First-Line Chemotherapy Leads to High Bone Turnover and Reduced Bone Mass in Patients with Non-Hodgkin's Lymphoma (NHL)

Autor: Panayiotis Panayiotidis, Evangelos Terpos, Athanasios Papatheodorou, Maria K. Angelopoulou, Stavroula Masouridou, Panayiotis Kokkoris, Maria Dimou, Konstantinos Tsionos, Georgios Boutsikas, Dimitrios Christoulas, Theodoros P. Vassilakopoulos, Konstantinos Anargyrou
Rok vydání: 2009
Předmět:
Zdroj: Blood. 114:1951-1951
ISSN: 1528-0020
0006-4971
Popis: Abstract 1951 Poster Board I-974 Chemotherapy associated osteoporosis is a severe problem in patients with malignant diseases as it increases the risk for fractures and deteriorates quality of life. There are very limited data in the literature for the effect of chemotherapy on bone metabolism of adult patients with NHL. To elucidate this issue we scheduled a prospective study in which patients with newly-diagnosed NHL had a thorough evaluation of bone remodeling pre- and post- first-line chemotherapy. As of June 2009, 33 (20M/13F, median age 61 years, range: 28-90 years) of 52 patients, who were entered into this study, had completed their chemotherapeutic scheme: 19 patients (57%) had diffuse large B-cell lymphoma, 5 (15%) follicular lymphoma (grade III), 4 (12%) mantle-cell lymphoma, 4 marginal-zone lymphoma and one T-cell NHL. Twelve (36%) of those had stage IV disease and 17 (51%) had B-symptoms before therapy. Twenty-six patients (78%) received R-CHOP (25 every 21 days and 5 every 14 days), 2 received R-COP and one CHOP as first-line therapy for their disease. Bone mineral density (BMD) of the lumbar spine (L1-L4, antero-posterior view), and femoral neck (FN) was measured by dual energy X-ray absorptiometry (DXA) using a Hologic QDR-1000 scanner on day 1 of cycle 1 (baseline) and on day 30 post the last cycle of chemotherapy. The following serum indices of bone metabolism were measured on the days of DXA: i) osteoclast stimulators [sRANKL and osteoprotegerin (OPG)], ii) osteoblast inhibitor dickkopf-1 (Dkk-1), iii) bone resorption markers [C-telopeptide of collagen type-I (CTX) and tartrate-resistant acid phosphatase-5b (TRACP-5b)], and iv) bone formation markers [bone alkaline phosphatase (bALP) and osteocalcin (OC)]. The above markers were also evaluated in 24 healthy controls of similar gender and age. Patients were assessed for skeletal-related events (SREs) throughout the period of the study. At baseline, NHL patients had a median T-score of L1-L4 BMD of -0.65 (range -4.27 to +3.68) and of FN BMD of -1.1 (-4.01 to +0.2). The median T-score of the lumbar vertebra with the major bone loss was -1.44 (-4.6 to +3.03). At baseline patients had increased levels of Dkk-1 (p=0.036) and reduced levels of OC (p55 years (p=0.007) compared to all others (p=0.059). This reduction was irrespective of the NHL stage (I/II vs. III/IV), while patients who received 8 cycles of chemotherapy had a greater reduction of L1-L4 (p Disclosures: No relevant conflicts of interest to declare.
Databáze: OpenAIRE