Alternate Day Dosing of Pomalidomide in Patients With Refractory Multiple Myeloma

NCT ID: NCT03520985

Last Updated: 2021-06-10

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-10-01
• Study Completion Date: 2021-02-03

Brief Summary

Pomalidomide is an approved treatment for refractory multiple myeloma. Toxicity of pomalidomide in the pivotal MM-003 trial, was considerable, with 60% of patients experiencing drug-related G3/4 toxicity. Neutropenia (48% vs 16%) and pneumonia (13% vs 8%) were significantly more common in the pomalidomide arm. This resulted in frequent dose interruptions (67%) and dose reductions (27%). This suggests that for the majority of patients the 4 mg daily dosing schedule is too toxic, and that strategies to deliver reduced dosing of pomalidomide are of high practical relevance. The aim of this trial therefore is to establish that alternate day dosing of pomalidomide (4 mg q2d, d1-28) is non-inferior to daily dosing (4 mg d1-21 q28) in terms of efficacy of the drug with potentially less side effects.

Detailed Description

Multiple myeloma (MM) accounts for 1% of all cancers and ∼10% of all hematological malignancies. Despite recent advances in myeloma treatment, including the introduction of proteasome inhibitors, immunomodulatory drugs (IMiDs) and stem cell transplantation, myeloma remains an incurable disease. The treatment of bortezomib and lenalidomide refractory myeloma is still an unmet medical need. Once patients have relapsed after IMiD-containing therapies and have become bortezomib-resistant, their prognosis is extremely poor.

Pomalidomide is a third-generation, Swissmedic approved, oral immunomodulatory drug with activity in such patients. However the toxicity of pomalidomide in the pivotal MM-003 trial was considerable, with 60% of patients experiencing drug-related G3/4 toxicity. Neutropenia (48% vs 16%) and pneumonia (13% vs 8%) were significantly more common in the pomalidomide arm. This resulted in frequent dose interruptions (67%) and dose reductions (27%). This suggests that for the majority of patients the 4 mg daily dosing schedule (4 mg daily on 21 of 28 days) is toxic, and that strategies to deliver reduced dosing of pomalidomide are of high practical relevance.

Alternative dosing schedules:

There is robust data available indicating that lower pomalidomide doses (e.g. 2 mg daily) lead to similar responses and progression free survival with fewer side effects. Due to its unique pharmacological characteristics, pomalidomide is well suited for alternate day dosing. The decline of the plasma concentration at the terminal phase is slow. These data make pomalidomide an ideal candidate for alternate day dosing. Therefore, a phase I study has already been conducted in 2008 to test the alternating administration of the drug showing excellent responses with a marked reduction of thrombotic events and less severe myelosuppression.

The drug costs of pomalidomide are quite high. Interestingly, the manufacturer determined a pricing model that is independent from the capsule strength (costs for one capsule 1 mg=2 mg=3 mg=4 mg). In patients requiring dose reductions due to hematologic toxicity, daily dosing of reduced strength pomalidomide (e.g. 2 mg daily) is approved and suggested by the manufacturer. This delivers 50% less pomalidomide to the patient, albeit at 100% of the price of full dosing.

In summary, the establishment of the modified pomalidomide schedule would be an interesting option for our patients to achieve similar efficacy with fewer side effects. In addition, it would optimize the cost-effectiveness of the drug.

Conditions

Refractory Multiple Myeloma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Pomalidomide

The treatment in this trial consists of oral pomalidomide on alternate days (ad) plus Low-Dose Dexamethasone (adPOM + LD-DEX)

Group Type: EXPERIMENTAL

Pomalidomide

Intervention Type: DRUG

Pomalidomide (4 mg p.o.) will be administered on every other day of each 28-day treatment cycle.

Treatment duration:

Treatment cycles are repeated until confirmed disease progression.

Dexamethasone

Intervention Type: DRUG

For patients ≤ 75 years of age:

Low-Dose Dexamethasone (40 mg p.o.) will be administered once per day on days 1, 7, 15, and 21 of a 28-day cycle.

For patients > 75 years of age:

Low-Dose Dexamethasone (20 mg p.o.) will be administered once per day on days 1, 7, 15, and 21 of a 28-day cycle.

Treatment duration:

Treatment cycles are repeated until confirmed disease progression.

Interventions

Pomalidomide

Pomalidomide (4 mg p.o.) will be administered on every other day of each 28-day treatment cycle.

Treatment duration:

Treatment cycles are repeated until confirmed disease progression.

Intervention Type: DRUG

Dexamethasone

For patients ≤ 75 years of age:

Low-Dose Dexamethasone (40 mg p.o.) will be administered once per day on days 1, 7, 15, and 21 of a 28-day cycle.

For patients > 75 years of age:

Low-Dose Dexamethasone (20 mg p.o.) will be administered once per day on days 1, 7, 15, and 21 of a 28-day cycle.

Treatment duration:

Treatment cycles are repeated until confirmed disease progression.

Intervention Type: DRUG

Other Intervention Names

Imnovid®

Eligibility Criteria

Inclusion Criteria

• Patient was diagnosed with multiple myeloma based on standard IMWG criteria
• Prior treatment with ≥ 2 treatment lines of anti-myeloma therapy
• Patients must have been exposed to both lenalidomide and bortezomib
• Measurable disease for myeloma defined as one of the following: serum M-protein ≥ 5 g/L; urine M-protein ≥ 0.2 g/24 hours
• Refractory or relapsed and refractory disease defined as documented disease progression during or within 60 days of completing their last myeloma therapy.
• Adequate hematological and hepatic function
• A negative pregnancy test before inclusion into the trial is required for all women with child-bearing potential

Exclusion Criteria

• History of hematologic or primary solid tumor malignancy, unless in remission for at least 3 years from registration, with the exception of pT1-2 prostate cancer Gleason score ≤6, adequately treated, cervical carcinoma in situ or localized non-melanoma skin cancer.
• Polyneuropathy grade > 2
• Patients who received any of the following within the last 14 days of initiation of trial treatment:

• Plasmapheresis
• Major surgery (kyphoplasty is not considered major surgery)
• Radiation therapy
• Use of any anti-myeloma drug therapy
• Known or clinically suspected myeloma manifestations in the central nervous system
• Severe or uncontrolled cardiovascular disease

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Swiss Cancer Institute

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thilo Zander, MD

Role: STUDY_CHAIR

Luzerner Kantonsspital

Christoph Driessen, Prof

Role: STUDY_CHAIR

Cantonal Hospital of St. Gallen

Christoph Renner, Prof

Role: STUDY_CHAIR

Onkozentrum Zürich

Locations

Kantonspital Aarau

Aarau, , Switzerland

Kantonsspital Baden (Baden/Brugg)

Baden, , Switzerland

Universitätsspital Basel

Basel, , Switzerland

Istituto Oncologico Svizzera Italiana IOSI

Bellinzona, , Switzerland

Inselspital Bern

Bern, , Switzerland

Kantonsspital Graubünden

Chur, , Switzerland

Hopital Fribourgeois HFR

Fribourg, , Switzerland

Kantonsspital Liestal

Liestal, , Switzerland

Kantonsspital Luzern

Luzerne, , Switzerland

Spital Thurgau AG

Münsterlingen, , Switzerland

Kantonsspital St. Gallen

Sankt Gallen, , Switzerland

Regionalspital Thun

Thun, , Switzerland

Kantonsspital Winterthur

Winterthur, , Switzerland

Onkozentrum Hirslanden Zürich

Zurich, , Switzerland

OnkoZentrum Zürich AG - Klinik im Park

Zurich, , Switzerland

Universitätsspital Zürich

Zurich, , Switzerland

Countries

Switzerland

Other Identifiers

SAKK 39/16 - OptiPOM

Identifier Type: -

Identifier Source: org_study_id