Tarella C, Di Nicola M, Caracciolo D, Zallio F, Cuttica A, Omedè P, Bondesan P, Magni M, Matteucci P, Gallamini A, Pileri A, Gianni A M
Dip Med Oncol Sperimentale, Div Univ Ematologia, AO S Giovanni B, Torino, Italy.
Bone Marrow Transplant. 2002 Dec;30(11):725-32. doi: 10.1038/sj.bmt.1703729.
A high-dose (HD) chemotherapy scheme was designed for the collection of large numbers of peripheral blood progenitor cells (PBPC) in lymphoma patients who were candidates for myeloablative therapy with autograft. The scheme included the sequential administration of HD cyclophosphamide (CY) (7 g/m(2)) and HD ara-C (2 g/m(2) twice a day for 6 consecutive days), followed by final consolidation with PBPC autograft. PBPC harvests were scheduled following both HD CY and HD ara-C. To minimize hematologic toxicity, small aliquots of PBPC (<or=3 x 10(6) CD34(+) cells/kg) collected following HD CY were reinfused following HD ara-C. The treatment was delivered to 112 patients (median age: 43 years) with lymphoid malignancies (107 non-Hodgkin's lymphoma, four Hodgkin's lymphoma, one amyloidosis); 75 patients were at disease onset, whereas 37 had relapsed or were refractory after first-line conventional therapy. PBPC mobilization was assessed in terms of peak values of circulating CD34(+) cells/microl, as well as total CD34(+) cells/kg collected. In a few patients CFU-GM/kg were also evaluated. At the time of maximal mobilization following HD CY, 93 'high-mobilizer' patients had >20 circulating CD34(+) cells/microl, whereas the remaining 19 'low-mobilizer' patients did not reach this cut-off value. In spite of poor mobilization after HD CY, 16 out of 19 low mobilizers provided good harvests following HD ara-C; overall, median collected CD34(+) cells x 10(6)/kg were 1.4 (0-3.1) and 10.2 (0-37) after HD CY and HD ara-C, respectively (P = 0.00007). Similar patterns were observed when PBPC were evaluated by CFU-GM/kg. Complete and durable hemopoietic reconstitution followed autograft with post HD ara-C PBPC. Within the high-mobilizer group, 88 patients received HD ara-C and 79 (90%) still showed high mobilization; overall, median collected CD34(+)cells x 10(6)/kg were 17.8 (range 3-94) and 19 (range 0-107) after HD CY and HD ara-C respectively (P = NS). Thus, the scheme allowed sufficient PBPC collections for autografting in low mobilizer patients; in addition, the scheme could be considered whenever extensive chemotherapy debulking is needed prior to PBPC collection.
设计了一种高剂量(HD)化疗方案,用于采集大量外周血祖细胞(PBPC),这些细胞来自适合进行清髓性自体移植治疗的淋巴瘤患者。该方案包括序贯给予高剂量环磷酰胺(CY)(7 g/m²)和高剂量阿糖胞苷(HD ara-C)(2 g/m²,每日两次,连续6天),随后进行PBPC自体移植的最终巩固治疗。PBPC采集安排在HD CY和HD ara-C之后。为了将血液学毒性降至最低,在HD CY后采集的少量PBPC(≤3×10⁶ CD34⁺细胞/kg)在HD ara-C后回输。该治疗应用于112例(中位年龄:43岁)淋巴系统恶性肿瘤患者(107例非霍奇金淋巴瘤、4例霍奇金淋巴瘤、1例淀粉样变性);75例患者处于疾病初发期,而37例在一线常规治疗后复发或难治。根据循环中CD34⁺细胞/μl的峰值以及采集的总CD34⁺细胞/kg来评估PBPC动员情况。在少数患者中还评估了CFU-GM/kg。在HD CY后最大动员时,93例“高动员者”患者循环中CD34⁺细胞/μl>20,而其余19例“低动员者”患者未达到该临界值。尽管HD CY后动员不佳,但19例低动员者中有16例在HD ara-C后获得了良好的采集量;总体而言,HD CY和HD ara-C后采集的CD34⁺细胞×10⁶/kg中位数分别为1.4(0 - 3.1)和10.2(0 - 37)(P = 0.00007)。当通过CFU-GM/kg评估PBPC时观察到类似模式。HD ara-C后的PBPC自体移植后实现了完全且持久的造血重建。在高动员者组中,88例患者接受了HD ara-C,79例(90%)仍表现出高动员;总体而言,HD CY和HD ara-C后采集的CD34⁺细胞×10⁶/kg中位数分别为17.8(范围3 - 94)和19(范围0 - 107)(P = 无显著差异)。因此,该方案能够为低动员者患者采集足够的PBPC用于自体移植;此外,每当在PBPC采集前需要进行广泛的化疗减瘤时,都可以考虑该方案。