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Prospective, Multicentric, Phase II Randomized Controlled Trial on Two Parallel Groups Comparing the Efficacy of Two Immunosuppressive Drugs (Methotrexate, Cyclophosphamide) in Large Granular Lymphocytes Leukemia

Phase 2
Active, not recruiting
Conditions
Large Granular Lymphocytes Leukemia
Interventions
Registration Number
NCT01976182
Lead Sponsor
Rennes University Hospital
Brief Summary

LGL leukemia represents a rare subtype of chronic T or NK lymphoproliferative disorders. It is an indolent disease, the main hematological or autoimmune complications lead to a treatment in more than 60% of patients.

Investigators set up at the University Hospital of Rennes, a database of more than 300 patients with LGL leukemia from major French services that support this disease, and published in 2010 the largest series of patients in the world (n = 229). However, the limited heterogeneity and retrospective data collected, as all previously released, makes it difficult the proposal of consensual treatment options. If first and second line treatments are based on the use of immunosuppression with methotrexate, cyclophosphamide, or cyclosporin A, no molecule has proven superiority over others. Methotrexate and cyclophosphamide are mainly used in the first line. Invetigators just have in the literature data on about 100 patients treated with either of these drugs. Combining the results of our series with those in the literature, invetigators estimate the respective overall response rate (RG) and complete response rate (CR) in 55% and 30% for methotrexate, and 60% and 50% for cyclophosphamide.

Thus, there are four objective in this study :

1. to compare the respective efficacies of methotrexate and cyclophosphamide when administered as first-line therapies in patients suffering from T/NK LGL leukemia with severe neutropenia or neutropenia associated with infections, and/or anemia requiring transfusions, and/or auto-immune associated disease

2. to evaluate the percentage of patients refractory to methotrexate or cyclophosphamide for which a second line treatment is efficacious

3. to explore, in case of non-response to the first-line therapy, the efficacy of ciclosporine A, the comparison being performed with the treatment which was not administered in the first-line therapy

4. to evaluate the response rate according to the phenotypic subtype of LGL leukemia.

Detailed Description

Large Granular Lymphocyte (LGL) leukemia is a clonal disorder involving tissue invasion of marrow, spleen and liver. Clinical presentation is dominated by recurrent infections associated with neutropenia, anemia, splenomegaly, and auto-immune diseases, particularly rheumatoid arthritis. Both T cell and NK cell subtypes of LGL leukemia are indolent disease and considered as a chronic illness and lead to a treatment in more than 60% of patients.

LGL leukemia displays a chronic clinical course. Recommendations regarding therapy are similar for both subtypes. Indications for treatment include 1) severe neutropenia (ANC \<500 mm3); 2) neutropenia (ANC \<1500mm3) with symptomatic recurrent infections; 3) symptomatic or transfusion-dependent anemia and 4) associated autoimmune conditions requiring therapy, most often rheumatoid arthritis.

There is no standard treatment for patients with LGL leukemia. The numerous case reports published do not provide a consensus for a particular treatment. All the six largest series published in the literature so far (collecting data on more than 40 patients) are retrospective.

Immunosuppressive therapy remains the foundation of treatment including single three agents i.e. methotrexate, oral cyclophosphamide and ciclosporin A. However prospective trials involving large numbers of patients have not been performed and no molecule has proven superiority over others.

Invetigators set up at the University Hospital of Rennes, a database of more than 300 patients with LGL leukemia from major French services that support this disease, and published in 2010 the largest series of patients in the world (n = 229). However, the limited heterogeneity and retrospective data collected, as all previously released, makes it difficult the proposal of consensual treatment options. Combining the results of our series with those of the literature, invetigators estimate that overall response rate and complete response rate are 55% and 30% with methotrexate, 60% and 50% with cyclophosphamide, and 55% and less than 20% with ciclosporine A, respectively.

Thus, there are four objective in this study :

1. to compare the respective efficacies of methotrexate and cyclophosphamide when administered as first-line therapies in patients suffering from T/NK LGL leukemia with severe neutropenia or neutropenia associated with infections, and/or anemia requiring transfusions, and/or auto-immune associated disease

2. to evaluate the percentage of patients refractory to methotrexate or cyclophosphamide for which a second line treatment is efficacious

3. to explore, in case of non-response to the first-line therapy, the efficacy of ciclosporine A, the comparison being performed with the treatment which was not administered in the first-line therapy

4. to evaluate the response rate according to the phenotypic subtype of LGL leukemia.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
166
Inclusion Criteria
  • Common criteria of LGL leukemia: the diagnosis is based on a chronic LGL peripheral blood expansion (>0.5x109/L), usually lasting more than 6 months

  • Specific criteria for T-LGL leukemia or NK-LGL lymphocytosis or chronic NK-LGL leukemia:

    • Specific criteria for T-LGL leukemia:
  • Expression of LGL surface markers compatible with an activated T-cell (commonly alpha-beta+/CD3+/CD8+/CD57+ and/or CD16+) phenotype or gamma-delta+ T cells;

  • Clonal rearrangement of TCRγ gene using PCR or specific and clonal Vβ expression using FCM.

    • Specific criteria for NK-LGL lymphocytosis or chronic NK LGL leukemia:
  • Expression of LGL surface markers compatible with a NK cell (commonly CD3-/CD8+/CD16+ and/or CD16+/CD56+) phenotype;

  • CD56+ or CD16+ NK cells greater than 0.75x109/L;

  • The term of chronic NK-LGL lymphocytosis is used for patients with chronic illness (NB: patients with massive tissue LGL infiltration of the spleen, liver and bone marrow and presenting aggressive clinical behavior are considered as having aggressive NK-LGL leukemia and should not be included).

  • Age above 18 years

  • ECOG performance status of 0-2

  • Life expectancy of at least 1 year

  • Lack of previous treatment (except with G-CSF or transfusions)

  • At least one indication of treatment:

    • Isolated severe neutropenia (ANC <0.5x109/L) or neutropenia (ANC <1.5x109/L) with two or more infections requiring antibiotics;
    • Anemia (whatever the underlying mechanism: pure red cell aplasia or marrow infiltration) requiring transfusions greater than 2 units for two months prior to inclusion, or symptomatic anemia (hemoglobin <10g/dl) with impairment of the quality of life;
    • Associated complications such as systemic diseases or auto-immune diseases (i.e. recurrent uveitis, cutaneous vasculitis, autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura, rheumatoid arthritis resistant to steroids and/or immunomodulator agents (colchicin, disulone, hydrochloroquine)) and justifying a treatment with methotrexate or cyclophosphamide
  • Written informed consent

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Exclusion Criteria
  • Inability to understand or to follow study procedures
  • Prior or concurrent malignancy within the past 5 years except inactive nonmelanomatous skin cancer or carcinoma in situ of the cervix
  • Other serious medical illnesses, such as hepatic, renal, cardiac, pulmonary, neurologic, or metabolic disease that would preclude the patient's ability to tolerate methotrexate, cyclophosphamide, or ciclosporine A
  • Reactive LGL lymphocytosis (i.e. after viral infection)
  • ALAT/ASAT or alkalin phosphatases >3 times normal values
  • Creatinine clairance <50 ml/min
  • Serologic evidence of HIV, hepatitis C or hepatitis B infection
  • Non effective contraception
  • Positive pregnancy test
  • Nursing woman
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
METHOTREXATEMethotrexateIn step 1, 55 patients will receive methotrexate 10mg / m² orally once a week, (at split doses of 5 mg/m2 in the morning and 5 mg/m2 at night), that is to say 2 tablets of 2.5 mg at each take In step 2, responders at Month 4 (CR or PR) will be treated during 8 additional months with methotrexate at the same dosage. Non responders at Month 4 will be randomized and treated either by: * Cyclophosphamide delivered at 100 mg orally once daily, that is to say 2 tablets of 50 mg at each take between Month 5 and Month 8, decreased to 50 mg orally once daily beyond Month 8 for responders at Month 8; * Ciclosporine A delivered at 3 mg/kg per day (at split doses of 1.5 mg/kg in the morning and 1.5 mg/kg at night) orally administered.
CYCLOPHOSPHAMIDECyclophosphamideIn step 1, 55 patients will receive cyclophosphamide 100 mg orally once daily, that is to say 2 tablets of 50 mg at each take. In step 2, responders at Month 4 (CR or PR) will be treated during 8 additional months with cyclophosphamide (at 50 mg orally once daily); Non responders at Month 4 will be randomized and treated either by: * Methotrexate administered at 10 mg/m2 orally once a week (at split doses of 5 mg/m2 in the morning and 5 mg/m2 at night), that is to say 2 tablets of 2.5 mg at each take; * Ciclosporine A delivered at 3 mg/kg per day (at split doses of 1.5 mg/kg in the morning and 1.5 mg/kg at night) orally administered.
Primary Outcome Measures
NameTimeMethod
Complete response (CR)at Month 4

The main endpoint will be the hematological CR rate evaluated after 4 months of treatment (binary endpoint). Complete response (CR) is defined as a normalization of clinical examination (disappearance of splenomegaly) and a complete normalization of blood counts (i.e., hemoglobin \>12g/dL, platelets \>150x109/L, ANC \>1.5x109/L), lymphocytosis \<4x109/L and circulating LGL in the normal range (\<0.3x109/L). The number of LGL will be quantitated on blood smears.

Secondary Outcome Measures
NameTimeMethod
overall response rate (ORR)at Month 4, and at Month 8 and Month 12 in non-responders at Month 4

Hematological overall response rate (ORR) defined as the sum of complete responses and partial responses over the total number of patients.

Time-to-relapsefrom Month 8 to endpoint (in second-line treatment responders)

Time-to-relapse (censored variable). Relapse is defined as re-occurrence of either neutropenia or anemia (ANC \<1x109/L and/or hemoglobin \<10g/dL) or clonal LGL \>0.5x109/L in complete responders, or as a return to baseline values of either ANC or hemoglobin in partial responders, at two monthly consecutive blood tests.

ComplianceMonth 2, Month 4, Month 6, Month 8, Month 10, Month 12

Compliance

Progressive diseaseat Month 4, Month 8 and Month 12

Progressive disease defined as worsening of cytopenia or organomegaly or incidence of infections.

Molecular remissionat Month 4 and Month 12 for hematological complete responders

Molecular remission defined as the disappearance of the clonal pattern of TCR gamma multiplex rearrangement and Phenotypic remission is defined as :

* For the T subtype: disappearance of the excess of CD3+/CD8+ cells (or disappearance of the LGL clone according to the specific subtype observed at inclusion);

* For the NK subtype: disappearance of the excess of CD3-/CD56+ cells (or disappearance of the LGL clone according to the specific subtype observed at inclusion)

Adverse events rateMonth 2, Month 4, Month 6, Month 8, Month 10, Month 12

Adverse events rate

relationship between the response to treatment and the phenotypic subtypeDay 1

Identification of a relationship between the response to treatment and the phenotypic subtype characterized by the panel of monoclonal antibodies defined in the ancillary study subsection.

Complete response (CR)at Month 8 and Month 12

Complete response (CR) is defined as a normalization of clinical examination (disappearance of splenomegaly) and a complete normalization of blood counts (i.e., hemoglobin \>12g/dL, platelets \>150x109/L, ANC \>1.5x109/L), lymphocytosis \<4x109/L and circulating LGL in the normal range (\<0.3x109/L). The number of LGL will be quantitated on blood smears.

Hematological partial response (PR)at Month 4, Month 8 and Month 12

Hematological partial response (PR) defined as an improvement in blood counts which do not meet criteria for complete remission (e.g., ANC increasing more than 50% and reaching more than 0.5 but less than 1.5x109/L with non-recurrence of infections, or hemoglobin level increasing more than 2 g/dL from baseline and transfusion requirements stopping without normalization of the hemoglobin level defined as hemoglobin \>12g/dL).

Trial Locations

Locations (58)

Hematology Service - CH de la cote basque

🇫🇷

Bayonne, France

Hematology Unit - Hopital Saint Louis

🇫🇷

Paris, France

Hematology Unit CHRU Lille

🇫🇷

Lille, France

Hematology Unit - CH Becquerel

🇫🇷

Rouen, France

Hematology Unit CH E.MULLER

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Mulhouse, France

Internal Medicine - CHU Hotel Dieu

🇫🇷

Nantes, France

Hopital Inter-Armées Percy

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Clamart, France

Hematology Service - CH de Brest

🇫🇷

Brest, France

Hematology Unit CHD Vendée

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La Roche sur Yon, France

Hematology Unit CHU Dupuytren

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Limoges, France

hematology Service - CH Louis Pasteur

🇫🇷

Chartres, France

Centre Hospitalier de Cholet

🇫🇷

Cholet, France

Hematology Service - CHU of Rennes

🇫🇷

Rennes, France

Hematology Service CHSF

🇫🇷

Corbeil Essonnes, France

Hematology Unit CH René DUBOS

🇫🇷

Pontoise, France

CHU Henri Mondor Lymphoid Hemopathy Unit

🇫🇷

Creteil, France

Hematology Unit CHU La Conception

🇫🇷

Marseille, France

hematology Unit CHU Caremeau

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Nimes, France

Hematology Unit - CHR Orleans

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Orleans, France

Hematology Unit - Institut Paoli-Calmettes

🇫🇷

Marseille, France

Oncology Unit CH Antoine Lacassagne

🇫🇷

Nice, France

Hematology Service - Hopital La Pitié Salpetrière

🇫🇷

Paris, France

Hematology Unit - Hopital Hotel Dieu

🇫🇷

Paris, France

Hematology Unit Hopital Saint Jean

🇫🇷

Perpignan, France

CH Annecy - Hematology Service

🇫🇷

Pringy, France

CH Saint Quentin Oncohematology

🇫🇷

Saint Quentin, France

Oncology Unit - Institut de cancérologie de la Loire

🇫🇷

Saint Priest en Jarez, France

Hematology Unit CHU Toulouse

🇫🇷

Toulouse, France

Hematology Unit CHU Bretonneau

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Tours, France

Intern Medecine Unit CHBA

🇫🇷

Vannes, France

AP-HP Hôpital Necker - Enfants Malades

🇫🇷

Paris, France

Hematology Unit - Hopital Saint Antoine

🇫🇷

Paris, France

CHU Angers

🇫🇷

Angers, France

CHU Sud

🇫🇷

Amiens, France

Hematology Service - CH Avignon

🇫🇷

Avignon, France

Intern medecine Service - CH Antibes-Juan-les-Pins

🇫🇷

Antibes, France

Hematology Service - CH Beziers

🇫🇷

Beziers, France

Hematology Service - CH Jean Minjoz

🇫🇷

Besançon, France

hematology service - CH Beauvais

🇫🇷

Beauvais, France

Hematology Unit - HOpital Avicienne

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Bobigny, France

Hematology Service - CH Docteur Duchenne

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Boulogne sur Mer, France

Hematology Service - CH François Baclesse

🇫🇷

Caen, France

Hematology Unit CH LE MANS

🇫🇷

Le Mans, France

Hematology Service - Civils hospital

🇫🇷

Colmar, France

hematology Service - CHU Estaing

🇫🇷

Clermont-Ferrand, France

Hematology Unit CH Michalon

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Grenoble, France

CH Robert Boulin

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Libourne, France

CH de Bretagne Sud

🇫🇷

Lorient, France

Hematogy Unit CHU ST ELOI

🇫🇷

Montpellier, France

Hematology Unit CH Notre Dame Bon Secours

🇫🇷

Metz, France

Hematology Unit CH Meaux

🇫🇷

Meaux, France

Hematology Service- CH Haut Leveque

🇫🇷

Pessac, France

Hematology Unit CHU La Miletrie

🇫🇷

Poitiers, France

Hematology Unit CH LYON SUD

🇫🇷

Pierre Benite, France

Hematology Unit- Hopital Robert Debré

🇫🇷

Reims, France

Hôpital André Mignot Centre Hospitalier de Versailles

🇫🇷

Versailles, France

CH Yves Lefoll

🇫🇷

Saint-Brieuc, France

Hematology Unit Hopitaux de Brabois

🇫🇷

Vandoeuvre les Nancy, France

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