Stem Cell Factor (SCF) Priming of Haematopoietic Stem Cell Grafts in Malignant Lymphoma (SCF980266)

Aalborg University Hospital

Status and phase

Terminated

Phase 2

Conditions

Malignant Lymphoma

Treatments

Drug: Chemotherapy plus Filgrastim

Drug: r-metHuSCF and Filgrastim

Study type

Interventional

Funder types

Other

NETWORK

Industry

Identifiers

NCT01016795

H-KA-99040-GMS (Other Identifier)

SCF 980266

Details and patient eligibility

About

Clinical Hypothesis:

It is expected that by removing chemotherapy and adding ancestim to the mobilization scheme in most of the subjects sufficient PBPC will be harvested with a minimum of toxicity and side effects.

Full description

Autologous stem cell transplantation is used to support high dose chemotherapy in haematological malignancies.1-2 Peripheral blood progenitor cells (PBPC) have replaced bone marrow cells as the preferred source for transplantation due to faster blood cell recovery.3-4 One variable of major impact for posttransplant care is the number of PBPC harvested.5-8 Therefore, several clinical studies have aimed to identify priming regimens that improve progenitor and stem cell mobilizations and collections without increased toxicity. Frequently, Filgrastim (r-met HuG-CSF) is administrated alone; however, Filgrastim combined with chemotherapy has proven more effective in context of CD34+ cell numbers harvested9-11 and this combination is considered the gold standard for priming and stem cell mobilization in relapsed malignant lymphoma.

Stem cell factor (SCF) is a glycoprotein growth factor that acts on haematopoietic blood cell progenitors.12 Whereas SCF alone exerts little colony-stimulating activity on normal human bone marrow cells in vitro, combination of SCF with other recombinant haematopoietic cytokines results in a synergistic increase in numbers of colonies.13 In vivo, the addition of SCF to G-CSF (Filgrastim) synergistically increases PBPC mobilization compared to Filgrastim alone.14-17 Several clinical trials have reported the ability of the combination of SCF with Filgrastim to mobilize PBPC in patients with lymphoma, multiple myeloma, breast and ovarian cancers even in heavily pretreated patients.18-26 Priming using chemotherapy is toxic and costly11 and new priming procedures need to be established, which is the background for this randomized pilot study. The hypothesis is that elimination of chemotherapy from the priming regimen may decrease the overall toxicity and the ability to collect a sufficient autograft which, however, may be circumvented by adding r-metHuSCF (Ancestim) to the priming regimen. The aim of this randomized phase II trial was to evaluate safety, toxicity and efficacy of growth factors in lymphoma patients considered candidates for high dose chemotherapy.

Enrollment

32 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects with Hodgkin's disease and non-Hodgkin lymphomas (Real classification)
- in relapse
- refractory to initial chemotherapy
- with partial response after initial therapy
Age > 18 years and < 65 years
ECOG performance status 0, 1 or 2
Life expectancy of > 6 months with treatment
ANC > or equal to 1.5 x 109/L, Platelets > or equal to 100 x 109/L
Serum creatinine < or equal to 150 µmol/L, bilirubin, aspartate aminotransferase (ASAT), and alanine aminotransferase (ALAT) less than twice the upper limit defined at the investigating laboratory
Prior to mobilization chemotherapy subject has given written informed consent, personally dated

Exclusion criteria

Prior DexaBEAM or miniBEAM therapy and prior bone marrow or PBPC transplant
Any history of seasonal or recurrent asthma within the preceding 10 years.
Any history of anaphylactic / anaphylactoid-type event manifested by disseminated urticaria, laryngeal oedema, and / or bronchospasm (example, food, insect bites, etc.). Subjects with drug allergies, manifested solely by rash and / or urticaria, are not excluded
Any history of angioedema or recurrent urticaria
Clinical or microbiological evidence of infection at the date of enrollment.
Subjects with a concurrent malignancy
Significant non-malignant disease including documented HIV infection, uncontrolled hypertension, unstable angina, congestive heart failure, poorly controlled diabetes, coronary angioplasty within six months, myocardial infarction within the last six months, or uncontrolled atrial or ventricular cardiac arrhythmias
Pregnant or breast feeding subjects or those of child-bearing potential who are not using adequate contraceptive precautions
Concurrent enrollment on any other protocol using an investigational drug
Haematopoietic growth factors administered within one week of study entry
Subjects with a psychiatric, addictive or any disorder which compromises ability to give truly informed consent for participation in this study
Known sensitivity to E. coli derived products
Concurrent use of beta adrenergic blocking agents

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

32 participants in 2 patient groups

r-metHuSCF and Filgrastim

Active Comparator group

Description:

Patients were randomized in a 1:1 ratio to either chemotherapy combined with 10 µg/kg/d Filgrastim (control arm B), administered by subcutaneous injection for 14 days, or the combination of 10 µg/kg/d Filgrastim and SCF administered subcutaneously at a dose of 20 µg/kg/d (experimental arm A) for 8 days. Different injection sites were used for each cytokine.

Treatment:

Drug: Chemotherapy plus Filgrastim

Drug: r-metHuSCF and Filgrastim

Cyclophosphamide and Filgrastim

Active Comparator group

Description:

Treatment:

Drug: Chemotherapy plus Filgrastim

Drug: r-metHuSCF and Filgrastim