Method: We designed a prospective, observational study which enrolled 100 patients undergoing HSCT (60% autologous, 40% allogeneic. 19 unrelated, 13 sibling, 8 double cord. Myeloma 44%, leukemia 29%, lymphomas 26%, and aplastic anemia 1%). Patients enrolling on the study completed 5 questionnaires before HSCT and 1, 2, 3, 6, 9, and 12 months after HSCT. The questionnaires were the Brief Pain Inventory (BPI), the EORTC Quality of Life Questionnaire-Chemotherapy Induced Peripheral Neuropathy (EORTC-CIPN), the Muscle and Joint Measure (MJM), the MD Anderson Symptom Index – Graft-versus-Host Disease module (MDASI-cGVHD), and the Hospital Anxiety and Depression Scale (HADS).
Results: At the 9-month review, we found that there was a significant increase in pain reported after allogeneic HSCT compared to pre-HSCT. (71% increase at 3 months; p=0.01). This difference was independent of conditioning regimen, disease or GVHD. For autologous HSCT, there was an increase in reported neuropathic symptoms (47% increase at 3 months; p=0.02). We also found and increase in muscle cramping and spasms late after HSCT; both autologous and allogeneic (99% increase at 9 months; p=0.03). Muscle cramping interfered with sitting, standing and physical activity (21% at 6 months; p=0.04 and 136% at 9 months; p=0.04). The increase in muscle cramping symptoms was independent of conditioning regimen, disease or GVHD.
Conclusions: Our current review of this study reveals that pain and muscle cramping is a significant symptom that develops after both allogeneic and autologous HSCT. This appears to be independent of conditioning regimen, disease or GVHD.