Clinical trial · Interventional
Allogeneic Stem Cell Transplantation vs. Conventional Therapy as Salvage Therapy for Relapsed / Progressive Patients With Multiple Myeloma After First-line Therapy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The reason for the end of recruitment is that the recruitment target could not be achieved despite all efforts and the G-BA (financing party) does not consider a continuation of the AlloRelapseMM study to be expedient.
Summary
Brief summary (as posted)
Allogeneic stem cell (allo SCT) transplantation for multiple myeloma is a potential curative treatment, but is associated with morbidity and treatment related mortality. Approved drug combinations or another autologous stem cell transplantation (auto-SCT) can be used for relapsed patients resulting in a median progression free survival up to 2-3 years. In the current trial after first-line treatment relapsed or progressed myeloma patients with an HLA compatible donor will be randomized after 3 cycles of salvage therapy to allogeneic stem cell transplantation or to continuous conventional salvage therapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (12)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Allogeneic Stem Cells | Drug | — | UNRESOLVED |
| Autologous Stem Cells | Drug | — | UNRESOLVED |
| carfilzomib/daratumumab/dexamethasone (KDD) | Drug | — | UNRESOLVED |
| carfilzomib/lenalidomide/dexamethasone (KRD) | Drug | — | UNRESOLVED |
| daratumumab/bortezomib/dexamethasone (DVD) | Drug | — | UNRESOLVED |
| daratumumab/lenalidomide/dexamethasone (DRD) | Drug | — | UNRESOLVED |
| daratumumab/pomalidomide/dexamethasone (DPD) | Drug | — | UNRESOLVED |
| elotuzumab/lenalidomide/dexamethasone (ERD) | Drug |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Arm A (allo SCT)
- description
- Allogeneic stem cell transplantation
- interventionNames
- Drug: Allogeneic Stem Cells
- type
- ACTIVE_COMPARATOR
- label
- Arm B (conventional therapy)
- description
- Currently approved triple regimens for first relapse: * carfilzomib/lenalidomide/dexamethasone (KRD) or * elotuzumab/lenalidomide/dexamethasone (ERD) or * daratumumab/bortezomib/dexamethasone DVD) or * daratumumab/lenalidomide/dexamethasone (DRD) or * ixazomib/lenalidomide/dexamethasone (IRD) or * pomalidomide/bortezomib/dexamethasone (PVD) or * carfilzomib/daratumumab/dexamethasone (KDD) or * daratumumab/pomalidomide/dexamethasone (DPD) or * isatuximab/carfilzomib/dexamethasone (Isa-KD) or * selinexor/bortezomib/dexamethasone (SVD) Alternatively, autologous stem cell transplantation may also be performed, if sufficient stem cells are still cryopreserved.
- interventionNames
- Drug: carfilzomib/lenalidomide/dexamethasone (KRD)
- Drug: elotuzumab/lenalidomide/dexamethasone (ERD)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: Patients eligible for study inclusion must meet criteria 1- 7 at registration and all of the following criteria before randomization: 1. Multiple Myeloma 2. Age 18 - 65 years 3. A signed informed consent form must be obtained before participation in the study 4. Age 66 - 70 years, if comorbidity index according to Sorror score = 0 and ECOG ≤ 1 5. 1st relapse/ progression according to IMWG criteria after first-line therapy (consisting of induction therapy followed by autologous transplantation once or twice and maintenance therapy), Additionally: meeting the need for treatment based on the SLiM-CRAB-criteria 6. Negative pregnancy test in female patients 7. Maximum of 1 cycle salvage therapy prior to study inclusion 8. Availability of a fully compatible stem cell donor (HLA-ident. Sibling or 10/10 MUD or 9/10 MMUD if mismatch affects DQB) after 3 cycles salvage therapy 9. CR/PR or SD according to IMWG-criteria after 3 cycles salvage therapy within the study Exclusion Criteria: Patients are excluded from the study if any one of criteria 1-6 are met at registration and if criterion 7 is met before randomization: 1. Non-sufficient organ function defined as: Bilirubin (in the absence of Meulengracht's disease), SGPT or SGOT ≥3 higher than normal values Cardiac ejection fraction ≤ 50% GFR \< 30 ml/min DLCO \< 35 % or continuous oxygen dependency 2. Active hepatitis B or C infection or uncontrolled HIV infection 3. Other, active malignant disease 4. Prior treatment with allogeneic stem cells 5. Participation in a clinical trial or taking an IMP within 30 days or five times the half-life of the IMP, whichever is longer, prior to registration 6. Positive serum pregnancy test at screening and before first treatment or breastfeeding 7. PD under salvage therapy
References
Publications (1)
- DERIVEDGlockner A, Schonland S, Einsele H, Kroger N. Rationale and design of the multicenter, national, randomized, open labeled phase III trial: allogeneic stem cell transplantation as a potential curative treatment for patients with relapsed or progressed multiple myeloma (AlloRelapseMM Study). BMC Cancer. 2025 Jan 27;25(1):147. doi: 10.1186/s12885-025-13503-7. PMID 39865222