Iberoamerican Protocol With Thalidomide in Patients With Symptomatic Newly Diagnosed Multiple Myeloma Over 65 Years

Sponsor

Grupo de Estudos Multicentricos em Onco-Hematologia (Other)

Overall Status

Unknown status

CT.gov ID

NCT01532856

Collaborator

(none)

Enrollment

Locations

Arms

Duration (Months)

21.3

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This protocol is an international, multicenter, comparative, open and randomized study designed to compare the safety and efficacy (in terms of response rate) from three induction chemotherapy schemes -Thalidomide/Cyclophosphamide/Dexamethasone versus Thalidomide/Dexamethasone versus Thalidomide/Melphalan/Prednisone. Finally, this study is also designed to compare the safety and efficacy (in terms of duration of response) of two maintenance chemotherapy regimens - Thalidomide/Prednisone versus Thalidomide. Each treatment arm will include 100 patients and assessments and scheduled visits will be conducted in three periods: Pre-treatment, treatment and monitoring. Security will be evaluated by monitoring all adverse events, physical examination, vital signs and biochemical studies. Response to treatment will be evaluated according to the EBMT21 criteria and will be assessed on day 1 of each cycle of induction, at the end of nine cycles of induction therapy and monthly during the first year of maintenance therapy and every 3 months thereafter.

Condition or Disease	Intervention/Treatment	Phase
Multiple Myeloma	Drug: Thalidomide, Cyclophosphamide, Dexamethasone Drug: Thalidomide, Dexamethasone Drug: Thalidomide, Melphalan, Prednisone	Phase 3

Study Design

Study Type:

Interventional

Actual Enrollment :

64 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Iberoamerican Phase III International Study, Open, Multicenter, Randomized, Comparative of Thalidomide / Cyclophosphamide / Dexamethasone Versus Thalidomide / Dexamethasone Versus Thalidomide / Melphalan / Prednisone as Induction Therapy Followed by Maintenance Therapy With Thalidomide + Prednisone Versus Thalidomide Alone in Patients With Symptomatic Newly Diagnosed Multiple Myeloma Over 65years.

Study Start Date :

Jan 1, 2007

Actual Primary Completion Date :

Dec 1, 2011

Anticipated Study Completion Date :

Jun 1, 2012

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Group A induction therapy Thalidomide + Cyclophosphamide + Dexamethasone	Drug: Thalidomide, Cyclophosphamide, Dexamethasone Thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle Cyclophosphamide - 50mg per day, orally, during 9 cycles of 28 days each cycle Dexamethasone - 40mg orally(two pulses the first two cycles in days 1-4 and 15-18 and then a single pulse in each other cycle) during 9 cycles of 28 days.
Active Comparator: Group B induction therapy thalidomide + dexamethasone	Drug: Thalidomide, Dexamethasone Thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle Dexamethasone - 40mg orally, in three pulses (days 1 to 4, 9 to 12 and 17 20) odd cycles and a single pulse treatment in pairs cycles, during 9 cycles of 28 days each cycle
Active Comparator: Group C induction therapy thalidomide + melphalan + prednisone	Drug: Thalidomide, Melphalan, Prednisone thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle; melphalan - 4 mg/m2, days 1-7, orally, during 9 cycles of 28 days each cycle; prednisone - 40 mg/m2, days 1-7, orally, during 9 cycles of 28 days each cycle

Arm

Intervention/Treatment

Active Comparator: Group A induction therapy

Thalidomide + Cyclophosphamide + Dexamethasone

Drug: Thalidomide, Cyclophosphamide, Dexamethasone

Thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle Cyclophosphamide - 50mg per day, orally, during 9 cycles of 28 days each cycle Dexamethasone - 40mg orally(two pulses the first two cycles in days 1-4 and 15-18 and then a single pulse in each other cycle) during 9 cycles of 28 days.

Active Comparator: Group B induction therapy

thalidomide + dexamethasone

Drug: Thalidomide, Dexamethasone

Thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle Dexamethasone - 40mg orally, in three pulses (days 1 to 4, 9 to 12 and 17 20) odd cycles and a single pulse treatment in pairs cycles, during 9 cycles of 28 days each cycle

Active Comparator: Group C induction therapy

thalidomide + melphalan + prednisone

Drug: Thalidomide, Melphalan, Prednisone

thalidomide - 200mg per day, orally, during 9 cycles of 28 days each cycle; melphalan - 4 mg/m2, days 1-7, orally, during 9 cycles of 28 days each cycle; prednisone - 40 mg/m2, days 1-7, orally, during 9 cycles of 28 days each cycle

Outcome Measures

Primary Outcome Measures

Response rate [36 months]
Response rate is evaluated between the 3 treatment arms
Duration of response [36 months]
Duration of response was defined as the time to the first evidence of laboratorisl progreesion.

Secondary Outcome Measures

overall survival [36 months]
Overall survival (OS) was defined as the interval from randomization to death or the last follow-up for surviving patients.
event-free survival [36 months]
Event-free survival was defined as the interval from randomization to any event (death or descontinuation due to protocol violation or non-acceptable toxicities)
progression free-survival [36 months]
Progression free-survival was defined as the time between randomization and any documentation of relapse, progression, or death by any cause.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

65 years old and non candidate for autologous stem cell transplant
Patient must be newly diagnosed with Multiple Myeloma according to establish criteria symptoms. Steroid pulses administration are allowed for any required emergency prior to starting induction therapy or bisphosphonates administration
Patient must have measurable disease, defined as follows: for secretory multiple myeloma, measurable disease is defined by the presence of measurable monoclonal component in serum or in urine excretion if light chain is greater than or equal to 200 mg/24 hours(Annex 5)
Measured ECOG < 2 state level.
The patient must have a life expectancy greater than 3 months.
Adequate laboratory values prior to induction treatment initiation, defined as follow:

Platelet count ≥ 50000/mm3, hemoglobin ≥ 8 g / dl and absolute neutrophil count ≥ 1000/mm3. Lower values are permitted if they are due to BM infiltration.
Corrected serum calcium ≤ 14mg/dl.
Aspartate transaminase (AST): ≤ 2.5 x normal upper limit.
Alanine transaminase (ALT):): ≤ 2.5 x normal upper limit.
Total bilirubin: ≤ 1.5 x normal upper limit.
Serum creatinine ≤ 2 mg / dl.

Men (including vasectomy done) must use barrier contraception (latex condoms) when having sex with women of potential childbearing, and for at least four weeks after thalidomide last dose.

Exclusion Criteria:

Non-secretory MM.
Previous treatment for multiple myeloma with the exception of steroid pulses for any emergency that requires treatment before beginning the induction, administration of bisphosphonates or radiation therapy.
Basal peripheral neuropathy higher than grade 2 within 14 days of inclusion.
Known thalidomide hypersensitivity.
Use of any investigational agent within 30 days prior to their inclusion.
Known human immunodeficiency virus(HIV) infection, detectable surface antigen of hepatitis B or active infection by the hepatitis C viruses
Myocardial infarction within 6 months prior to inclusion or heart functional class III or IV according to New York Heart Association (NYHA) heart failure, angina, uncontrolled ventricular arrhythmias or acute ischemia detected by electrocardiogram or conduction system abnormalities.
Participation in another clinical trial or receiving any investigational agent.

Contacts and Locations

Locations

	Site	City	State	Country
1	Universidade Federal do Rio Grande do Sul	Porto Alegre	Rio Grande do Sul	Brazil
2	Hospital Universitário Clementino Fraga Filho	Rio de Janeiro		Brazil
3	Santa Casa de Misericórdia de São Paulo	São Paulo		Brazil