Adding Oral Pioglitazone to Standard Induction Chemotherapy of Acute Myeloid Leukemia: A Randomized Clinical Trial

被引:18
作者
Ghadiany, Mojtaba [1 ]
Tabarraee, Mahdi [1 ]
Salari, Sina [1 ]
Haghighi, Shirin [1 ]
Rezvani, Hamid [1 ]
Ghasemi, Seyedeh Najmeh [1 ]
Karimi-Sari, Hamidreza [2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Dept Hematol & Med Oncol, Daneshjoo Blvd,Daneshjoo Sq, Tehran, Iran
[2] Baqiyatallah Univ Med Sci, Student Res Comm, Tehran, Iran
关键词
Drug efficacy; Drug safety; Leucocythaemia; Remission induction; Thiazolidinediones; ACTIVATED RECEPTOR-GAMMA; PPAR-GAMMA; TRITERPENOID CDDO; GROWTH-INHIBITION; CELL-GROWTH; APOPTOSIS; DIFFERENTIATION; EXPRESSION; LIGANDS; KINASE;
D O I
10.1016/j.clml.2019.01.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In an evaluation of the effect of adding pioglitazone to chemotherapy in acute myeloid leukemia (AML) patients, pioglitazone was found to increase the remission rate in AML patients compared to controls. Pioglitazone could have benefits as an adjuvant therapy for AML patients and causes no serious adverse events. Background: The hypothesis of an effect by thiazolidinedione on leukemia cells was proposed 2 decades ago, but there is little clinical evidence regarding its efficacy. We evaluated the safety and efficacy of adding pioglitazone to standard induction chemotherapy in patients with acute myeloid leukemia (AML). Patients and Methods: In this randomized clinical trial, newly diagnosed AML patients were randomized to 1 of 2 groups. Patients in both groups received cytarabine (100 mg/m(2) per day for 7 days) and daunorubicin (60 mg/m(2) per day for 3 days). Patients in the pioglitazone group additionally received oral pioglitazone (45 mg per day). The 2 groups were compared according to remission rate, laboratory findings, and adverse events during treatment. Results: Forty patients were evaluated, 20 patients in each group. The complete remission rate was 20% more in the pioglitazone group compared to the control group (P = .202). Complications due to pioglitazone discontinuation were observed in 2 cases. The mean serum alanine aminotransferase in the fourth treatment week was significantly more in pioglitazone group compared to the control group (65.5 vs. 33.6 mg/dL, P = .039). The mean serum creatinine in all treatment phases was significantly higher in the pioglitazone group compared to the control group (P < .05). There were no significant differences between the 2 groups regarding other laboratory findings (P > .05). Conclusion: Adding pioglitazone to cytarabine and daunorubicin increased the remission rate in AML patients compared to control subjects. Although this difference in remission rate between the 2 groups was not statistically significant, it could be important in the clinical setting. Pioglitazone may provide benefits as an adjuvant therapy for AML patients without causing serious adverse events.
引用
收藏
页码:206 / 212
页数:7
相关论文
共 30 条
[1]   Rosiglitazone enhances radiosensitivity by inhibiting repair of DNA damage in cervical cancer cells [J].
An, Zhengzhe ;
Yu, Jae-Ran ;
Park, Woo-Yoon .
RADIATION AND ENVIRONMENTAL BIOPHYSICS, 2017, 56 (01) :89-98
[2]  
[Anonymous], EUR J NUTR
[3]  
[Anonymous], J STEROID BIOCH MOL
[4]  
Arashnia Rana, 2015, J Nephropathol, V4, P48, DOI 10.12860/jnp.2015.10
[5]   Inhibition of Age-Related Therapy Resistance in Melanoma by Rosiglitazone-Mediated Induction of Klotho [J].
Behera, Reeti ;
Kaur, Amanpreet ;
Webster, Marie R. ;
Kim, Suyeon ;
Ndoye, Abibatou ;
Kugel, Curtis H., III ;
Alicea, Gretchen M. ;
Wang, Joshua ;
Ghosh, Kanad ;
Cheng, Phil ;
Lisanti, Sofia ;
Marchbank, Katie ;
Dang, Vanessa ;
Levesque, Mitchell ;
Dummer, Reinhard ;
Xu, Xiaowei ;
Herlyn, Meenhard ;
Aplin, Andrew E. ;
Roesch, Alexander ;
Caino, Cecilia ;
Altieri, Dario C. ;
Weeraratna, Ashani T. .
CLINICAL CANCER RESEARCH, 2017, 23 (12) :3181-3190
[6]   Revised recommendations of the international working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for therapeutic trials in acute myeloid leukemia [J].
Cheson, BD ;
Bennett, JM ;
Kopecky, KJ ;
Büchner, T ;
Willman, CL ;
Estey, EH ;
Schiffer, CA ;
Döhner, H ;
Tallman, MS ;
Lister, TA ;
LoCocco, F ;
Willemze, R ;
Biondi, A ;
Hiddemann, W ;
Larson, RA ;
Löwenberg, B ;
Sanz, MA ;
Head, DR ;
Ohno, R ;
Bloomfield, CD .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) :4642-4649
[7]   A novel ring-substituted diindolylmethane, 1,1-bis[3′-(5-methoxyindolyl)]-1-(p-t-butylphenyl) methane, inhibits extracellular signal-regulated kinase activation and induces apoptosis in acute myelogenous leukemia [J].
Contractor, R ;
Samudio, IJ ;
Estrov, Z ;
Harris, D ;
McCubrey, JA ;
Safe, SH ;
Andreeff, M ;
Konopleva, M .
CANCER RESEARCH, 2005, 65 (07) :2890-2898
[8]   Activation of PPARγ by endogenous prostaglandin J2 mediates the antileukemic effect of selenium in murine leukemia [J].
Finch, Emily R. ;
Tukaramrao, Diwakar B. ;
Goodfield, Laura L. ;
Quickel, Michael D. ;
Paulson, Robert F. ;
Prabhu, K. Sandeep .
BLOOD, 2017, 129 (13) :1802-1810
[9]   PPARγ ligands increase antileukemic activity of second- and third-generation tyrosine kinase inhibitors in chronic myeloid leukemia cells [J].
Glodkowska-Mrowka, E. ;
Manda-Handzlik, A. ;
Stelmaszczyk-Emmel, A. ;
Seferynska, I. ;
Stoklosa, T. ;
Przybylski, J. ;
Mrowka, P. .
BLOOD CANCER JOURNAL, 2016, 6 :e377-e377
[10]   PPAR targeted oral cancer treatment and additional utility of genomics analytic techniques [J].
Handley, Nathan ;
Eide, Jacob ;
Taylor, Randall ;
Wuertz, Beverly ;
Gaffney, Patrick ;
Ondrey, Frank .
LARYNGOSCOPE, 2017, 127 (04) :E124-E131