The Impact of Melphalan Conditioning and <scp>CD34</scp><sup>+</sup> Cell Dose and Schedule on Post‐Transplant Outcomes in <scp>AL</scp> Amyloidosis
The optimal conditioning schedule and CD34+ cell dose for autologous stem cell transplantation (ASCT) for AL amyloidosis is unknown. Patients (n = 1704) who underwent ASCT for AL amyloidosis between 2003 and 2020 in 9 centers were included. Data on melphalan conditioning dose, number of conditioning days, whether a rest day between conditioning and stem cell infusion was given or not, and infused CD34<sup>+</sup> cell dose were collected. Full-dose melphalan (≥ 180 mg/m<sup>2</sup>) was administered in 63.7% of the patients, and 80.4% had melphalan split into 2-day conditioning. A rest day (day -1) between the conditioning regimen and stem cell infusion was provided in 52.5% of patients. The median infused CD34<sup>+</sup> cell count was 4.7 × 10<sup>6</sup>/kg. An infused CD34<sup>+</sup> cell count ≥ 4.5 × 10<sup>6</sup>/kg was associated with a shorter time to neutrophil and platelet engraftment. In a nominal regression analysis, full-dose melphalan, 1-day melphalan conditioning, and omitting a rest day between conditioning and stem cell infusion were independent predictors of post-ASCT higher deep hematological response. The median follow-up was 8.6 years, and 38% of patients died. Independent predictors of superior overall survival in multivariate Cox regression analysis included full-dose melphalan, having no rest day, and infused CD34<sup>+</sup> cells ≥ 4.5 × 10<sup>6</sup>/kg. Independent predictors of higher day-100 transplant-related mortality (TRM) in nominal logistic regression analysis included poorer performance status, NT-proBNP/BNP ≥ 1800/400 pg/mL, serum albumin < 2.5 g/dL, CD34<sup>+</sup> cells < 4.5 × 10<sup>6</sup>/kg, and not having a rest day. In conclusion, 1 day of melphalan conditioning and administration of CD34<sup>+</sup> cells ≥ 4.5 × 10<sup>6</sup>/kg are recommended for ASCT in AL amyloidosis.
Authors
- Angela A. Dispenzieri (ORCID: https://orcid.org/0000-0001-8780-9512)
- Heather Jolie Landau (ORCID: https://orcid.org/0000-0002-3152-1189)
- David Dingli (ORCID: https://orcid.org/0000-0001-7477-3004)
- Vaishali Sanchorawala (ORCID: https://orcid.org/0000-0002-6307-2445)
- Rajshekhar Chakraborty (ORCID: https://orcid.org/0000-0001-7336-3003)
- Francis K. Buadi (ORCID: https://orcid.org/0000-0003-3214-0203)
- Morie A. Gertz (ORCID: https://orcid.org/0000-0002-3853-5196)
- Muzaffar H. Qazilbash (ORCID: https://orcid.org/0000-0003-2876-2886)
- Caitlin Sarubbi
- Suzanne Lentzsch (ORCID: https://orcid.org/0000-0003-1708-7344)
- Jeffrey A. Zonder (ORCID: https://orcid.org/0000-0002-1741-2795)
- Hila Magen (ORCID: https://orcid.org/0000-0002-3990-394X)
- Sally Arai (ORCID: https://orcid.org/0000-0003-1993-4172)
- Hans Chulhee Lee (ORCID: https://orcid.org/0000-0001-8545-3292)
- Stefan Schönland (ORCID: https://orcid.org/0000-0002-4853-5579)
- Hamza Hassan (ORCID: https://orcid.org/0000-0003-1775-2703)
- Eden Shkury (ORCID: https://orcid.org/0000-0002-1907-8460)
- Andrew Kin
- Michelle M. Chin
- Ute Hegenbart (ORCID: https://orcid.org/0000-0003-1917-6746)
- Eli Muchtar (ORCID: https://orcid.org/0000-0003-2210-2174)
- Eden Mariam Jacob
Institutions
- University of Central Florida (US)
- Boston University (US)
- Boston Medical Center (US)
- Mayo Clinic (US)
- Memorial Sloan Kettering Cancer Center (US)
- The University of Texas MD Anderson Cancer Center (US)
- Tel Aviv University (IL)
- Heidelberg University (DE)
- Columbia University Irving Medical Center (US)
- Sheba Medical Center (IL)
- The Barbara Ann Karmanos Cancer Institute (US)
- Florida College (US)
- Stanford University (US)
Publication Details
- Journal
- American Journal of Hematology
- Published
- 2025-04-11
- DOI
- https://doi.org/10.1002/ajh.27685
- Citations
- 3
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 2.42