Bortezomib-based Regimen for Refractory or Relapsed Acute Lymphoblastic Leukemia

Sponsor

Instituto do Cancer do Estado de São Paulo (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT06034561

Collaborator

Libbs Farmacêutica LTDA (Industry)

Enrollment

Location

Arm

Anticipated Duration (Months)

0.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a interventional phase II study aiming to examine the complete response rate of a bortezomib-based salvage regimen in adults with refractory or relapsed acute lymphoblastic leukemia (ALL), seeking to compare outcomes with the available literature and with our historical data on relapsed/refractory ALL.

Condition or Disease	Intervention/Treatment	Phase
Acute Lymphoblastic Leukemia, in Relapse Acute Lymphoblastic Leukemia With Failed Remission	Drug: Bortezomib	Phase 2

Detailed Description

Acute lymphoblastic leukemia (ALL) is a rare neoplasm in adults, with long-term survival rates approaching 50% with current regimens. Although high rates of complete response are achieved with the first-line therapy, many patients are primary refractory or may further relapse. Arguably, these patients have a more resistant disease with higher risk genetic alterations and a much less likely to be cured, which almost always only can be obtained by a following allogeneic hematopoietic stem-cell transplantation (HSCT). Therefore, strategies to salvage patients with detectable disease after induction blocks or with relapsed disease are crucial to prolong survival and potentially cure those patients, working as a bridge therapy to HSCT. Historically, patients with relapsed/refractory ALL have received multidrug regimens based on high-dose cytarabine, such as fludarabine, cytarabine and idarubicin (FLAG-IDA). Those regimens provide a 30-40% complete response rate with non-negligible toxicity. Recently, new targeted agents such as blinatumomab, inotuzumab, and cellular therapies have arisen for B-lineage disease, even though these agents are not available in the public health setting. Previous studies have tested salvage regimens for ALL encompassing proteasome inhibitors plus highly synergistic drugs (dexamethasone, vincristine, asparaginase, doxorubicin), with exciting outcomes in limited case series. For adults, these regimens are less studied. However, preliminary data suggest that they are less toxic and more potent since patients can receive different drug combinations that they had not been exposed to before. The primary objective of this study is to examine the complete response rate of this regimen in our population, aiming to compare with the available literature and with our historical data on relapsed/refractory ALL. Secondary objectives are:

To determine the safety and feasibility of a bortezomib-based regimen for salvage relapsed/refractory ALL in our setting.
To determine the rate of patients who are able to proceed with HSCT after the treatment.
To calculate event-free survival and overall survival after the salvage regimen for relapsed/refractory ALL.
To calculate the rate of measurable residual disease (MRD) negative status after the treatment.
To examine the rate of febrile neutropenia, liver toxicity, neurotoxicity, and treatment-related mortality after this regimen in relapsed/refractory ALL.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

50 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Bortezomib-based Regimen for Refractory or Relapsed Acute Lymphoblastic Leukemia in Adults

Anticipated Study Start Date :

Sep 1, 2023

Anticipated Primary Completion Date :

Aug 1, 2028

Anticipated Study Completion Date :

Aug 1, 2029

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Bortezomib Patients with refractory or relapsed acute lymphoblastic leukemia will receive one-two courses of salvage regimen composed by: Bortezomib 1.3 mg/m2 I.V. D1,D4,D8,D11; Vincristine 1.5 mg/m2 I.V. (maximum at 2 mg) - D1, D8,D15,D22; Doxorubicin 60 mg/m2 I.V. - D1; Peg-asparaginase 2000 IU/m2 I.V. - D4 and D18; Dexamethasone 20 mg/m2 P.O. or I.V. (divided BID) - D1-D5 and D15-D19 Intrathecal chemotherapy: methotrexate 12 mg + dexamethasone 2 mg.	Drug: Bortezomib Patients should receive one or two courses of this regimen, aiming to achieve complete remission as a bridge to proceed with allogeneic HSCT. Other Names: Vincristine Doxorubicin Peg-asparaginase Dexamethasone Methotrexate

Arm

Intervention/Treatment

Experimental: Bortezomib

Patients with refractory or relapsed acute lymphoblastic leukemia will receive one-two courses of salvage regimen composed by: Bortezomib 1.3 mg/m2 I.V. D1,D4,D8,D11; Vincristine 1.5 mg/m2 I.V. (maximum at 2 mg) - D1, D8,D15,D22; Doxorubicin 60 mg/m2 I.V. - D1; Peg-asparaginase 2000 IU/m2 I.V. - D4 and D18; Dexamethasone 20 mg/m2 P.O. or I.V. (divided BID) - D1-D5 and D15-D19 Intrathecal chemotherapy: methotrexate 12 mg + dexamethasone 2 mg.

Drug: Bortezomib

Patients should receive one or two courses of this regimen, aiming to achieve complete remission as a bridge to proceed with allogeneic HSCT.

Other Names:

Vincristine

Doxorubicin

Peg-asparaginase

Dexamethasone

Methotrexate

Outcome Measures

Primary Outcome Measures

Complete response [30 days]
Disappearance of lymphoid blasts in peripheral blood, with fewer than 5% of lymphoid blasts quantified in the bone marrow aspirate through immunophenotyping.

Secondary Outcome Measures

Event-free survival [1 year]
Time interval between study enrollment and the occurrence of an event (non-response, relapse, or death) or last follow-up (censorship).
Overall survival [1 year]
Time interval between study enrollment and the occurrence of death or last follow-up (censorship).
Rate of MRD-negativity [60 days]
Absence of pathological lymphoid blasts in a bone marrow sample detected through immunophenotyping with a minimum sensitivity of 10-4.
Rate of allogeneic hematopoietic stem-cell transplantation [1 year]
Proportion of patients who successfully underwent allogeneic hematopoietic stem-cell transplantation after the study therapy

Eligibility Criteria

Criteria

Ages Eligible for Study:

16 Years to 60 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients between 16 and 60 years-old with refractory or relapsed ALL (≥1% of anomalous blasts by flow cytometry in bone marrow or peripheral blood) after one or two lines of therapy, regardless of their phenotype or baseline genetic alteration;
Patients are eligible after allogeneic HSCT as long as patients are not actively being treated for graft-versus-host-disease (GvHD).