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AUTOLOGOUS STEM CELL TRANSPLANTATION IN ELDERLY MULTIPLE MYELOMA PATIENTS
Author(s): ,
Michela Staderini
Affiliations:
Hematology Department,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Chiara Nozzoli
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Elisabetta Antonioli
Affiliations:
Hematology Department,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Irene Donnini
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Ilaria Cutini
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Agata Suellen Guarrera
Affiliations:
Hematology Department,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Massimo Di Gioia
Affiliations:
Hematology Department,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Antonella Gozzini
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Stefano Guidi
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
,
Alberto Bosi
Affiliations:
Hematology Department,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
Riccardo Saccardi
Affiliations:
BMT Unit,Azienda Ospedaliero-Universitaria Careggi,Florence,Italy
(Abstract release date: 05/18/17) EHA Library. Staderini M. 05/18/17; 182697; PB1983
Dr. Michela Staderini
Dr. Michela Staderini
Contributions
Abstract

Abstract: PB1983

Type: Publication Only

Background

Autologous stem cell transplantation (ASCT) is currently approved as a “gold standard” first line treatment for multiple myeloma (MM) patients (pts) under 65 year old but the procedure could also be considered feasible in fit elderly patients based on several retrospective studies.

Aims

The aim of our study was to retrospectively evaluate the tolerability and the efficacy of high dose chemotherapy followed by ASCT in selected ≥65 year old MM population.

Methods

We retrospectively analyzed consecutive MM pts aged 65 or older who underwent upfront ASCT at our institution from January 2009 to November 2016. Each patient received induction therapy including proteasome inhibitors and/or immunomodulatory drugs (bortezomib and/or thalidomide based), followed by high-dose cyclophosphamide plus G-CSF and subsequently underwent peripheral blood stem cells (PBSC) collection.

Results
Overall we analized 35 pts: 21 males and 14 females (median age 66, range 65-70); 23 had IgG MM, 4 had IgA MM and 8 had light chain MM. Induction therapy was bortezomib-based (bortezomib in combination with dexamethasone, VD, in 7, or VD plus thalidomide in 26 pts) for a median of 4 cycles (range 3-6), 2 patients received thalidomide plus dexamethasone (6-12 cycles). PBSC were collected after high-dose cyclophosphamide (2 g/sqm in 2 pts, 3 g/sqm in 11 pts, 4 g/sqm in 22 pts) plus G-CSF; plerixafor was administered in 4 pts. Three pts also received lenalidomide and dexamethasone to improve the depth of response before ASCT. At the time of conditioning, among 34 evaluable pts, 8/34 pts were in complete response/stringent complete response (CR/sCR), 19/34 in very good partial response (VGPR), 5/34 in partial response (PR) and 2/34 in stable disease (SD). The conditioning regimen consisted of melphalan 140 mg/sqm in 11 pts or 200 mg/sqm in 24 pts. A median number of 4.11 x10^6 CD34+ cells/Kg was reinfused (range 2.09-10.44). The most frequent complication was fever (9 pts) with gram negative bacteremia documented in 3/9 and gram positive bacteremia in 1/9. Other complications were represented by 1 case of atrial fibrillation and 3 cases of pneumonia and 1 case of VZV reactivation. All 35 pts achieved neutrophils recovery after a median of 12 days (range 8-25) and platelets recovery after a median of 13 days (range 8-45) after transplant. No grade 3-4 toxicities were recorded. No transplant-related mortality was recorded within 100 days post transplantation. Three months after ASCT, among 28 evaluable pts, 10/28 pts were in CR, 14/28 pts in VGPR and 4/28 pts in PR. Three pts underwent tandem ASCT. After a median follow-up of 32 months (range 3-96) among 33 evaluable pts, 20 experienced disease relapse and 7 deaths occurred. Median PFS and OS were 21 and 40 months.

Conclusion
Our data support the use of ASCT as an effective and safe first-line treatment approach also in elderly MM pts. A careful patient selection is needed to reduce the toxicity of the procedure.

Session topic: 14. Myeloma and other monoclonal gammopathies - Clinical

Keyword(s): Myeloma, Elderly, ABMT

Abstract: PB1983

Type: Publication Only

Background

Autologous stem cell transplantation (ASCT) is currently approved as a “gold standard” first line treatment for multiple myeloma (MM) patients (pts) under 65 year old but the procedure could also be considered feasible in fit elderly patients based on several retrospective studies.

Aims

The aim of our study was to retrospectively evaluate the tolerability and the efficacy of high dose chemotherapy followed by ASCT in selected ≥65 year old MM population.

Methods

We retrospectively analyzed consecutive MM pts aged 65 or older who underwent upfront ASCT at our institution from January 2009 to November 2016. Each patient received induction therapy including proteasome inhibitors and/or immunomodulatory drugs (bortezomib and/or thalidomide based), followed by high-dose cyclophosphamide plus G-CSF and subsequently underwent peripheral blood stem cells (PBSC) collection.

Results
Overall we analized 35 pts: 21 males and 14 females (median age 66, range 65-70); 23 had IgG MM, 4 had IgA MM and 8 had light chain MM. Induction therapy was bortezomib-based (bortezomib in combination with dexamethasone, VD, in 7, or VD plus thalidomide in 26 pts) for a median of 4 cycles (range 3-6), 2 patients received thalidomide plus dexamethasone (6-12 cycles). PBSC were collected after high-dose cyclophosphamide (2 g/sqm in 2 pts, 3 g/sqm in 11 pts, 4 g/sqm in 22 pts) plus G-CSF; plerixafor was administered in 4 pts. Three pts also received lenalidomide and dexamethasone to improve the depth of response before ASCT. At the time of conditioning, among 34 evaluable pts, 8/34 pts were in complete response/stringent complete response (CR/sCR), 19/34 in very good partial response (VGPR), 5/34 in partial response (PR) and 2/34 in stable disease (SD). The conditioning regimen consisted of melphalan 140 mg/sqm in 11 pts or 200 mg/sqm in 24 pts. A median number of 4.11 x10^6 CD34+ cells/Kg was reinfused (range 2.09-10.44). The most frequent complication was fever (9 pts) with gram negative bacteremia documented in 3/9 and gram positive bacteremia in 1/9. Other complications were represented by 1 case of atrial fibrillation and 3 cases of pneumonia and 1 case of VZV reactivation. All 35 pts achieved neutrophils recovery after a median of 12 days (range 8-25) and platelets recovery after a median of 13 days (range 8-45) after transplant. No grade 3-4 toxicities were recorded. No transplant-related mortality was recorded within 100 days post transplantation. Three months after ASCT, among 28 evaluable pts, 10/28 pts were in CR, 14/28 pts in VGPR and 4/28 pts in PR. Three pts underwent tandem ASCT. After a median follow-up of 32 months (range 3-96) among 33 evaluable pts, 20 experienced disease relapse and 7 deaths occurred. Median PFS and OS were 21 and 40 months.

Conclusion
Our data support the use of ASCT as an effective and safe first-line treatment approach also in elderly MM pts. A careful patient selection is needed to reduce the toxicity of the procedure.

Session topic: 14. Myeloma and other monoclonal gammopathies - Clinical

Keyword(s): Myeloma, Elderly, ABMT

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