All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional. If you are a patient or carer, please visit the International Myeloma Foundation or HealthTree for Multiple Myeloma.
The Multiple Myeloma Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the Multiple Myeloma Hub cannot guarantee the accuracy of translated content. The Multiple Myeloma Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The Multiple Myeloma Hub is an independent medical education platform, sponsored by Bristol Myers Squibb, GSK, Legend Biotech, Pfizer, and Roche. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account and access these new features:
Bookmark content to read later
Select your specific areas of interest
View multiple myeloma content recommended for you
Real-world results from a retrospective, multicenter study, evaluating autologous stem cell boost (auto-SCB) for chimeric antigen receptor T-cell (CAR T)-related hematologic toxicity in adults with relapsed/refractory multiple myeloma (RRMM), were published in Blood Cancer Journal by Varga et al. Outcomes were compared between patients with prolonged cytopenias receiving SCB within 1 year of CAR T-cell infusion (n = 39) and matched controls receiving supportive care (no SCB; n = 52).
Key data: Auto-SCB led to hematologic recovery in 97.4% of patients, with a median time to recovery of 24 days. At Day 90, SCB patients had higher median hemoglobin (10.6 vs 8.7 g/dL; p = 0.002) and platelet counts (135 vs 35 K/µL; p < 0.001) vs non-SCB controls. Median progression-free survival (PFS) was 11.0 months with SCB vs 8.2 months with no SCB, while median overall survival (OS) was not reached (NR) and 12.3 months, respectively. No new toxicities were attributed to SCB.
Key learning: Auto-SCB was shown to be a well-tolerated and effective strategy to promote hematologic recovery in patients with RRMM experiencing prolonged cytopenias after CAR T-cell therapy, supporting its consideration as a supportive strategy for selected patients.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content