241 Single Institution Review of Allogeneic Bone Marrow Transplantation for Multiple Myeloma: An 18 Year Experience

Track: Contributed Abstracts
Wednesday, February 13, 2013, 6:45 PM-7:45 PM
Hall 1 (Salt Palace Convention Center)
Abdul M Adjei, MD , Medical oncology, Fox Chase Cancer center, Philadelphia, PA
Vinit Karur, MD, PhD , medical Oncology, Fox chase Cancer cencter, Philadelphia, PA
Joseph Vadakara, MD , Medical Oncology, Fox Chase cancer center, Philadelphia, PA
C J Fidler , Medical Oncology, Abington Cancer Care Specialists, Abington, PA
Neel Gandhi, MD , Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA
Manish Sharma, MD , Bone Marrow Transplantation, Temple University, Philadelphia, PA
Thomas Klumpp, MD , Temple University Bone Marrow Transplant Program, Philadelphia, PA
Omotayo Fasan, MD , Hematology, Temple university Bone Marrow transplant program, Philadelphia, PA
Mary Ellen Martin, MD , Bone Marrow Transplant, Temple University, Philadelphia, PA
Patricia Lamont Kropf, MD , Temple Fox Chase Bone Marrow Trans, Philadelphia, PA
Kenneth F. Mangan, MD , Medicine, Temple University BMT Program, Philadelphia, PA

Background:

Allogeneic bone marrow transplantation (allo-BMT) in Multiple Myeloma (MM) offers a potential curative strategy. This study was undertaken to determine outcomes of patients with MM undergoing allogeneic BMT at Temple University Hospital over the past 18 years.

Methods:

We retrospectively reviewed our clinical database for patients with a diagnosis of MM who underwent an allo-BMT between 1994 to present. We reviewed the following variables: Age, sex, myeloma subtype and stage, remission status prior to transplant, stem cell source and degree of donor matching, conditioning regimen, GVHD prophylaxis. Outcome measures included overall survival, non-relapsed mortality (NRM), and acute and chronic GVHD.

Results:

Patient characteristics are summarized in the Table 1. The median age was 49.5 years, 72.7% had DSS III, 68% had either at least PR2, PD or SD/MR, and 86.3% had a MRD transplant. The outcomes are summarized in Table 2. The median actuarial overall survival for the cohort is 5.95 years and the ten year actuarial survival for the cohort is 34%. Median survival with a Calcineurin inhibitor (CUI) and methotrexate combination for GVHD prophylaxis was 14.4 years, as compared to 2.2 years for CUI and mycophenolate based regimens (p = 0.05). The relapse rate for the cohort was 31.8%, Grade 3 or more acute GVHD developed in 31.8%, while extensive chronic GVHD occurred in 30% of the patients.

Conclusion:

Allogeneic transplantation is a reasonable strategy in patients with MM which can lead to long-term survival. Patients receiving GVHD prophylaxis with a CUI and Methotrexate experienced superior survival compared to those receiving a CUI and mycophenolate based regimen.

 

Table 1: Patient Characteristics (N = 22)

 

N (%)

Median Age (years)

49.5

Sex:

Male

8 (36)

Myeloma Subtype:

Kappa light chain                  

Lambda light chain                  

IgA

IgG                         

Minimally secretory    

2 (9.1)

3 (13.6)

3 (13.6)

13 (59.1)

1 (4.5)

DSS:

I

II

III

3 (13.6)

3 (13.6)

16 (72.7)

Response prior to transplant:

CR

PR1

PR2+

SD/MR

PD

Unknown

2 (9.1)

4 (18.2)

8 (36.4)

5 (22.7)

2 (9.1)

1 (4.5)

Donor:

MUD

MRD

3 (13.6)

19 (86.3)

HLA-matching:

 9/10

10/10

10 (45.5)

12 (54.5)

Conditioning regimen:

FLU/CY                

FLU/MEL             

FLU/MEL/ATG           

MEL/TBI             

TBI                              

1 (4.5)

8 (36.4)

2 (9.1)

9 (40.9)

2 (9.1)

Source of Stem Cells:

Peripheral Blood

Bone  Marrow

8 (36.4)

14 (63.6)

GVHD prophylaxis:

CYA              

CYA/MTX          

CYA/MYC           

TAC/MTX          

TAC/MYC          

1 (4.5)

8 (36.4)

2 (9.1)

2 (.1)

9 (40.9)

 

Table 2:  Transplant Outcomes

Median OS (years)

5.9548

Acute GVHD  Grade:

 

0-2        

 

3-5  

15 (68.2)

7 (31.8)

Chronic GVHD:

None

Limited

Extensive

10 (50)

4 (20)

6 (30)

NRM at 1 year

7 (35%)

Median Survival (years)

per GVHD prophylaxis regimen:

Calcineurin inhibitor/MTX

Calcineurin inhibitor/MYC

14.4

2.3