Combination Chemotherapy Followed By Donor Stem Cell Transplant in Treating Patients With Hemophagocytic Lymphohistiocytosis
Hemophagocytic Lymphohistiocytosis
RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of hemophagocytic lymphohistiocytosis cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more hemophagocytic lymphohistiocytosis cells. A donor stem cell transplant may be able to replace blood-forming cells that were destroyed by chemotherapy. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells. Cyclosporine and methotrexate may stop this from happening.
PURPOSE: This phase III trial is studying how well combination chemotherapy followed by a donor stem cell transplant works in treating patients with hemophagocytic lymphohistiocytosis.
調査の概要
状態
条件
詳細な説明
OBJECTIVES:
Primary
- Provide and evaluate revised induction and maintenance therapy comprising etoposide, dexamethasone, and cyclosporine, in terms of achieving and maintaining an acceptable clinical condition in order to perform a curative allogeneic hematopoietic stem cell transplantation (AHSCT), in patients with primary inherited or severe and persistent secondary hemophagocytic lymphohistiocytosis (HLH).
- Evaluate and improve the outcome of AHSCT with various types of donors.
- Determine the prognostic importance of the state of remission at the time of AHSCT.
- Evaluate the neurological complications, in terms of early neurological alterations and cerebrospinal fluid (CSF) findings, in patients treated with this regimen.
Secondary
- Improve the understanding of the pathophysiology of HLH by conducting biological studies of genetics and cytotoxicity in these patients, including genotype-phenotype studies and the prognostic value of natural killer (NK) cell activity subtyping.
OUTLINE: This is a multicenter study.
- Induction therapy (weeks 1-8): Patients receive etoposide IV over 1-3 hours twice weekly in weeks 1 and 2 and then once weekly in weeks 3-8. Patients also receive dexamethasone IV or orally once daily and cyclosporine IV or orally twice daily in weeks 1-8. Patients with clinically evident, progressive neurological symptoms or an abnormal cerebrospinal fluid (CSF) (cell count and protein) that has not improved after 2 weeks of induction therapy undergo intrathecal therapy comprising methotrexate and hydrocortisone once weekly in weeks 3-6.
Patients are evaluated after 8 weeks of induction therapy. Patients with primary (i.e., familial) hemophagocytic lymphohistiocytosis (HLH) or genetic evidence of HLH proceed to maintenance therapy. Patients with severe and persistent secondary (i.e., nonfamilial) HLH and no genetic evidence of HLH proceed to maintenance therapy only if their disease is still active after induction therapy. Patients with nonfamilial HLH and no genetic evidence of HLH who have achieved complete remission (CR) discontinue treatment. If their disease reactivates, they may then proceed to allogeneic hematopoietic stem cell transplantation (AHSCT).
- Maintenance therapy (weeks 9-40): Patients receive dexamethasone IV on days 1-3 in weeks 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, and 40; etoposide IV over 1-3 hours once in weeks 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, and 39; and cyclosporine IV or orally twice daily in weeks 9-40.
After completion of maintenance therapy, patients with primary (i.e., familial) HLH, severe and persistent secondary (i.e., nonfamilial) HLH, or reactivating disease proceed to AHSCT. Patients with nonfamilial HLH who have completed maintenance therapy, but do not go on to receive AHSCT, may be recommended for additional maintenance therapy at the discretion of the treating physician.
AHSCT:
- Preparative regimen: Patients receive a preparative regimen comprising busulfan orally or IV four times daily on days -8 to -5, etoposide IV over 6 hours on day -4, and cyclophosphamide IV over 1 hour on days -3 and -2. Patients who are undergoing unrelated AHSCT, also receive antithymocyte globulin (ATG) IV over 12 hours on days -3 to -1.
- Transplantation: Patients undergo AHSCT on day 0.
- Graft-versus-host disease prophylaxis: Beginning on day -1, patients receive cyclosporine IV continuously and then orally, when tolerated, once daily for 6-12 months. Patients also receive methotrexate* IV on days 1, 3, and 6.
NOTE: *As a substitute for methotrexate, patients may receive oral mycophenolate mofetil twice daily on days 0-40, followed by a taper and discontinuation.
Patients undergo periodic blood collection and bone marrow biopsies for biological studies.
After completion of study treatment, patients are followed periodically for up to 5 years.
PROJECTED ACCRUAL: A total of 288 patients will be accrued for this study.
研究の種類
入学 (予想される)
段階
- フェーズ 3
連絡先と場所
研究場所
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England
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Birmingham、England、イギリス、B4 6NH
- Birmingham Children's Hospital
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Bristol、England、イギリス、BS2 8AE
- Institute of Child Health at University of Bristol
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Cambridge、England、イギリス、CB2 2QQ
- Addenbrooke's Hospital
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Herts、England、イギリス、WD18 0HB
- Watford General Hospital
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Leeds、England、イギリス、LS9 7TF
- Leeds Cancer Centre at St. James's University Hospital
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Liverpool、England、イギリス、L12 2AP
- Royal Liverpool Children's Hospital, Alder Hey
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London、England、イギリス、WC1N 3JH
- Great Ormond Street Hospital for Children
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Manchester、England、イギリス、M27 4HA
- Royal Manchester Children's Hospital
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Sheffield、England、イギリス、S10 2TH
- Children's Hospital - Sheffield
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Southampton、England、イギリス、SO16 6YD
- Southampton General Hospital
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Scotland
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Aberdeen、Scotland、イギリス、AB25 2ZG
- Royal Aberdeen Children's Hospital
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Edinburgh、Scotland、イギリス、EH9 1LF
- Royal Hospital for Sick Children
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Glasgow、Scotland、イギリス、G3 8SJ
- Royal Hospital for Sick Children
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
DISEASE CHARACTERISTICS:
Newly diagnosed hemophagocytic lymphohistiocytosis (HLH) meeting 1 of the following criteria*:
- Diagnosis by molecular/genetic methods
Diagnosis by meeting 5 out of 8 of the following criteria:
Clinical criteria:
- Fever
- Splenomegaly
Laboratory criteria:
Cytopenias affecting ≥ 2 of 3 lineages in the peripheral blood, including the following:
- Hemoglobin < 9.0 g/dL (< 10.0 g/dL in infants < 4 weeks of age)
- Platelet count < 100,000/mm^3
- Neutrophil count < 1,000/mm^3
Hypertriglyceridemia and/or hypofibrinogenemia:
- Fasting triglycerides ≥ 3.0 mmol/L (i.e., ≥ 265 mg/dL)
- Fibrinogen ≤ 1.5 g/L
Histopathologic criteria:
Hemophagocytosis in bone marrow, spleen, or lymph nodes
- No evidence of malignancy
New diagnostic criteria:
- Low or absent natural killer (NK) cell activity
- Ferritin ≥ 500 mcg/L
- Soluble CD25 (i.e., soluble interleukin-2 receptor) ≥ 2,400 U/mL NOTE: *Patients who do not meet the diagnostic criteria for HLH but who have a strong clinical suspicion of HLH may be eligible at the discretion of the investigator
- Primary HLH (i.e., familial hemophagocytic lymphohistiocytosis [FLH]) OR secondary HLH (i.e., severe acquired form of HLH)
Acceptable donor meeting 1 of the following criteria:
- HLA-identical related donor
- Matched unrelated donor
- Mismatched unrelated donor
- Familial haploidentical donor
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- No prior cytotoxic treatment for HLH
- No prior cyclosporine treatment for HLH
研究計画
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
- マスキング:なし(オープンラベル)
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 |
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サバイバル
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協力者と研究者
捜査官
- スタディチェア:Vasanta Nanduri, MD、Watford General Hospital
研究記録日
主要日程の研究
研究開始
一次修了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
- リンパ疾患
- 組織球症、非ランゲルハンス細胞
- 組織球症
- リンパ組織球症、血球貪食
- 薬の生理作用
- 薬理作用の分子機構
- 抗感染剤
- 自律神経剤
- 末梢神経系エージェント
- 核酸合成阻害剤
- 酵素阻害剤
- 抗炎症剤
- 抗リウマチ剤
- 代謝拮抗薬、抗腫瘍薬
- 代謝拮抗剤
- 抗悪性腫瘍薬
- 免疫抑制剤
- 免疫学的要因
- 制吐薬
- 胃腸薬
- グルココルチコイド
- ホルモン
- ホルモン、ホルモン代替物、およびホルモン拮抗薬
- 抗腫瘍剤、ホルモン剤
- 抗悪性腫瘍薬、アルキル化
- アルキル化剤
- 骨髄破壊的アゴニスト
- 抗悪性腫瘍剤、ファイトジェニック
- トポイソメラーゼ II 阻害剤
- トポイソメラーゼ阻害剤
- 皮膚科用薬
- 抗菌剤
- 抗生物質、抗悪性腫瘍薬
- 抗真菌剤
- 生殖制御剤
- 抗結核剤
- 妊娠中絶薬、非ステロイド系
- 中絶エージェント
- 葉酸拮抗薬
- 抗生物質、抗結核薬
- カルシニューリン阻害剤
- デキサメタゾン
- シクロホスファミド
- エトポシド
- メトトレキサート
- ミコフェノール酸
- ブスルファン
- ヒドロコルチゾン
- ヒドロコルチゾン 17-酪酸 21-プロピオン酸
- 酢酸ヒドロコルチゾン
- ヘミコハク酸ヒドロコルチゾン
- 抗リンパ球血清
- シクロスポリン
- シクロスポリン
その他の研究ID番号
- CDR0000481605
- CCLG-LCH-2006-02
- EU-20619
- UKCCSG-HLH-2004
- EUDRACT-2005-002187-28
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