de la Rubia Javier, Bladé Joan, Lahuerta Juan-José, Ribera Josep M, Martínez Rafael, Alegre Adrián, García-Laraña José, Fernández Pascual, Sureda Anna, de Arriba Felipe, Carrera Dolores, Besalduch Joan, García Boyero Raimundo, Palomera Bernal Luis, Hernández Miguel T, García Paz Ribas, Pérez-Calvo Javier, Alcalá Antonio, Casado Luis Felipe, San Miguel Jesús
Grupo Español de Mieloma.
Haematologica. 2006 May;91(5):621-7. Epub 2006 Apr 19.
Although alkylating agents are clearly beneficial in multiple myeloma (MM), their deleterious effect on bone marrow hematopoietic progenitor cells usually precludes their use as front-line therapy in patients scheduled to undergo autologous stem cell transplantation (ASCT). We analyzed the impact of first-line chemotherapy with alkylating agents on stem cell collection in MM patients.
Seven hundred and eighty-nine patients included in the Spanish multicenter protocol GEM-2000 underwent mobilization therapy after four courses of alternating VBMCP/VBAD chemotherapy.
The mobilization regimens consisted of standard or high-dose granulocyte colony-stimulating factor (G-CSF) in 551 (70%) patients, and chemotherapy and G-CSF in 206 (26%) patients. The CD34+ cell yield was lower than 4x10(6)/kg in 388 patients (49%), and equal or greater than 4x10(6)/kg in 401 patients (51%). Multivariate analysis indicated that advanced age (p<0.0001) and longer interval between diagnosis and mobilization (p=0.012) were the two variables associated with a lower CD34+ cell yield. Significant differences in CD34+ cell yield were not observed between the mobilization regimens. Of the 789 patients included in the protocol, 726 (92%) underwent the planned ASCT, whereas 25 (3%) patients did not because of the low number of CD34+ cells collected. Following ASCT, 0.5x10(9) neutrophils/L could be recovered after 11 days (median time; range, 5-71 days) and 20x10(9) platelets/L could be recovered after 12 days (median time; range, 6-69 days).
A short-course of therapy with alkylating agents according to the GEM-2000 protocol was associated with an appropriate CD34+ cell collection, and allowed the planned ASCT to be performed in the majority of MM patients.
尽管烷化剂在多发性骨髓瘤(MM)治疗中益处明显,但其对骨髓造血祖细胞的有害作用通常使其无法用于计划进行自体干细胞移植(ASCT)的患者的一线治疗。我们分析了MM患者一线使用烷化剂化疗对干细胞采集的影响。
纳入西班牙多中心方案GEM - 2000的789例患者在接受四个疗程的交替VBMCP/VBAD化疗后接受动员治疗。
动员方案包括551例(70%)患者采用标准或高剂量粒细胞集落刺激因子(G - CSF),206例(26%)患者采用化疗联合G - CSF。388例患者(49%)的CD34 +细胞产量低于4×10⁶/kg,401例患者(51%)的CD34 +细胞产量等于或高于4×10⁶/kg。多因素分析表明,高龄(p < 0.0001)和诊断与动员之间的间隔时间较长(p = 0.012)是与较低的CD34 +细胞产量相关的两个变量。不同动员方案之间未观察到CD34 +细胞产量的显著差异。该方案纳入的789例患者中,726例(92%)接受了计划的ASCT,而25例(3%)患者因采集的CD34 +细胞数量少未进行。ASCT后,11天(中位时间;范围5 - 71天)可恢复至0.5×10⁹/L中性粒细胞,12天(中位时间;范围6 - 69天)可恢复至20×10⁹/L血小板。
按照GEM - 2000方案进行的短疗程烷化剂治疗与适当的CD34 +细胞采集相关,并使大多数MM患者能够进行计划的ASCT。