High Dose Therapy Followed by Autologous Transplantation for Myeloma Patients With Severe Renal Impairment
- Conditions
- Multiple MyelomaRenal Failure
- Interventions
- Other: Data collection
- Registration Number
- NCT03234335
- Brief Summary
Multiple myeloma (MM) is a malignant plasma cell disorder, characterized by the presence of more than 10 % of clonal plasma cells in the bone marrow. Therapeutic intervention is recommended when at least one of the myeloma defining events occurs (CRAB features). Renal impairment (RI) is one of the most common complications of MM, accounting for 20-30 % of MM patients at diagnosis and 40-50% of patients during the course of their disease. To date, there is no defined consensus for the management of myeloma patients with renal failure. It is then of clinical importance to better considering available therapeutic options to improve responses and survival of these patients.
- Detailed Description
RI is associated with poor prognosis and short median survival (32 months vs 55 months for MM patients with normal renal function). Thus, RI remains a major challenge for hematologists, including decisions on optimal anti-myeloma therapy, potential dialysis, supportive care and quality of life. The combination of a proteasome inhibitor and an immunomodulator is the preferred induction treatment for newly diagnosed transplant-eligible MM patients. After induction, high-dose therapy with Autologous Stem Cell Transplant (ASCT) is the standard of care for these patients. However, concerns related to management of comorbidities and treatment side effects question about therapeutic options for patients with severe renal damage. Of interest, recent studies argued that high-dose therapy followed by ASCT could be a feasible and safe method for renal failure MM patients. Yet, these observations on small sample size patients groups need to be confirmed with standardized conditions. This study proposes to evaluate the efficacy and the safety of this therapeutic strategy in MM patients with severe renal impairment.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 50
- Age ≤ 66 years-old
- Patients with symptomatic, measurable and newly diagnosed multiple myeloma associated:
- Severe renal failure at the time of transplantation (creatinine clearance < 40 ml/min/1.73m², CKD-EPI: Chronic Kidney Disease Epidemiology Collaboration)
- Partial response after induction treatment
- For patients who undergo autologous transplantation, absence of known contraindication for transplantation
- Absence of amylose
- Patient affiliated to a social security regimen or beneficiary of the same
- Signed written informed consent form
- Patient without at least a partial hematological response following the induction stage
- Medical history of previous malignancy
- Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent (art. L.1121-6, L.112-7, L.1211-8, L.1211-9)
- Pregnant or breastfeeding woman
- Declining participation
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Myeloma patients with severe renal impairment Data collection Myeloma patients with severe renal impairment. Data collection will concern myeloma patients with severe renal impairment who are susceptible to undergo autologous transplantation.
- Primary Outcome Measures
Name Time Method Non Relapse Mortality post-transplantation 100 days post-transplantation Non-relapse mortality at Day +100 post-transplantation will be reported.
- Secondary Outcome Measures
Name Time Method progression-free survival 2 years post-transplantation progression-free survival at 2 years post-transplantation will be reported.
Number of toxicities 2 years post-transplantation Number of hematological and extra-hematological toxicities linked to autologous stem cell transplantation will be reported during 2 years.
Overall survival 2 years post-transplantation Overall survival at 2 years post-transplantation will be reported.
presence of hematological response 6 months The presence of hematological response at Day+100 and at 6 months post-transplantation will be reported.
Level of renal response 3 months, 6 months and one year Level of renal response at 3 months, 6 months and one year post-transplantation will be quantified and reported.
Trial Locations
- Locations (33)
Centre Hospitalier Universitaire d'Angers
🇫🇷Angers, France
EHU Oran
🇩🇿Oran, Algeria
Centre Hospitalier de Boulogne
🇫🇷Boulogne, France
CHU Sart Tilman
🇧🇪Liège, Belgium
Centre Pierre et Marie Curie
🇩🇿Alger, Algeria
CHU de Rennes
🇫🇷Rennes, France
Hôpital Saint-Eloi
🇫🇷Montpellier, France
Centre Hospitalier Universitaire de Nancy
🇫🇷Nancy, France
Centre Hospitalier Universitaire d'Amiens
🇫🇷Amiens, France
Centre Hospitalier Universitaire de Besançon
🇫🇷Besançon, France
Centre Hospitalier de la Côte Basque
🇫🇷Bayonne, France
Centre Hospitalier d'Argenteuil
🇫🇷Argenteuil, France
CHU de Brest
🇫🇷Brest, France
Centre Hospitalier Universitaire de Caen
🇫🇷Caen, France
Centre Hospitalier Universitaire de Clermont Ferrand
🇫🇷Clermont-Ferrand, France
Centre Hospitalier de Cholet
🇫🇷Cholet, France
Centre Hospitalier Universitaire de Grenoble
🇫🇷Grenoble, France
Centre Hospitalier Universitaire de Dijon
🇫🇷Dijon, France
CHU de Limoges
🇫🇷Limoges, France
Centre Léon Bérard
🇫🇷Lyon, France
Hôpital Archet
🇫🇷Nice, France
Institut Curie
🇫🇷Paris, France
Hôpital Saint-Antoine
🇫🇷Paris, France
Groupe Hospitalier Pitié-Salpétrière
🇫🇷Paris, France
Hôpital Tenon
🇫🇷Paris, France
Hôpital Cochin
🇫🇷Paris, France
Centre Hospitalier Lyon Sud
🇫🇷Pierre-Bénite, France
Hôpital Saint-Bernard
🇫🇷Poitiers, France
Centre Hospitalier de Saint Quentin
🇫🇷Saint-Quentin, France
Hôpital Victor Provo (Roubaix)
🇫🇷Roubaix, France
CHU de Saint-Etienne
🇫🇷Saint-Priest-en-Jarez, France
Hôpitaux Universitaires de Strasbourg
🇫🇷Strasbourg, France
American University of Beirut
🇱🇧Beyrouth, Lebanon