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TerminatedNCT02374424GIOTTOUpdated Jun 6, 2022

Phase II Study With Ga101-DHAP as Induction Therapy in Relapsed/Refractory DLBCL Patients

A Phase 2 interventional study of GA101_DHAP in Diffuse, Large B-Cell, Lymphoma, sponsored by Fondazione Italiana Linfomi - ETS. Terminated at 10 sites in Italy. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-06-06.

Sponsored by Fondazione Italiana Linfomi - ETS · Phase 2, Interventional, and Treatment

Why this study was terminated
Interim analysis planned as per protocol didn't provide positive outcome therefore enrollment was not reopened. However, the enrolled patients concluded therapy and continued into the follow-up phase. The study was closed only after LVLP.

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Nov 2014, registered Feb 2015).
Phase
Phase 2
Study type
Interventional
Enrollment
29
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
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Study summary

Aim of this trial is to assess the efficacy of new anti-CD20 antibody (GA101) in association with DHAP as induction therapy before high dose chemotherapy BEAM with ASCT in patients with relapsed/refractory DLBCL.

Read the detailed description

This is a prospective, multicenter, single arm, phase II trial in young patients (18-65 years) affected by relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) at diagnosis,eligible to high-dose therapy.

Aim of the study is to assess whether the addition of GA101 to DHAP is more promising than standard R-DHAP, as induction therapy before high dose chemotherapy BEAM with ASCT with respect to response.

The study is designed primarily to evaluate the efficacy of GA101-DHAP in patients with DLBCL who have relapsed or are refractory to one chemotherapy regimen and secondarily to assess safety and capability to mobilize peripheral stem cells The study is designed with two stages and with stopping rules after the first stage. In particular, at the end of the first stage, the study will be stopped if the efficacy is too low or if the toxicity, measured during the drug administration period, is too high with respect to pre-defined thresholds. .

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Conditions studied

  • Diffuse, Large B-Cell, Lymphoma
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In context

Lymphoma

5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.

This study's enrollment of 29 is below the median of 40 across 4,508 interventional studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

Fondazione Italiana Linfomi - ETS is the lead sponsor of 89 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. 18≥ Age \< 65
  2. Relapsed/refractory disease after receiving one line of standard R-CHOP like chemotherapy
  3. Diffuse Large B-cell Lymphoma at relapse. The re-biopsy is particularly recommended if relapse is over 1 year from previous complete remission. If this is harmful for the patient, the patient can be enrolled if archival tumor sample and block from first diagnosis are available.
  4. Measurable and/or evaluable disease
  5. Any Ann Arbor stage and IPI group at relapse
  6. Performance status \< 2 according to Eastern Cooperative Oncology Group (ECOG) scale unless due to lymphoma
  7. No Central Nervous System (CNS) disease (meningeal and/or brain involvement by lymphoma)
  8. Adequate haematological counts: Absolute Neutrophil Count (ANC) > 1.5 x 109/L, Hgb > 10.5 g/dl (transfusion independent), Platelet count > 75 x 109/L (transfusion independent), with the exception of cytopenia due to lymphoma bone marrow involvement
  9. Normal liver function (ALP, AST, ALT, GGT, conjugated bilirubin total \< 2 x ULN) if not related to lymphoma
  10. Normal kidney function (creatinine clearance >= 80 ml/min)
  11. Cardiac ejection fraction > 50% (MUGA scan or echocardiography)
  12. Normal lung function
  13. Absence of active infections
  14. Non peripheral neuropathy or active neurological non neoplastic disease of CNS
  15. Non major surgical intervention prior 3 months to randomization if not due to lymphoma and/or not other disease life-threatening that can compromise chemotherapy treatment
  16. Disease free of prior malignancies other than lymphoma for > 3 years with exception of currently treated squamous cell and basal cell carcinoma of the skin or carcinoma in situ of the cervix or breast
  17. Life expectancy > 6 months
  18. No psychiatric illness that precludes understanding concepts of the trial or signing ten informed consent
  19. Written informed consent
  20. Women must be:

    1. postmenopausal for at least 1 year (must not have had a natural menses for at least 12 months)
    2. surgically sterile (have had a hysterectomy or bilateral oophorectomy, tubal ligation, or otherwise be incapable of pregnancy),
    3. abstinent (at the discretion of the investigator/per local regulations), or
    4. if sexually active, be practicing a highly effective method of birth control (eg, prescription oral contraceptives, contraceptive injections, contraceptive patch, intrauterine device, double-barrier method (eg, condoms, diaphragm, or cervical cap, with spermicidal foam, cream, or gel, male partner sterilization) as local regulations permit, before entry, and must agree to continue to use the same method of contraception throughout the study. They must also be prepared to continue birth control measures for at least 18 months after terminating treatment.
  21. Women of childbearing potential must have a negative serum or urine beta-human chorionic gonadotropin (beta-hCG) pregnancy test at screening
  22. Men must agree to use an acceptable method of contraception (for themselves or female partners as listed above) for the duration of the study. Men must agree to use a double barrier method of birth control and to not donate sperm during the study and for 3 months after receiving the last dose of study drug.

Exclusion criteria

Exclusion Criteria:

  1. Diagnosis of Lymphoblastic Lymphoma, Burkitt Lymphoma, Non Hodgkin Lymphoma CD20 negative, Mantle Cell Lymphoma, Follicular Lymphoma, Primary Mediastinal Lymphoma
  2. Age ≥ 65 years
  3. Patients ineligible to high-dose chemotherapy
  4. Performance status > 2 according to ECOG scale if not due to lymphoma
  5. Patients who previously received GA101 (obinutuzumab) are excluded.
  6. Patient has known or suspected hypersensitivity or intolerance to Rituximab
  7. Patient has received an experimental drug or used an experimental medical device within 4 weeks before the planned start of treatment. Concurrent participation in nontreatment studies is allowed, if it will not interfere with participation in this study.
  8. CNS disease (meningeal and/or brain involvement by lymphoma)
  9. History of clinically relevant liver or renal insufficiency; significant cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, rheumatologic, hematologic, psychiatric, or metabolic disturbances
  10. Positive test results for chronic hepatitis B infection (defined as positive HBsAg serology). Patients with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if HBV DNA is undetectable. These patients must be willing to undergo monthly DNA testing.
  11. Positive test results for hepatitis C (HCV antibody serology testing). Patients positive for HCV antibody are eligible only if PCR is negative for HCV RNA.
  12. Known history of HIV seropositive status. For patients with unknown HIV status, HIV testing will be performed at screening if required by local regulations.
  13. Uncontrolled diabetes (if receiving antidiabetic agents, subjects must be on a stable dose for at least 3 months before first dose of study drug
  14. Uncontrolled or severe cardiovascular disease including myocardial infarction within six months of enrollment, New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, clinically significant pericardial disease, or cardiac amyloidosis
  15. Cardiac ejection fraction \< 45% (MUGA scan or echocardiography)
  16. Creatinine clearance \< 45 ml/min
  17. Presence of major neurological disorders
  18. Active infection
  19. Major surgical intervention prior 3 months to randomization if not due to lymphoma and/or other disease life-threatening that can compromise chemotherapy treatment
  20. Prior malignancies other than lymphoma in the last 3 years with exception of currently treated squamous cell and basal cell carcinoma of the skin or carcinoma in situ of the cervix or breast
  21. Life expectancy \< 6 months
  22. Any other coexisting medical or psychological condition that would preclude participation in the study or compromise ability to give informed consent.
  23. If female, the patient is pregnant or breast-feeding.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
29 participants (actual)

Study arms

  • Experimental
    GA101_DHAP

    Patients receive: GA101-DHAP x 2, restaging, mobilization and collection of peripheral blood stem cells, + GA101-DHAP x 2, restaging with PET and CT and consolidation with BEAM and ASCT in patients in response (CR+PR). During the treatment period of four cycles, all patients will receive a total of four 28-day courses of chemotherapy.

    Drug: GA101_DHAP

Interventions

  • DrugGA101_DHAP

    Aim of the study is to assess whether the addition of GA101 to DHAP is more promising than standard R-DHAP, as induction therapy before high dose chemotherapy BEAM with ASCT with respect to response. Scheme of treatment: * GA101 1000 mg iv day 1, 8, 15 on first cycle (starting from cycle 2, GA101 1000 mg day 1) * Cisplatin 100 mg/sqm iv day 1 of every cycles in 24-hours infusion * Cytarabine 2000 mg/sqm in 3-hours infusion every 12 hours iv day 2 of every cycles * Dexamethasone 40 mg day 1-4 of every cycles * Pegfilgrastim 6 mg sc single dose 24 hours after the end of chemotherapy or G-CSF from day 4 till stem cell harvest during mobilization's course (II o III cycle GA101-DHAP) * GA101 1000 mg iv 24 hours before apheresis as purging in vivo during second courses of therapy

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What researchers measure

Primary outcomes

  1. Aim of this trial is to assess the efficacy of new anti-CD20 antibody (GA101) in association with DHAP as induction therapy before high dose chemotherapy BEAM with ASCT in patients with relapsed/refractory DLBCL.

    Primary objective is to assess whether the treatment achieves an absolute increase of the CR proportion of at least 20% (from 30% to 50%) with respect to the standard treatment. The complete response rate (CR) evaluated by PET scan after four cycles of GA101-DHAP before ASCT according to Cheson criteria.

    Time frame: 4 months

Secondary outcomes

  1. Overall Response Rate (ORR) prior to consolidation with BEAM and ASCT

    A patient is defined as a responder if she/he has a complete or partial response, evaluated by PET/TC, after four cycles of GA101-DHAP

    Time frame: 2 years

  2. Progression free survival (PFS) at 6 month after the end of treatment (EOT)

    Measured from the date of starting salvage therapy to the date of disease progression, relapse or death from any cause. Responding patients and patients who are lost to follow up will be surveyed at their last assessment date.

    Time frame: 6 month

  3. Overall Survival (OS) at 2 years after the EOT

    Measured from the date of starting salvage therapy to the date of death from any cause. Patients alive at the time of the final analysis will be surveyed at the date of the last contact. For both PFS and OS minimum follow up time required for all patients will be 2 years.

    Time frame: 2 years

  4. Toxicity: Severe, life-threatening, fatal (grade 3, 4 and 5) and/or serious adverse events

    Severe, life-threatening, fatal (grade 3, 4 and 5) and/or serious adverse events are defined according to "Common Terminology Criteria for Adverse Events" (CTCAE), version 4.0. and adverse events of special interests (AESI)

    Time frame: 2 years

  5. The hematopoietic cell mobilization

    Mobilizing potential: amount of CD34 + stem cell collected /Kg

    Time frame: 2 years

  6. Feasibility: the rate of patients actually proceeding to ASCT

    Proportion of patients successfully completing ASCT

    Time frame: 2 years

07

Study locations

10 sites
  • Ospedale San Bortolo
    Vicenza, VI 36100, Italy
  • Ospedale di Bolzano, Reparto di Ematologia & CTMO
    Bolzano, 39100, Italy
  • A.O. Universitaria Careggi
    Firenze, 50139, Italy
  • Ospedale dell'Angelo, U.O. Ematologia
    Mestre, 30174, Italy
  • A.O. Universitaria Policlinico Di Modena
    Modena, 41124, Italy
  • Ematologia Policlinico San Matteo
    Pavia, 27100, Italy
  • AO di Perugia S. Maria della misericordia
    Perugia, 06132, Italy
  • Ematologia Ospedale S.Camillo Forlanini
    Roma, 00149, Italy
  • Policlinico Umberto I - Università "La Sapienza"
    Roma, 00161, Italy
  • Ematologia e Trapianto Istituto Regina Elena IFO
    Roma, Italy
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References and documents

Study documents

  • Protocol and statistical analysis plan · Sep 9, 2016

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02374424
Lead sponsor
Fondazione Italiana Linfomi - ETS
Responsible party
Sponsor
First posted
Feb 27, 2015
Start date
Nov 5, 2014
Primary completion
Feb 2018
Completion
Jun 23, 2020
Last update
Jun 6, 2022

Study contacts

Maurizio Martelli, MD
principal investigator · Dipartimento di Biotecnologie Cellulari ed Ematologia, "La Sapienza" Roma

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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