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。

Alemtuzumab, Fludarabine Phosphate, and Total-Body Irradiation Followed by Cyclosporine and Mycophenolate Mofetil in Treating Patients Who Are Undergoing Donor Stem Cell Transplant for Hematologic Cancer

2017年4月25日 更新者:Brenda Sandmaier、Fred Hutchinson Cancer Center

Campath (Alemtuzumab) Dose Escalation, Low-Dose TBI and Fludarabine Followed by HLA Class II Mismatched Donor Stem Cell Transplantation for Patients With Hematologic Malignancies: A Multicenter Trial

This phase II trial is studying the side effects and best dose of alemtuzumab when given together with fludarabine phosphate and total-body irradiation followed by cyclosporine and mycophenolate mofetil in treating patients who are undergoing a donor stem cell transplant for hematologic cancer. Giving low doses of chemotherapy, such as fludarabine phosphate, a monoclonal antibody, such as alemtuzumab, and radiation therapy before a donor stem cell transplant helps stop the growth of cancer cells. Giving chemotherapy or radiation therapy before or after transplant also stops the patient's immune system from rejecting the donor's bone marrow stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after the transplant may stop this from happening.

調査の概要

状態

完了

条件

詳細な説明

PRIMARY OBJECTIVES:

I. To determine which dose of Campath (alemtuzumab) allows related and unrelated human leukocyte antigen (HLA) class-II mismatched hematopoietic cell transplantation (HCT) with an incidence of grade III-IV acute graft-versus-host disease (GVHD) less than 40%.

SECONDARY OBJECTIVES:

I. Incidence of graft rejection.

II. Number of days of steroids >= 1mg/kg required before day 100 in each patient.

III. Incidence of non-relapse mortality.

IV. Risk/incidence of infections.

V. Immune reconstitution.

VI. Risk for disease progression and relapse.

OUTLINE: This is a dose-escalation study of alemtuzumab.

NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab intravenously (IV) over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose total-body irradiation (TBI) on day 0.

ALLOGENEIC PERIPHERAL BLOOD STEM CELL TRANSPLANTATION (PBSCT): After completion of TBI, patients undergo allogeneic PBSCT on day 0.

IMMUNOSUPPRESSION: Patients receive cyclosporine orally (PO) or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD.

After completion of study treatment, patients are followed up periodically for 12 months, at 18 months, and then annually for 5 years.

研究の種類

介入

入学 (実際)

12

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

    • Washington
      • Seattle、Washington、アメリカ、98109
        • Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
      • Torino、イタリア、10126
        • University of Torino

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

74年歳未満 (子、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:

  • The patient must be not eligible for conventional transplants and must have disease expected to be stable for at least 100 days without chemotherapy
  • Patients with hematologic malignancies treatable with HCT will be included:

    • Aggressive non-Hodgkin lymphomas (NHLs) and other histologies such as diffuse large B-cell NHL: not eligible for autologous HCT, not eligible for conventional myeloablative HCT, or after failed autologous HCT;
    • Low grade NHL: with < 6 month duration of complete response (CR) between courses of conventional therapy;
    • Mantle cell NHL: may be treated in first CR;
    • Chronic lymphocytic leukemia (CLL): must have failed 2 lines of conventional therapy and must be refractory to fludarabine; this includes patients who fail to have a complete or partial response after therapy with a regimen containing fludarabine (or another nucleoside analog] or experience disease relapse within 12 months after completing therapy with a regimen containing fludarabine [or another nucleoside analog);
    • Hodgkin's disease (HD): must have received and failed frontline therapy and have failed or were not eligible for autologous transplant;
    • Multiple myeloma (MM): must have received prior chemotherapy or failed autografting; following a planned autologous transplant [tandem] is allowed;
    • Acute myeloid leukemia (AML): must have < 5% marrow blasts at the time of transplant;
    • Acute lymphocytic leukemia (ALL): must have < 5% marrow blasts at the time of transplant;
    • Chronic myelogenous leukemia (CML): patients will be accepted beyond first clinical progression (CP1) if they have received previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
    • Myelodysplastic syndrome/myeloproliferative disease (MDS/MPD): must have failed previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
    • Waldenstrom's macroglobulinemia: must have failed 2 courses of therapy
  • Patient refuses to be treated on a conventional transplant protocol; for this inclusion criteria, transplants must be approved by both the participating institution's patient review committee, such as the Patient Care Conference (PCC) at the Fred Hutchinson Cancer Research Center (FHCRC), and the FHCRC principal investigator
  • Patient with related or unrelated donors for whom:

    • There is a likelihood of disease progression while HLA typing and results of a preliminary search and the donor pool suggest that a 10/10 HLA-A, B, C, DRB1 and DQB1 matched unrelated donor will not be found;
    • Patient and donor must be matched for at least one DRB1 allele and one DQB1 allele;
    • Best available matches are HLA class I HLA-A, -B, -C allele matched donors allowing for any one or two DRB1 and/or DQB1 antigen/allele mismatch;
    • There is no indication for an autologous transplantation as a treatment option
  • DONOR: For HLA matching inclusion criteria, see patient inclusion criteria
  • DONOR: Only peripheral blood stem cells (PBSC) will be permitted as a HSC source on this protocol

Exclusion Criteria:

  • Positive crossmatch between donor and recipients
  • Patient's life expectancy is severely limited by diseases other than malignancy
  • Patient has central nervous system (CNS) involvement with disease refractory to intrathecal chemotherapy
  • Presence of circulating leukemic blasts (in the peripheral blood) detected by standard pathology for patients with AML, ALL or CML
  • Patient is a fertile man or woman unwilling to use contraceptives during and for up to 12 months post treatment
  • Patient is a female who is pregnant or breastfeeding
  • Patient is human immunodeficiency virus (HIV) positive
  • Patients with active non-hematologic malignancies (except non-melanoma skin cancers)
  • Patients with a history of non-hematologic malignancies (except non-melanoma skin cancers) currently in a complete remission, who are less than 5 years from the time of complete remission, and have a > 20% risk of disease recurrence
  • Patient has a fungal infection with radiological progression after receipt of amphotericin B or active triazole for greater than 1 month
  • Patient has the following organ dysfunction:

    • Symptomatic coronary artery disease or ejection fraction < 35% or other cardiac failure requiring therapy; ejection fraction is required if age > 50 years or if the patient has a history of anthracyclines or history of cardiac disease;
    • Diffusion capacity of the lung for carbon monoxide (DLCO) < 35% total lung capacity (TLC) < 35%, forced expiratory volume of the lung in one second (FEV1) < 35% and/or receiving supplementary continuous oxygen; the FHCRC study principal investigator (PI) must approve enrollment of all patients with pulmonary nodules;
    • Liver function abnormalities: patient with clinical or laboratory evidence of liver disease will be evaluated for the cause of liver disease, its clinical severity in terms of liver function, bridging fibrosis, and the degree of portal hypertension; the patient will be excluded if he/she is found to have fulminant liver failure, cirrhosis of the liver with evidence of portal hypertension, alcoholic hepatitis, esophageal varices, a history of bleeding esophageal varices, hepatic encephalopathy, uncorrectable hepatic synthetic dysfunction evinced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal liver abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin > 3mg/dL, or symptomatic biliary disease
  • Patient has poorly controlled hypertension and on multiple antihypertensives
  • Karnofsky performance score < 70 for adult patients
  • Lansky play-performance score < 70 for pediatric patients
  • Patient received cytotoxic agents for "cytoreduction" within three weeks (or the interval in which a cycle of standard chemotherapy would be administered in a non-transplant setting) prior to initiating the nonmyeloablative transplant conditioning; (exceptions are hydroxyurea and imatinib mesylate)
  • DONOR: Marrow donors
  • DONOR: Positive crossmatch between donor and recipient
  • DONOR: Donor is HIV-positive and/or has a medical condition that would result in increased risk for filgrastim (G-CSF) mobilization and harvest of PBSC
  • DONOR: Donor age < 12 years

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:Treatment (chemotherapy, TBI, transplant)

NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab IV over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose TBI on day 0.

ALLOGENEIC PBSCT: After completion of TBI, patients undergo allogeneic PBSCT on day 0.

IMMUNOSUPPRESSION: Patients receive cyclosporine PO or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD.

相関研究
与えられた IV
他の名前:
  • 2-F-ara-AMP
  • ベネフラー
  • フルダーラ
PBSCTを受ける
他の名前:
  • PBPC移植
  • PBSC移植
  • 末梢血前駆細胞移植
  • 移植, 末梢血幹細胞
与えられたPO
他の名前:
  • セルセプト
  • MMF
与えられた IV
他の名前:
  • キャンパス-1H
  • 抗CD52モノクローナル抗体
  • MoAb CD52
  • モノクローナル抗体 Campath-1H
  • モノクローナル抗体 CD52
低用量TBIを受ける
他の名前:
  • TBI
与えられた PO または IV
他の名前:
  • シクロスポリン
  • シクロスポリン A
  • CYSP
  • サンディミューン
同種幹細胞移植を受ける
Undergo GVHD prophylaxis/therapy
他の名前:
  • 予防/治療、移植片対宿主病
  • 予防/治療、GVHD

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
Incidence of Grade III-IV Acute GVHD
時間枠:100 days after transplant

Severity of Individual Organ Involvement

Liver:

Stage 2 - bilirubin (3-5.9mg/100ml) Stage 3 - bilirubin (6-14.9mg/100ml) Stage 4 - bilirubin > 15mg/100ml

Gut:

Diarrhea is graded stage 1 to stage 4 in severity. Nausea and vomiting and/or anorexia caused by GVHD is assigned as stage 1 in severity. The severity of gut involvement is assigned to the most severe involvement noted. Patients with visible bloody diarrhea are at least stage 2 gut and grade 3 overall

Severity of GVHD

Grade III - Stage 2 to 4 gastrointestinal involvement and/or Stage 2 to 4 liver involvement with or without a rash Grade IV - Pattern and severity of GVHD similar to grade 3 with extreme constitutional symptoms or death

100 days after transplant

二次結果の測定

結果測定
メジャーの説明
時間枠
Incidence of Graft Rejection
時間枠:84 days after transplant
Percentage patients that experienced graft rejection.
84 days after transplant
Incidence of High-dose Corticosteroid Utilization.
時間枠:100 days after transplant
Percentage patients requiring steroids greater than 1 mg/kg.
100 days after transplant
Incidence of Non-relapse Mortality
時間枠:100 days after transplant
Percentage patient deaths due to non-relapse mortality
100 days after transplant
Incidence of Infection
時間枠:Up to 5 years post-transplant
Percentage patients that experienced infection(s).
Up to 5 years post-transplant
Immune Reconstitution
時間枠:Up to 1 year post-transplant
The outcome of immune reconstitution was not analyzed by the collaborating laboratory because only a small number of patients were only enrolled in Dose Level 1 (no alemtuzumab). The Dose Level 1 patients were going to be the baseline for which to compare the other patients on Dose Level 2 (and 3) who would have received alemtuzumab. The collaborating investigator determined that the study was not worthwhile performing based on this information.
Up to 1 year post-transplant
Disease Progression/Relapse
時間枠:Up to 5 years

CML New cytogenetic abnormality and/or development of accelerated phase or blast crisis. The criteria for accelerated phase will be defined as unexplained fever greater than 38.3°C, new clonal cytogenetic abnormalities in addition to a single Ph-positive chromosome, marrow blasts and promyelocytes >20%.

AML, ALL >5% marrow blasts by morphologic or flow cytometric, or appearance of extramedullary disease.

CLL ≥1 of: Physical exam/Imaging studies (nodes, liver, and/or spleen) ≥50% increase or new, circulating lymphocytes by morphology and/or flow cytometry ≥50% increase, and lymph node biopsy w/ Richter's transformation.

NHL >25% increase in the sum of the products of the perpendicular diameters of marker lesions, or the appearance of new lesions.

MM

≥100% increase of the serum myeloma protein from its lowest level, or reappearance of myeloma peaks that had disappeared w/ treatment; or definite increase in the size or number of plasmacytomas or lytic bone lesions.

Up to 5 years

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

2005年3月1日

一次修了 (実際)

2010年7月1日

研究の完了 (実際)

2015年5月26日

試験登録日

最初に提出

2005年7月8日

QC基準を満たした最初の提出物

2005年7月8日

最初の投稿 (見積もり)

2005年7月11日

学習記録の更新

投稿された最後の更新 (実際)

2017年5月30日

QC基準を満たした最後の更新が送信されました

2017年4月25日

最終確認日

2017年4月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 1959.00 (その他の識別子:Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium)
  • P30CA015704 (米国 NIH グラント/契約)
  • NCI-2009-01496 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
  • P01CA018029 (米国 NIH グラント/契約)

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