initiation
Overall survival among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
時間枠:Overall survival will be assessed 24 months after the end of induction.
Overall survival is defined as the time from study initiation to death from any cause.
Overall survival will be assessed 24 months after the end of induction.
The rate of MRD negativity persistence at 12 months among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
時間枠:Persistence of MRD negativity will be assessed 12 months after study initiation.
MRD will be assessed at mid-induction, end of induction and subsequently every 6 months.
Persistence of MRD negativity will be assessed 12 months after study initiation.
The proportion of adverse events among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
時間枠:The proportion of various adverse events will be assessed until 24 months from the end of induction.
The proportion of various adverse events will be assessed as documented by the investigator.
The proportion of various adverse events will be assessed until 24 months from the end of induction.

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。

スポンサー

捜査官

  • 主任研究者:Uri Abadi, MD、Meir Medical Center

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)

2020年1月29日

一次修了 (予想される)

2025年8月1日

研究の完了 (予想される)

2025年8月1日

試験登録日

最初に提出

2021年4月8日

QC基準を満たした最初の提出物

2021年6月20日

最初の投稿 (実際)

2021年6月22日

学習記録の更新

投稿された最後の更新 (実際)

2021年6月22日

QC基準を満たした最後の更新が送信されました

2021年6月20日

最終確認日

2021年6月1日

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米国で製造され、米国から輸出された製品。

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