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日本复发性或原发性难治性儿童淋巴细胞性淋巴瘤的回顾性分析。

Retrospective analysis of relapsed or primary refractory childhood lymphoblastic lymphoma in Japan.

作者信息

Mitsui Tetsuo, Mori Tetsuya, Fujita Naoto, Inada Hiroko, Horibe Keizo, Tsurusawa Masahito

机构信息

Department of Pediatrics, Yamagata University Hospital, Yamagata, Japan.

出版信息

Pediatr Blood Cancer. 2009 May;52(5):591-5. doi: 10.1002/pbc.21941.

Abstract

BACKGROUND AND PROCEDURE

To assess the clinical course with response to second-line treatment and to evaluate the role of hematopoietic stem cell transplantation (SCT) in children with relapsed or primary refractory lymphoblastic lymphoma (LBL), we analyzed data of 48 patients with relapsed/primary refractory diseases among 260 LBL patients identified in a national survey of 1996-2004.

RESULTS

Twenty-six patients achieved second complete remission; 9 achieved partial remission. Of 13 patients who showed progression despite first and second line therapy, only one patient was alive on the second relapse after unrelated cord blood transplantation. Among 40 relapsed patients, the median time between initial diagnosis and relapse was 12.5 months (range 3-56 months). The sites of relapse were isolated BM (n = 9), primary local site with BM (9), primary local site (6), isolated CNS (4), local site with mediastinum (4), primary local site with other site (4), and others (4). Of all 48 patients, 3 were alive after chemotherapy alone. Of the 33 patients, 14 were alive after high dose chemotherapy (HDC)/SCT. With a 27.5-month median follow up period, the 3-year OS rate was 43.2 +/- 7.4% (estimate +/- SE). Univariate analysis identified two features (relapse within 12 months, T cell phenotype) as significant variables that predicted poor survival. Multivariate analysis showed novel statistically significant variables including relapse within 12 months from initial diagnosis (Hazard ratio 3.60) and absence of HDC/SCT (2.64).

CONCLUSION

Outcomes of patients with relapsed/primary refractory LBL were poor, but HDC/SCT for these patients was associated with good results.

摘要

背景与方法

为评估二线治疗反应的临床病程,并评价造血干细胞移植(SCT)在复发或原发性难治性淋巴细胞白血病(LBL)患儿中的作用,我们分析了1996 - 2004年全国性调查中确诊的260例LBL患者中48例复发/原发性难治性疾病患者的数据。

结果

26例患者实现第二次完全缓解;9例实现部分缓解。在13例尽管接受了一线和二线治疗仍出现病情进展的患者中,只有1例在无关脐血移植后的第二次复发时存活。在40例复发患者中,初始诊断与复发之间的中位时间为12.5个月(范围3 - 56个月)。复发部位包括孤立性骨髓(n = 9)、伴有骨髓的原发性局部部位(9)、原发性局部部位(6)、孤立性中枢神经系统(4)、伴有纵隔的局部部位(4)、伴有其他部位的原发性局部部位(4)以及其他(4)。在所有48例患者中,3例仅接受化疗后存活。在33例患者中,14例在接受大剂量化疗(HDC)/SCT后存活。中位随访期为27.5个月,3年总生存率为43.2 +/- 7.4%(估计值 +/- 标准误)。单因素分析确定两个特征(12个月内复发、T细胞表型)为预测生存不良的显著变量。多因素分析显示具有统计学意义的新变量包括初始诊断后12个月内复发(风险比3.60)和未接受HDC/SCT(2.64)。

结论

复发/原发性难治性LBL患者的预后较差,但这些患者接受HDC/SCT可取得较好疗效。

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