Multiple Myeloma in Relapse
Conditions
Keywords
Multiple Myeloma, Relapse, Complete Remission, Very Good Partial Remission
Brief summary
In Multiple Myeloma, an adult hematological malignancy, mainly located in the Bone Marrow (BM), dramatic recent progresses have been observed, thanks to new agents (proteasome inhibitors and IMIDs). However, at time of first relapse, high-dose therapy followed by Stem Cell Rescue (SCR) is frequently mandatory as a consolidation in minimal residual disease, to healthy patients under 65 yo, combining Melphalan (MPH) and/or Total Body Irradiation. Modern irradiation modalities are now available by the use of HI-ART Tomotherapy system to realize a Total Bone Marrow Irradiation (TBMI), in order both to limit the dose administered to Organ at Risk (lungs, oral cavity) and to focus efficacy on BM. In this phase-1 study, the conditioning regimen before SCR will combine a fixed high-dose MPH (140 mg/m²) and a dose escalated TBMI, so as to define its Maximal Tolerated Dose (MTD) and the Dose Limiting Toxicities (DLT). An extended cohort will further in a phase-2 setting.
Detailed description
Experimental : Total Bone Marrow Irradiation (TBMI) is delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3. The escalated dose levels are determined according to a 3x3 modified Fibonacci method and five dose levels will be explored. The doses per fraction are: 1gy, 1.25gy, 1.5gy, 1.75gy and 2gy, and consequently the cumulative TBMI doses are: 8gy, 10gy, 12gy, 14gy and 16gy. Drug : Melphalan is infused intravenously in 30 minutes on day -2 after IV anti-emetics. Autologous Peripheral Stem Cell Rescue : are re-infused in the central line on day 0 after adequate premedication. Despite the recent finding of new drugs (proteasome inhibitors and IMIDs), Multiple Myeloma still remain uncurable, especially after the first relapse, even in responding disease under conventional chemotherapy. In the healthy youngest patients (\<65 yo), when peripheral stem cells collection is available, a high-dose therapy is often proposed in consolidation of complete or very good partial remission: the conditioning regimen usually includes high dose alkylating agent (mostly Melphalan) and/or Total Body Irradiation. The new Tomotherapy HI-ART technology allows irradiating on a 1.6m length field all the bone marrow sites together with optimal respect of the Organ at Risk (lungs, oral cavity, heart, liver, kidneys…). The proposed phase-1 study will explore the safety and efficacy of escalated dose of Total Bone-Marrow Irradiation in combination with a fixed dose of Melphalan (140mg/m²), followed by autologous SCR. To determine the MTD is the main objective of the study, then the toxicity profile (DLTs) and the RP2D in an extended cohort at the MTD dose.
Interventions
Total Bone Marrow Irradiation (TBMI): 8 Gy
Total Bone Marrow Irradiation (TBMI): 10 Gy
Total Bone Marrow Irradiation (TBMI): 12 Gy
Total Bone Marrow Irradiation (TBMI): 14 Gy
Total Bone Marrow Irradiation (TBMI): 16 Gy
Sponsors
Study design
Intervention model description
Total Bone Marrow Irradiation (TBMI) dose escalation
Eligibility
Inclusion criteria
* Multiple Myeloma in first relapse. * In Complete or very good partial remission * Available Collected Autologous Peripheral Stem cells: 2.5x106 CD34+/Kg
Exclusion criteria
* Uncontrolled visceral disease: kidney, heart, lung, diabetes mellitus * Previous Total body irradiation * Any previous radiation dose to the spinal cord which could reach to 45gy equivalent, including the proposed TBMI * Amyloidosis * Brain localizations
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Maximal Tolerated Dose, Type of DLTs | 1 year | Maximal Tolerated Dose Type of Dose-limiting Toxicities The escalated dose levels are determined according to a 3x3 modified Fibonacci method and five dose levels will be explored. The doses per fraction are: 1gy, 1.25gy, 1.5gy, 1.75gy and 2gy, and consequently the cumulative TBMI doses are: 8gy, 10gy, 12gy, 14gy and 16gy. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Safety Profile Recommended Dose for Phase-2 (RDP2) | 1 year | Safety profile: acute, short and middle term toxicities Recommended Dose for Phase-2 (RDP2) and Extended Cohort for 14 patients at this dose |
Other
| Measure | Time frame | Description |
|---|---|---|
| Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | 1 and 2 years | osteo-medullary PET fixations evaluation by FDG PET-Scan Disease-free survival at 1 year and Overall Survival |
Countries
France
Participant flow
Recruitment details
Study start date: April 9, 2013 Study completion date: October 6, 2020
Participants by arm
| Arm | Count |
|---|---|
| Total Bone Marrow Irradiation (TBMI): 8 Gy Cohort 1: Total Bone Marrow Irradiation (TBMI): 8 Gy delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3.
Melphalan 140 mg/m² infused intravenously during 30 minutes on day -2 after IV anti-emetics.
Autologous Peripheral Stem Cell Rescue : re-infused in the central line on day 0 after adequate premedication. | 3 |
| Total Bone Marrow Irradiation (TBMI): 10 Gy Cohort 2: Total Bone Marrow Irradiation (TBMI): 10 Gy delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3.
Melphalan 140 mg/m² infused intravenously during 30 minutes on day -2 after IV anti-emetics.
Autologous Peripheral Stem Cell Rescue : re-infused in the central line on day 0 after adequate premedication. | 3 |
| Total Bone Marrow Irradiation (TBMI): 12 Gy Cohort 3: Total Bone Marrow Irradiation (TBMI): 12 Gy delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3.
Melphalan 140 mg/m² infused intravenously during 30 minutes on day -2 after IV anti-emetics.
Autologous Peripheral Stem Cell Rescue : re-infused in the central line on day 0 after adequate premedication. | 6 |
| Total Bone Marrow Irradiation (TBMI): 14 Gy Cohort 4: Total Bone Marrow Irradiation (TBMI): 14 Gy delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3.
Melphalan 140 mg/m² infused intravenously during 30 minutes on day -2 after IV anti-emetics.
Autologous Peripheral Stem Cell Rescue : re-infused in the central line on day 0 after adequate premedication. | 1 |
| Total Bone Marrow Irradiation (TBMI): 16 Gy Cohort 5: Total Bone Marrow Irradiation (TBMI): 16 Gy delivered by the Tomotherapy HI-ART machine, in 2 fractions per day during 4 consecutive days from d -6 to d -3.
Melphalan 140 mg/m² infused intravenously during 30 minutes on day -2 after IV anti-emetics.
Autologous Peripheral Stem Cell Rescue : re-infused in the central line on day 0 after adequate premedication. | 0 |
| Total | 13 |
Baseline characteristics
| Characteristic | Total | Total Bone Marrow Irradiation (TBMI): 10 Gy | Total Bone Marrow Irradiation (TBMI): 12 Gy | Total Bone Marrow Irradiation (TBMI): 14 Gy | Total Bone Marrow Irradiation (TBMI): 8 Gy | Total Bone Marrow Irradiation (TBMI): 16 Gy |
|---|---|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 13 Participants | 3 Participants | 6 Participants | 1 Participants | 3 Participants | 0 Participants |
| Race and Ethnicity Not Collected | 0 Participants | — | — | — | — | — |
| Region of Enrollment France | 13 Participants | 3 Participants | 6 Participants | 1 Participants | 3 Participants | — |
| Sex: Female, Male Female | 5 Participants | 2 Participants | 2 Participants | 1 Participants | 0 Participants | 0 Participants |
| Sex: Female, Male Male | 8 Participants | 1 Participants | 4 Participants | 0 Participants | 3 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk | EG004 affected / at risk |
|---|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 3 | 0 / 3 | 0 / 6 | 0 / 1 | 0 / 0 |
| other Total, other adverse events | 3 / 3 | 3 / 3 | 6 / 6 | 1 / 1 | 0 / 0 |
| serious Total, serious adverse events | 1 / 3 | 1 / 3 | 2 / 6 | 0 / 1 | 0 / 0 |
Outcome results
Maximal Tolerated Dose, Type of DLTs
Maximal Tolerated Dose Type of Dose-limiting Toxicities The escalated dose levels are determined according to a 3x3 modified Fibonacci method and five dose levels will be explored. The doses per fraction are: 1gy, 1.25gy, 1.5gy, 1.75gy and 2gy, and consequently the cumulative TBMI doses are: 8gy, 10gy, 12gy, 14gy and 16gy.
Time frame: 1 year
Population: The study was terminated prematurely, due to a lack of enrolments
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Maximal Tolerated Dose, Type of DLTs | DLT: Severe sepsis | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Maximal Tolerated Dose, Type of DLTs | Patients without DLT | 3 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Maximal Tolerated Dose, Type of DLTs | Patients without DLT | 3 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Maximal Tolerated Dose, Type of DLTs | DLT: Severe sepsis | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Maximal Tolerated Dose, Type of DLTs | DLT: Severe sepsis | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Maximal Tolerated Dose, Type of DLTs | Patients without DLT | 5 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Maximal Tolerated Dose, Type of DLTs | DLT: Severe sepsis | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Maximal Tolerated Dose, Type of DLTs | Patients without DLT | 1 Participants |
Safety Profile Recommended Dose for Phase-2 (RDP2)
Safety profile: acute, short and middle term toxicities Recommended Dose for Phase-2 (RDP2) and Extended Cohort for 14 patients at this dose
Time frame: 1 year
Population: The study was terminated prematurely, due to a lack of enrolments. The recommended dose for phase-2 has not been reached. No extended cohort has been performed
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Extended Cohort performed | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Patients treated at lower dose levels | 3 Participants |
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Recommended dose reached | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Patients treated at lower dose levels | 3 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Recommended dose reached | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Extended Cohort performed | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Recommended dose reached | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Patients treated at lower dose levels | 6 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Extended Cohort performed | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Recommended dose reached | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Extended Cohort performed | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Patients treated at lower dose levels | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 16 Gy | Safety Profile Recommended Dose for Phase-2 (RDP2) | Recommended dose reached | 0 Participants |
Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response
osteo-medullary PET fixations evaluation by FDG PET-Scan Disease-free survival at 1 year and Overall Survival
Time frame: 1 and 2 years
Population: The study was terminated prematurely, due to a lack of enrolments
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with very good partial response | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with complete response | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 8 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with partial response | 2 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with very good partial response | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with complete response | 2 Participants |
| Total Bone Marrow Irradiation (TBMI): 10 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with partial response | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with partial response | 2 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with very good partial response | 3 Participants |
| Total Bone Marrow Irradiation (TBMI): 12 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with complete response | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with very good partial response | 0 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with complete response | 1 Participants |
| Total Bone Marrow Irradiation (TBMI): 14 Gy | Efficacy Expressed as the Rate (%) of Complete Response and Very Good Partial Response | Patients with partial response | 0 Participants |