Autologous Transplantation, Consolidation, and Maintenance Therapy in Multiple Myeloma: Results of the BMT CTN 0702 Trial

Author:

Stadtmauer Edward A.1,Pasquini Marcelo C.2,Blackwell Beth3,Hari Parameswaran2,Bashey Asad4,Devine Steven5,Efebera Yvonne5,Ganguly Siddharta6,Gasparetto Cristina7,Geller Nancy8,Horowitz Mary M.2,Koreth John9,Knust Kristin3,Landau Heather10,Brunstein Claudio11,McCarthy Philip12,Nelson Courtney3,Qazilbash Muzaffar H.13,Shah Nina14,Vesole David H.15,Vij Ravi16,Vogl Dan T.1,Giralt Sergio10,Somlo George17,Krishnan Amrita17

Affiliation:

1. University of Pennsylvania, Philadelphia, PA

2. Medical College of Wisconsin, Milwaukee, WI

3. The Emmes Corporation, Rockville, MD

4. BMT Group of Georgia, Atlanta, GA

5. The Ohio State University, Columbus, OH

6. University of Kansas Hospital, Kansas City, KS

7. Duke University, Durham, NC

8. National Heart, Lung, and Blood Institute, Rockville, MD

9. Dana-Farber Cancer Institute, Boston, MA

10. Memorial Sloan Kettering Cancer Center, New York, NY

11. University of Minnesota, Minneapolis, MN

12. Roswell Park Cancer Institute, Buffalo, NY

13. The University of Texas MD Anderson Cancer Center, Houston, TX

14. University of California, San Francisco, San Francisco, CA

15. Hackensack University, Hackensack, NJ

16. Washington University, St Louis, MO

17. City of Hope, Los Angeles, CA

Abstract

PURPOSE Single-cycle melphalan 200 mg/m2 and autologous hematopoietic cell transplantation (AHCT) followed by lenalidomide (len) maintenance have improved progression-free survival (PFS) and overall survival (OS) for transplantation-eligible patients with multiple myeloma (MM). We designed a prospective, randomized, phase III study to test additional interventions to improve PFS by comparing AHCT, tandem AHCT (AHCT/AHCT), and AHCT and four subsequent cycles of len, bortezomib, and dexamethasone (RVD; AHCT + RVD), all followed by len until disease progression. PATIENTS AND METHODS Patients with symptomatic MM within 12 months from starting therapy and without progression who were age 70 years or younger were randomly assigned to AHCT/AHCT + len (n = 247), AHCT + RVD + len (n = 254), or AHCT + len (n = 257). The primary end point was 38-month PFS. RESULTS The study population had a median age of 56 years (range, 20 to 70 years); 24% of patients had high-risk MM, 73% had a triple-drug regimen as initial therapy, and 18% were in complete response at enrollment. The 38-month PFS rate was 58.5% (95% CI, 51.7% to 64.6%) for AHCT/AHCT + len, 57.8% (95% CI, 51.4% to 63.7%) for AHCT + RVD + len, and 53.9% (95% CI, 47.4% to 60%) for AHCT + len. For AHCT/AHCT + len, AHCT + RVD + len, and AHCT + len, the OS rates were 81.8% (95% CI, 76.2% to 86.2%), 85.4% (95% CI, 80.4% to 89.3%), and 83.7% (95% CI, 78.4% to 87.8%), respectively, and the complete response rates at 1 year were 50.5% (n = 192), 58.4% (n = 209), and 47.1% (n = 208), respectively. Toxicity profiles and development of second primary malignancies were similar across treatment arms. CONCLUSION Second AHCT or RVD consolidation as post-AHCT interventions for the up-front treatment of transplantation-eligible patients with MM did not improve PFS or OS. Single AHCT and len should remain as the standard approach for this population.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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