Yanada Masamitsu, Matsuo Keitaro, Suzuki Takeshi, Naoe Tomoki
Department of Hematology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Cancer. 2006 Jun 15;106(12):2657-63. doi: 10.1002/cncr.21932.
The prognosis for adult patients with acute lymphoblastic leukemia (ALL) remains unsatisfactory primarily because of the high incidence of recurrence. Therefore, optimal postremission therapy is a matter of vital concern. In particular, the clinical efficacy of allogeneic hematopoietic stem cell transplantation (HSCT) should be clarified.
Rigorous criteria were used to select 7 studies of adult ALL that prospectively assessed overall survival (OS) using natural randomization based on donor availability combined with intention-to-treat analyses. The authors then performed a metaanalysis to evaluate the role of allogeneic HSCT.
Seven studies that included 1274 patients were selected. A metaanalysis demonstrated that patients in the donor groups had significantly better survival than patients in the no-donor groups (hazard ratio [HR], 1.29; 95% confidence interval [95% CI], 1.02-1.63 [P = .037]). When only high-risk patients were included in the analysis, the superiority of the survival advantage was even greater (HR, 1.42; 95% CI, 1.06-1.90 [P = .019]). A meta-regression analysis revealed that compliance with allogeneic HSCT showed a significant and positive correlation with survival (coefficient, 0.022; P < .01), suggesting that the greater the proportion of patients who actually received allogeneic HSCT, the better the survival of the donor group. No beneficial effects of autologous HSCT were observed.
The current findings demonstrated that allogeneic HSCT improves the outcome of adult patients with high-risk ALL. Although these analyses were based on abstracted data, the results indicated that allogeneic HSCT should be considered for such patients if a suitable donor is available.
成年急性淋巴细胞白血病(ALL)患者的预后仍然不尽人意,主要原因是复发率高。因此,缓解后最佳治疗是至关重要的问题。特别是,异基因造血干细胞移植(HSCT)的临床疗效需要明确。
采用严格标准选择7项成年ALL研究,这些研究基于供体可用性通过自然随机化前瞻性评估总生存期(OS)并结合意向性分析。作者随后进行荟萃分析以评估异基因HSCT的作用。
选择了包括1274例患者的7项研究。荟萃分析表明,供体组患者的生存率显著高于无供体组患者(风险比[HR],1.29;95%置信区间[95%CI],1.02 - 1.63 [P = 0.037])。当分析仅纳入高危患者时,生存优势更为明显(HR,1.42;95%CI,1.06 - 1.90 [P = 0.019])。荟萃回归分析显示,异基因HSCT的依从性与生存率呈显著正相关(系数,0.022;P < 0.01),表明实际接受异基因HSCT的患者比例越高,供体组的生存率越好。未观察到自体HSCT的有益效果。
目前的研究结果表明,异基因HSCT可改善成年高危ALL患者的预后。尽管这些分析基于摘要数据,但结果表明,如果有合适的供体,此类患者应考虑进行异基因HSCT。