Phase 1 Study of Bortezomib, Fludarabine, and Melphalan, With or Without Total Marrow Irradiation, as Allogeneic Hematopoietic Stem Cell Transplant Conditioning for High-risk or Relapsed/Refractory Multiple Myeloma

Author:

Ladbury Colton1,Sanchez James2,Chowdhury Arnab3,Palmer Joycelynne3,Liu An1,Stein Anthony2,Htut Myo2,Farol Leonardo24,Cai Ji-Lian24,Somlo George2,Rosenzweig Michael2,Wong Jeffrey C.1,Sahebi Firoozeh24

Affiliation:

1. Department of Radiation Oncology, City of Hope National Medical Center, Duarte

2. Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte

3. Division of Biostatistics, Department of Computational and Quantitative Medicine, City of Hope National Medical Center, Duarte

4. Department of Hematology and Hematopoietic Cell Transplantation, Southern California Kaiser Permanente Medical Group, Los Angeles, CA

Abstract

Objectives: We conducted a phase 1 study of a conditioning regimen with or without total marrow irradiation (TMI) before allogeneic hematopoietic stem cell transplantation for patients with high-risk or refractory multiple myeloma. Methods: Eighteen patients were enrolled on one of 2 strata. Patients with no prior radiation received TMI (900 cGy), fludarabine (FLU), and melphalan (MEL) conditioning, with bortezomib added in the second cohort (stratum I). Patients with prior radiation received FLU, MEL, and bortezomib, without TMI (stratum II). Results: Eight patients were enrolled in the TMI arm (stratum I). One of 3 patients in cohort 1 experienced dose-limiting toxicity (DLT), which led to the expansion to 3 more patients with no DLT. Cohort 2 enrolled only 2 patients due to low accrual, with bortezomib, added at 0.5 mg/m2; neither experienced DLT. Nine patients were enrolled in the non-TMI arm (stratum II). Three patients were enrolled in cohort 1 (bortezomib 0.5 mg/m2) and none experienced DLT. Three were enrolled in cohort 2 (bortezomib 0.7 mg/m2), and 1 experienced DLT; therefore, the cohort expanded to 3 more patients. One more patient experienced DLT. Median overall survival on strata I and II was 44.5 months (95% CI: 1.73-not reached) and 21.6 months (95% CI: 4.1-72.7), respectively. Median progression-free survival on strata I and II was 18.1 months (95% CI: 1.73-not reached) and 8.9 months (95% CI: 2.7-24.4), respectively. Conclusion(s): TMI 900 cGy, FLU, and MEL are considered feasible as conditioning for allogeneic stem cell transplantation and may warrant further investigation due to favorable response rates and survival.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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