Dactinomycin in acute myeloid leukemia with NPM1 mutations

被引:11
作者
Beziat, Guillaume [1 ]
Tavitian, Suzanne [1 ]
Bertoli, Sarah [1 ,2 ]
Huguet, Francoise [1 ]
Largeaud, Laetitia [2 ,3 ]
Luquet, Isabelle [3 ]
Vergez, Francois [3 ]
Rieu, Jean-Baptiste [3 ]
Bories, Pierre [4 ]
Delabesse, Eric [2 ,3 ]
Recher, Christian [1 ,2 ]
机构
[1] CHU Toulouse, Inst Univ Canc Toulouse Oncopole, Serv Hematologle, Toulouse, France
[2] Univ Toulouse III Paul Sabatier, Toulouse, France
[3] CHU Toulouse, Inst Univ Canc Toulouse Oncopole, Lab Hematol, Toulouse, France
[4] Inst Univ Canc Toulouse Oncopole, Reseau Oncooccitanie, Toulouse, France
关键词
acute myeloid leukemia; dactinomycin; NPM1; mutations; targeted therapy; AML;
D O I
10.1111/ejh.13438
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Complete responses have been observed in NPM1-mutated AML patients with dactinomycin, a nucleolar stress-inducing drug. Here, we report a single-center experience of compassionate use of dactinomycin in untreated or relapsed/ refractory NPM1-mutated AML. Methods From September 2015 to February 2019, 26 adult patients with NPM1-mutated AML received dactinomycin in different situations: front-line treatment in 4 unfit patients (16%); morphologic (n = 16, 62%), molecular relapses (n = 4, 16%), refractory disease (n = 1, 13%), or postremission therapy in second complete response (n = 1, 13%). Results Median age was 62.5 years. Median number of dactinomycin cycle was 1 (1-8), and 7 patients (27%) received more than 3 cycles. Three out of 17 patients (18%) in morphologic relapse or refractory to chemotherapy achieved complete remission after the first cycle of dactinomycin. None of the 4 patients unfit for intensive chemotherapy responded to dactinomycin as front-line therapy. Grade 3-4 adverse events were thrombocytopenia (n = 11, 42%), neutropenia (n = 11, 42%), GI toxicity (n = 6, 23%), mucositis (n = 5, 19%), lung infection (n = 5, 19%), and skin rash (n = 2, 7.6%). Conclusions Dactinomycin is an inexpensive and easily available drug that may induce significant responses in few AML patients with NPM1 mutations with an acceptable safety profile.
引用
收藏
页码:302 / 307
页数:6
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