Optimal infused CD34+ cell dose in multiple myeloma patients undergoing upfront autologous hematopoietic stem cell transplantation
Autologous transplantation remains the standard of care for eligible multiple myeloma (MM) patients, yet optimal CD34<sup>+</sup> cell dose remains unclear. We conducted a retrospective study on MM patients undergoing upfront transplant between 2005 and 2021 and divided them into low (≤2.5 × 10<sup>6</sup> cells/kg) and high (>2.5 × 10<sup>6</sup> cells/kg) CD34<sup>+</sup> dose groups. We included 2479 patients, 95 in the low CD34<sup>+</sup> group and 2384 in the high CD34<sup>+</sup> group. Patients in the low CD34<sup>+</sup> group were older (63.2 vs 61.1 years, p = 0.013), more often had R-ISS III (19% vs 9%, p = 0.014), received plerixafor (60% vs 35%, p < 0.001) and transplanted after 2009 (88% vs 80%, p = 0.047). Time to neutrophil and platelet recovery was longer in the low CD34<sup>+</sup> group. Median PFS and OS were lower in the low CD34<sup>+</sup> group (31.6 vs. 43.6 months, p = 0.011 and 76.4 vs. 108.2 months, p < 0.001, respectively). Evaluation of incrementally higher CD34<sup>+</sup> dose did not show significant improvement in survival at thresholds >2.5 × 10<sup>6</sup> cells/kg. Multivariable analysis affirmed that CD34<sup>+</sup> >2.5 × 10<sup>6</sup> cells/kg was associated with better PFS (HR 0.71, p = 0.008) and OS (0.59, p < 0.001). After propensity score matching, a CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg remained a predictor of better OS (0.42, p < 0.001). In conclusion, CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg was associated with improved survival, without any additional benefit at incrementally higher doses.
Authors
- Melody Becnel (ORCID: https://orcid.org/0000-0001-6295-5433)
- Sheeba K. Thomas (ORCID: https://orcid.org/0000-0001-8596-7058)
- Yosra M. Aljawai (ORCID: https://orcid.org/0000-0002-1649-7651)
- Jae‐Hyun Lee (ORCID: https://orcid.org/0000-0002-0760-0071)
- Muzaffar H. Qazilbash (ORCID: https://orcid.org/0000-0003-2876-2886)
- Jeremy Ramdial (ORCID: https://orcid.org/0000-0002-8984-3420)
- Yago L. Nieto (ORCID: https://orcid.org/0000-0001-6034-8939)
- Neeraj Y. Saini (ORCID: https://orcid.org/0000-0001-7435-0933)
- Mark R. Tanner (ORCID: https://orcid.org/0000-0002-6516-0166)
- Robert Zygmunt Orlowski (ORCID: https://orcid.org/0000-0002-5723-4129)
- Samer A. Srour (ORCID: https://orcid.org/0000-0002-6693-2025)
- Hans Chulhee Lee (ORCID: https://orcid.org/0000-0001-8545-3292)
- Guilin Tang (ORCID: https://orcid.org/0000-0002-9482-4806)
- Elizabeth J. Shpall (ORCID: https://orcid.org/0000-0003-3947-4126)
- Curtis Marcoux (ORCID: https://orcid.org/0000-0001-5834-2597)
- Krina K. Patel (ORCID: https://orcid.org/0000-0002-8894-027X)
- Babar Pal
- Qaiser Bashir (ORCID: https://orcid.org/0000-0002-4086-6453)
- Oren Pasvolsky (ORCID: https://orcid.org/0000-0001-9193-0059)
- Paul Lin (ORCID: https://orcid.org/0000-0002-0524-267X)
- Partow Kebriaei
- R. Champlin
- Denái R. Milton
Institutions
- Dalhousie University (CA)
- The University of Texas MD Anderson Cancer Center (US)
Publication Details
- Journal
- Blood Cancer Journal
- Published
- 2024-10-31
- DOI
- https://doi.org/10.1038/s41408-024-01165-w
- Citations
- 7
- Primary Topic
- Multiple Myeloma Research and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 3.18
Funders
- Leukemia and Lymphoma Society
- Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
- University of Texas MD Anderson Cancer Center
- National Cancer Institute