POEMS Syndrome Treatment With Lenalidomide

POEMS Syndrome Clinical Trial

— POEMS  

Official title:

Phase II Trial With Lenalidomide-Dexamethasone Combination in the Treatment of POEMS Syndrome.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01639898
• Other study ID #: I10 015
• Status: Completed
• Phase: Phase 2
• Start date: July 2012
• Est. completion date: July 2018

Study information

• Verified date: July 2019
• Source: University Hospital, Limoges
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

POEMS syndrome is a rare form of B cell dyscrasia combining a proliferation usually of plasma cells, a polyneuropathy, osteocondensing bone lesions and multiple other clinical signs. Lenalidomide appears to be particularly efficient in this pathology.

The investigators propose a phase II multicentre protocol, based on the use of lenalidomide combined with dexamethasone in patients presenting a POEMS syndrome, either de novo or resistant or in relapse.

Patients who can be treated by local radiation or intensive treatment with stem cell support will undergo 2 cycles of the lenalidomide-dexamethasone (Len-Dex) combination before radiation or intensive treatment (Group 1), the other patients will undergo 9 cycles of the Len-Dex combination (Group 2).

A biological study is coupled with this clinical protocol in order to define the best biological markers predicting clinical responses, to better understand the POEMS pathophysiological mechanisms and to set up a bank of samples which can be used to study this rare pathology.

Description:

The investigators propose to simultaneously set up two Phase II therapeutic trials: Trial "2 cycles" and trial "9 cycles" (Fleming plan in one stage).

This will mean prospective multicentre studies, around a treatment with the lenalidomide-dexamethasone combination in patients suffering from POEMS syndrome either de novo, resistant or in relapse.

Both trials carried out in parallel are complementary regarding the eligibility criteria:

• Group 1: the "2-cycles" trial will be available to patients who can be treated by radiation or intensive treatment (75 % of cases occurring in front line); they will then undergo 2 cycles of the lenalidomide-dexamethasone combination before radiation or intensive treatment (Group 1).

• Group 2 : the "9-cycles" trial will be available to all other front-line patients (25 % of front-line patients) or patients in relapse or resistant, they will undergo 9 cycles of the lenalidomide-dexamethasone combination followed by maintenance therapy with lenalidomide alone for one year (Group 2).

Both these trials carried out within the same study will enable us to answer the question of potential efficacy of lenalidomide in POEMS syndrome and could enable us to draw up a new therapeutic standard.

Main objective:

Group 1: to evaluate the efficacy of the Len-Dex combination on the biological response after 2 cycles in patients with POEMS syndrome who can undergo radiation or intensive treatment.

Group 2: to evaluate the efficacy of the Len-Dex combination on the biological response in patients with POEMS syndrome who cannot be treated by radiation or intensive treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 51
• Est. completion date: July 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients suffering from POEMS syndrome (Mayo Clinic criteria)

• Patients with a localised disease who can be treated with radiation and those with a disseminated disease and who can be treated intensively will be included in Group 1, all other patients will be included in Group 2.

• Patients aged of 18 or more

• Patients who do not show uncontrolled thrombosis

• Patients who have been duly informed and who have signed a consent form.

• Patients must respect all the lenalidomide Pregnancy Prevention Program (PPP) requirements described in appendix of the protocol.

• Patients registered with the French National Health System.

Exclusion Criteria:

• Women who are pregnant, or suspected to be pregnant or breastfeeding

• Pathology not linked with POEMS, contraindicating one of the studied drugs

• Patients suffering from a deficiency which does not allow them full understanding of the trial requirements and which could compromise proper consent from the patient and/or observance of the protocol and continuous participation in the trial.

• Prior history of malignancy other than POEMS syndrome or active other cancer or other serious illness.

• Any contraindication to Revlimid® or to one of its excipient.

• Patient with clearance creatinine < 30mL/min.

• Hepatic insufficiency

• Patient with Absolute Neutrophil count (ANC) < 1,0 x 109/L

• Patient with platelet count < 75 x 109/L

• Use of any other experimental drug or therapy within 28 days of baseline

• Known hypersensitivity to thalidomide

• Instable, clinically significant ECG findings

• Known positive for HIV, or active infectious hepatitis, type A, B or C

• Patients under protection of a legal order.

Related Conditions & MeSH terms

• POEMS Syndrome
• Syndrome

Intervention

Drug:
• Lenalidomide and dexamethasone
2 cycles of the lenalidomide-dexamethasone (Len-Dex) combination before radiation or intensive treatment
• Lenalidomide and dexamethasone
9 cycles of the Len-Dex combination

Locations

Country	Name	City	State
France	CHU d'Angers	Angers
France	CHU de Caen	Caen
France	CHU de Lille	Lille
France	CHU de Limoges	Limoges
France	Centre Léon Bérard	Lyon
France	Hospices Civil de Lyon	Lyon
France	CHU de Nantes	Nantes
France	Hôpital Necker	Paris
France	Hôpital Saint-Louis	Paris
France	Pitié Salpétrière	Paris
France	CHU de Toulouse	Toulouse

Sponsors (3)

Lead Sponsor	Collaborator
University Hospital, Limoges	Celgene Corporation, Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Biological outcome	Decrease of monoclonal protein and serum VEGF level	Two months for group 1
Primary	Biological outcome	Decrease of monoclonal protein and serum VEGF level	2, 4 or 6 month for group 2
Secondary	Clinical response	Evaluation of the neurological (Overall Neuropathy Limitations Scale, Neuropsychological Impairment Scale and 10 m walking test) and other damages responses:	2 months