Alternate Day Dosing of Pomalidomide in Patients With Refractory Multiple Myeloma

Refractory Multiple Myeloma Clinical Trial

— OptiPOM  

Official title:

Alternate Day Dosing of Pomalidomide in Patients With Refractory Multiple Myeloma. A Multi-center, Single Arm Phase II Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03520985
• Other study ID #: SAKK 39/16 - OptiPOM
• Status: Terminated
• Phase: Phase 2
• Start date: October 1, 2018
• Est. completion date: February 3, 2021

Study information

• Verified date: June 2021
• Source: Swiss Group for Clinical Cancer Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 34
• Est. completion date: February 3, 2021
• Est. primary completion date: February 3, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Key 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

Key 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

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell
• Refractory Multiple Myeloma

Intervention

Drug:
• 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.
• 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.

Locations

Country	Name	City	State
Switzerland	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	St. Gallen
Switzerland	Regionalspital Thun	Thun
Switzerland	Kantonsspital Winterthur	Winterthur
Switzerland	Onkozentrum Hirslanden Zürich	Zurich
Switzerland	OnkoZentrum Zürich AG - Klinik im Park	Zürich
Switzerland	Universitätsspital Zürich	Zürich

Sponsors (1)

Lead Sponsor	Collaborator
Swiss Group for Clinical Cancer Research

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Response Rate (ORR)	OR is defined as minimal response or better, assessed according to the IMWG criteria.	From date of registration until 28 days after last dose of trial medication with longest treatment time of approximately 36 months
Secondary	Overall Survival (OS)	OS is defined as the time from registration until death from any cause. Patients not having an event at the time of analysis will be censored at the date they were last known to be alive.	From date of registration until 28 days after last dose of trial medication with longest treatment time of approximately 36 months
Secondary	Overall Survival (OS) at 12 months	OS, as defined above, will be evaluated at 12 months.	at 12 months
Secondary	Progression-free survival (PFS)	PFS is defined as the time from registration until progression according the IMWG criteria or death from any cause, whichever occurs first. Patients not having an event at the time of analysis as well as patients starting a new anticancer therapy in the absence of an event will be censored at the date of their last tumor assessment showing non-progression before starting a new treatment, if any.	From date of registration until 28 days after last dose of trial medication with longest treatment time of approximately 36 months