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化疗与吉妥珠单抗奥唑米星联合用于表达CD33的成人费城染色体阳性急性淋巴细胞白血病患者。

Combination of chemotherapy and gemtuzumab ozogamicin in adult Philadelphia positive acute lymphoblastic leukemia patient harboring CD33 expression.

作者信息

Chevallier Patrice, Mahe Beatrice, Garand Richard, Talmant Pascaline, Harousseau Jean-Luc, Delaunay Jacques

机构信息

Department of Hematology, Centre Hospitalier Universitaire, Nantes, France.

Service d'Hématologie Clinique, Centre Hospitalier Universitaire, 9 quai Moncousu, BP1005, 44093, Nantes cedex 01, France.

出版信息

Int J Hematol. 2008 Sep;88(2):209-211. doi: 10.1007/s12185-008-0123-2. Epub 2008 Aug 1.

DOI:10.1007/s12185-008-0123-2
PMID:18668307
Abstract

Gemtuzumab Ozogamicin (GO) is a humanized anti-CD33 antibody conjugated with a cytotoxic antitumor antibiotic, calicheamicin-g1. It was developed at the end of the nineties as 90% of the leukemic blast population of patients with acute myeloid leukaemia (AML) express the CD33 surface antigen (Dinndorf et al. [1] Blood 1986;67:1048-53). GO is currently approved in monotherapy for the treatment of CD33+ AML patients in first relapse, showing a 26% overall response rate and a median disease-free-survival of 5.2 months for responders (Larson et al. [2] Cancer 2005;104:1442-52). CD33 antigen expression is also observed at diagnosis (in 15% of cases) (Pui et al. [3] J Clin Oncol 1998;16:3768-73) or at relapse (Guglielmi et al. [4] Leukemia 1997; 11:1501-7) of acute lymphoblastic leukaemia (ALL), representing a potential cellular target for ALL patients. Case series have already demonstrated the efficacy of GO in children with relapsed CD33+ ALL with documentation of complete remission (CR) (Balduzzi et al. [5] Leukemia 2003;17:2247-8; Cotter et al. [6] Br J Haematol 2003;122:686-91; Zwaan et al. [7] Leukemia 2003;17:468-70). In the other hand, there is no report at our knowledge of the use of GO in the setting of adult CD33+ ALL patient. Here we report the case of a 30-year-old man with a refractory CD33+ ALL who received a salvage regimen combining chemotherapy + GO and achieved a transient CR.

摘要

吉妥单抗奥唑米星(GO)是一种与细胞毒性抗肿瘤抗生素刺孢霉素 - g1偶联的人源化抗CD33抗体。它于九十年代末研发,因为90%的急性髓系白血病(AML)患者的白血病原始细胞群表达CD33表面抗原(Dinndorf等人[1]《血液》1986年;67:1048 - 53)。GO目前被批准用于一线复发的CD33 + AML患者的单药治疗,显示出26%的总缓解率,缓解者的无病生存期中位数为5.2个月(Larson等人[2]《癌症》2005年;104:1442 - 52)。在急性淋巴细胞白血病(ALL)的诊断时(15%的病例)(Pui等人[3]《临床肿瘤学杂志》1998年;16:3768 - 73)或复发时(Guglielmi等人[4]《白血病》1997年;11:1501 - 7)也观察到CD33抗原表达,这代表了ALL患者的一个潜在细胞靶点。病例系列已经证明GO对复发的CD33 + ALL儿童有效,有完全缓解(CR)的记录(Balduzzi等人[5]《白血病》2003年;17:2247 - 8;Cotter等人[6]《英国血液学杂志》2003年;122:686 - 91;Zwaan等人[7]《白血病》2003年;17:468 - 70)。另一方面,据我们所知,尚无关于在成年CD33 + ALL患者中使用GO的报道。在此我们报告一例30岁难治性CD33 + ALL男性患者的病例,该患者接受了化疗 + GO联合的挽救方案并实现了短暂的CR。

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