|Year : 2019 | Volume
| Issue : 2 | Page : 167-172
Efficacy of high-dose cytarabine and aclarubicin in combination with G-CSF regimen compared to intermediate/high-dose cytarabine and standard-dose cytarabine induction regimen for non-remission acute myeloid leukemia
Meiqing Lei1, Limin Liu2, Zhiming Wang3, Depei Wu2
1 Department of Hematology in the First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology, Collaborative Innovation Center of Hematology, Suzhou Institute of Blood and Marrow Transplantation, Suzhou; Department of Hematology in Haikou Municipal People's Hospital, Affiliated Haikou Hospital Xiangya School of Medicine Central South University, Haikou, China
2 Department of Hematology in the First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology, Collaborative Innovation Center of Hematology, Suzhou Institute of Blood and Marrow Transplantation, Suzhou, China
3 Department of Hematology in Haikou Municipal People's Hospital, Affiliated Haikou Hospital Xiangya School of Medicine Central South University, Haikou, China
|Date of Web Publication||2-May-2019|
Department of Hematology in the First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology, Collaborative Innovation Center of Hematology, Suzhou Institute of Blood and Marrow Transplantation, Suzhou
Source of Support: None, Conflict of Interest: None
BACKGROUND: Acute myeloid leukemia (AML) patients with non-remission (NR) after the first cycle of standard induction chemotherapy remain a challenge owing to poor response and tolerance to re-induction regimen. We retrospectively evaluated the efficacy and safety of three regimens in AML patients refractory to the first course of standard induction regimen.
MATERIALS AND METHODS: The three regimens consisted of (1) High-dose cytarabine, aclarubicin and granulocyte colony-stimulating factor (HD-CAG) regimen (n = 44); (2) intermediate/high-dose cytarabine (I/HDAC) regimen (n = 30); and (3) standard-dose cytarabine (SDAC) combination regimen that was identical to the first course of standard induction regimen (n = 27).
RESULTS: Results indicated that after the second course, the overall response (OR), i.e., complete remission [CR]+partial remission [PR]) rates in HD-CAG was higher than in the I/HDAC group (84.1% vs. 56.7%, P = 0.009), whereas the CR rates among 3 groups were not statistically different (P = 0.541). Meanwhile, the proportion of subjects reporting certain adverse effects in the HD-CAG group was lower than the I/HDAC or SDAC groups. There were no significant differences in overall survival (OS) and disease-free survival (DFS) rates among the 3 groups (P = 0.881 and P = 0.872, respectively).
CONCLUSION: Our preliminary results indicate that HD-CAG regimen may represent a better alternative option for AML patients with NR after the first course of standard induction chemotherapy.
Keywords: Acute myeloid leukemia, high-dose CAG, induction remission, non-remission, re-induction regimen
|How to cite this article:|
Lei M, Liu L, Wang Z, Wu D. Efficacy of high-dose cytarabine and aclarubicin in combination with G-CSF regimen compared to intermediate/high-dose cytarabine and standard-dose cytarabine induction regimen for non-remission acute myeloid leukemia. Indian J Cancer 2019;56:167-72
|How to cite this URL:|
Lei M, Liu L, Wang Z, Wu D. Efficacy of high-dose cytarabine and aclarubicin in combination with G-CSF regimen compared to intermediate/high-dose cytarabine and standard-dose cytarabine induction regimen for non-remission acute myeloid leukemia. Indian J Cancer [serial online] 2019 [cited 2019 May 25];56:167-72. Available from: http://www.indianjcancer.com/text.asp?2019/56/2/167/257556
| » Introduction|| |
The standard anthracycline-plus-cytarabine induction regimen (3 days of anthracycline and 7 days of cytarabine [Ara-C], namely “3+7”) can enable 60–80% of younger adults and 40–50% of older patients with de novo acute myeloid leukemia (AML, excluding acute promyelocytic leukemia) achieve complete remission (CR). However, a significant proportion of AML patients exhibit non-remission (NR) after the first cycle of “3+7” regimen. Unfortunately, there is no standard re-induction regimen for AML patients refractory to “3+7” regimen. According to NCCN Guidelines Version 2.2012 for AML, high-dose cytarabine (HDAC) alone or standard-dose cytarabine (SDAC) with idarubicin or daunorubicin are recommended if patients performance allows these regimens. In fact, I/HDAC regimens were reported to result in a CR rate of 39.1–83%, yet followed by severe myelosuppression and related infection., Meanwhile, SDAC combination regimens were utilized by other treatment groups, whereas the CR rate ranged from 31.1% to 60% in these AML patients.
In 1995, a Japanese group first reported CAG (low-dose cytarabine and aclarubicin and granulocyte-colony-stimulating factor [G-CSF]) regimen for AML treatment. Subsequently, this regimen was widely applied in Japan and China. Recently, a meta-analysis of CAG regimen treatment for 814 new and relapsed/refractory AML patients showed that the overall CR rate of a similar CAG regimen was higher than non-CAG regimens. However, it should be noted that non-CAG regimens and the dosage of aclarubicin of the CAG regimen were varied in the study. Therefore, it is difficult to ascertain whether the inherent variation may influence the results. Therefore, efforts should be made to clarify the exact regimens being compared and explore some CAG-modified strategies. More recently, our clinical center found that increasing the aclarubicin dose in conventional CAG regimen (namely high-dose CAG [HD-CAG]) can improve CR rate of relapsed/refractory AML patients than conventional CAG regimen, with tolerable toxicity., Herein, we performed a retrospective study to evaluate the effectiveness and tolerability of HD-CAG, I/HDAC, and SDAC regimens in these AML patients unresponsive to the first cycle of “3+7” regimen.
| » Materials and Methods|| |
In total, 101 hospitalized AML patients (excluding acute promyelocytic leukemia) were analyzed from October 2006 to September 2015 in our center and Haikou Municipal People's Hospital. All subjects had the following characteristics: (1) newly diagnosed AML de novo with cytogenetic and/or molecular results; (2) refractory to the first course of “3+7” regimen (excluding CR or partial remission (PR); (3) the second protocol had to be HD-CAG, I/HDAC, or SDAC regimen; (4) performance status of 0-3 according to the Eastern Cooperative Oncology Group and without severe function damage of vital organ (cardiac, hepatic, and renal). (5) All subjects were younger than 60 years.
The AML was confirmed by bone marrow (BM) morphologic, immunophenotypic, cytogenetic, and/or molecular analyses according to the World Health Organization 2008 classification criteria. The risk status was according to cytogenetics and molecular genetic abnormalities according to NCCN guidelines Version 2.2012 for AML. All patients were classified as 3 grades: better-risk including t(8;21), and inv(16) or t(16;16)), normal cytogenetics with the NPM1 mutation, and normal cytogenetics with an isolated biallelic CEBPA mutation in absence of FLT3-ITD; intermediate-risk referring to normal cytogenetics, +8, t(9;11) and other non-defined, and t(8;21)/inv16/t(16;16) with c-KIT mutation; and poor-risk defined as complex ≥3 clonal chromosomal abnormalities, -5/5q-, -7/7q-, 11q23 - non t(9;11), inv(3)/t(3;3), t(6;9), t(9;22), and normal cytogenetics with FLT3-ITD mutation.
According to past NCCN guidelines, the recommended AML re-induction therapy after standard-dose cytarabine for patients age <60 year is HDAC alone or SDAC. I/HDAC-based regimens included Ara-C 1–3 g/m2 every 12 h for 4 days. For regimens combining IDAC with anthracyclines (idarubicin/pirarubicin) or non-anthracyclines (mitoxantrone/etoposide), Ara-C was 1–2 g/m2 every 12 h for 4 days. Fludarabine, Ara-C and G-CSF (FLAG) regimen (fludarabine 35 mg/m2 infused intravenously daily from day 1 to 5, Ara-C 2 g/m2 infused intravenously daily from day 1 to 5, and G-CSF administered subcutaneously at a dose of 200 μg/m2/d from days 0 to 5 unless patient WBC count was ≥20 × 109/L). SDAC combination regimens: combining Ara-C with anthracyclines (daunorubicin/idarubicin) or non-anthracyclines (mitoxantrone/homoharringtonine); the dose of Ara-C in all these regimens was 100–200 mg/m2/day for 7 days.
As for other alternatives, it is best to meet the following three criteria: (i) is less toxic than HDAC; (ii) avoids leukemia resistance due to previous SDAC exposure; and (iii) improves the effect of conventional CAG. From this, we evaluated the effect of the HD-CAG regimen as follows: HD-CAG regimen (Ara-C [Actavis Italy S.p.A] 10 mg/m2 injected subcutaneously every 12 h for 14 days, aclarubicin [Yangzhou Pharmaceutical Co., Ltd, China] 5-7 mg/m2/day infused intravenously for 14 days, G-CSF [Qilu Pharmaceutical Co., Ltd, China] 200 μg/m2/d administered subcutaneously for 14 days, unless patient WBC count was ≥20 × 109/L, the administration of G-CSF was postponed, and reused when patient WBC count returned to <20 × 109/L. G-CSF was first administered before the first subcutaneous injection of Ara-C and was stopped 12 h before the last dose of Ara-C.
The choice of re-induction regimen was according to the treating physician's discretion depending the patient's age, comorbidities, and preferences. Chemotherapy-related supportive care was implemented as previously described. CR patients received consolidation therapy. If a suitably matched donor was found, the eligible patients underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT). Without a matched donor, the patients with intermediate/poor-risk status were recommended for haploidentical related-donor HSCT. If patients did not accept HSCT, subsequent consolidation chemotherapy was arranged on time including I/HDAC regimens. Patients with poor performance status were treated with SDAC or low-intensity therapy (subcutaneous Ara-C, 5-azacytidine, and decitabine). The flow diagram is indicated in [Figure 1].
|Figure 1: Treatment scheme of the 101 patients in this study. AML, acute myeloid leukemia; Allo-HSCT, allogeneic hematopoietic stem cell transplantation; IND1, initial standard anthracycline-plus-cytarabine induction chemotherapy; CR, complete remission; PR, Partial remission; NR, Non-remission; 1: HDAC (high-dose cytarabine); 2: IDAC+M/IDA/VP16/THP (intermediate-dose cytarabine plus mitoxantrone/idarubicin/etoposide/pirarubicin); 3: FLAG (fludarabine, cytarabine, and G-CSF); 4: DA/IA (daunorubicin plus cytarabine/idarubicin plus cytarabine); 5: MA/HA (mitoxantrone plus cytarabine/homoharringtonine plus cytarabine); 6: HD-CAG (high-dose cytarabine and aclarubicin in combination with G-SCF regimen)|
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Evaluation of efficacy and toxicity
CR was defined as BM blasts <5%, without blasts with Auer rods More Details, the absence of extra-medullary disease, neutrophil count >1.0 × 109/L, and a platelet count >100 × 109/L. PR was defined as the decrease of BM blasts to 5%-20% in the BM aspirate and normalization of blood counts. Overall response (OR) included CR and PR. NR was defined as not achieving CR or PR after chemotherapy. Refractory to the first course of standard induction chemotherapy was defined as a failure to achieve CR or PR after this regimen. Adverse events were evaluated by the WHO score. Hematological and non-hematological toxicity was observed and recorded by monitoring hemogram, biochemical parameters, and conducting other related auxiliary examinations.
Data were analyzed by SPSS19.0. The independence of the categorical parameters among patient subsets was calculated using the chi-squared test. The distribution of the continuous variables was estimated using the Kruskal-Wallis test. The overall survival (OS) was measured from the date of AML diagnosis to death regardless of any cause, and the surviving patients were followed-up to the conclusion of this study or date of the last contact. The disease-free survival (DFS) was measured from the CR to relapse or death during CR. The Kaplan-Meier analysis was used to analyze OS and DFS rates. Statistical results (P < 0.05) were considered significant.
| » Results|| |
Characteristics of patients and disease
In total, 101 AML patients refractory to the first cycle of standard induction chemotherapy were enrolled in this study. Among them, 44 patients were treated with HD-CAG regimen, 30 patients treated with I/HDAC regimens (HDAC, n = 4; IDAC, n = 4; IDAC+M, n = 3; IDAC+IDA/VP16/THP, n = 3; and FLAG, n = 16), and 27 treated patients with SDAC regimens (DA, n = 1; IA, n = 12; MA, n = 8; and HA, n = 6) [Figure 1]. The respective characteristics of patients are summarized in [Table 1]. There were no significant differences found for age, gender, FAB subtype, risk status, and WBC count onset. The proportion of allo-HSCT among active treatment patients was not different among the 3 groups [Table 1].
Response to re-induction regimens
Despite no differences in CR rate among the 3 groups being found, there were overall significant differences in OR rate (P = 0.032) [Table 1]. Specifically, the OR rate of HD-CAG group was higher than I/HDAC group (84.1% vs. 56.7%, P = 0.009). Moreover, there were no significant differences in OR rates between SDAC and I/HDAC or HD-CAG group (P = 0.169 and P = 0.303, respectively).
Myelosuppression was ubiquitous in all re-induction regimens. Although relatively shorter median duration of neutropenia (neutrophils <0.5 × 109/L) was found in the HD-CAG group, there were no significant differences among the 3 groups (P = 0.140). The median duration of thrombocytopenia (PLTs <50 × 109/L) was similar among the 3 groups. There was also no statistically significant differences in incidence of grade 3–4 leukopenia and thrombocytopenia among the 3 groups (P = 0.590 and P = 0.590, respectively). During neutropenia, infection was common, but there was no difference in the various types of infections (P = 0.051) among the groups. Non-hematological side effects were mild, and two events of severe complications were reported in the I/HDAC group: grade 4 hepatic dysfunction, from which the patient quickly recovered following intensifying supportive treatment and a pneumonia that resulted in a fatality.
In the HD-CAG group (n = 44), 41 patients received subsequent treatment, including allo-HSCT (n = 15; 11 achieving CR, 3 achieving PR, and 1 achieving NR), auto-HSCT (2 achieving CR), and chemotherapy (n = 24). In the I/HDAG group (n = 30), 28 patients received subsequent treatment, including allo-HSCT (n = 17; 11 achieving CR and 6 achieving NR) and chemotherapy (n = 11). In the SDAC group (n = 27), 25 patients received subsequent treatment, including allo-HSCT (n = 9; 6 achieving CR, 3 achieving NR), auto-HSCT (1 achieving CR), and chemotherapy (n = 15) [Figure 1]. In the HD-CAG, I/HDAC, and SDAC groups, the OS rates at 24 months were 39.9% ± 9.3%, 45.2% ± 13.4%, and 35.4% ± 12.5%, whereas the respective DFS rates at 24 months were 53.6% ± 11.1%, 53.6% ± 16.9%, and 55.9% ± 13.7%. There was no differences in OS [P = 0.881, [Figure 2]a], and DFS rates [P = 0.872; [Figure 2]b] were observed among the 3 groups.
|Figure 2: Effect of the three re-induction chemotherapy regimens on overall survival (a) and disease-free survival (b) in AML patient's refractory to initial induction therapy. HD-CAG, high-dose cytarabine, and aclarubicin in combination with G-SCF; I/HDAC, intermediate/high-dose cytarabine; and SDAC, standard-dose cytarabine induction|
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| » Discussion|| |
Reasonable choice of re-induction regimen for these AML patients with failure of “3+7” standard inductive chemotherapy has important clinical implications because it is closely related to subsequent therapeutic options and prognosis. Despite better tolerance of CAG than I/HDAC and SDAC, approximately 40–50% of patients do not achieve CR. Thus, some modified CAG regimens have been explored including combination with decitabine, Fms-like tyrosine kinase 3 inhibitor, or by increasing the dose of aclarubicin.,,
In this study, we enrolled 101 eligible AML patients refractory to the first cycle of “3+7” regimen to compare the efficacy and safety of HD-CAG, I/HDAC, and SDAC regimens. Overall statistic analysis on OR rate revealed significant differences among the 3 groups (P = 0.032). Furthermore, by Chi-square segmentation, the results indicated that the OR rate of HD-CAG regimen was significantly higher than the I/HDAC regimen (P = 0.009), whereas the OR rate of SDAC regimen group was not significant when compared with either HD-CAG or I/HDAC. Moreover, the CR rate was not statistically different among the 3 groups. It is not difficult to infer from the above results that HD-CAG regimen gets a higher percentage of patients achieving PR than I/HDAC and SDAC regimens, which may alleviate the burden of residual leukemia and related complications, and improve patient tolerability as early as possible to proceed to allo-HSCT. These results suggest that HD-CAG regimen for the second cycle can achieve higher OR rate and should also be considered as an alternative.
During re-induction chemotherapy with intensive salvage regimens, severe adverse effects have been reported to occur. Our study suggested that the dose escalation of aclarubicin on CAG regimen basis did not increase treatment-related mortality. The white blood cell count (WBC) and platelet (PLT) recovery time to more than 0.5 × 109/L and 50 × 109/L was shorter in HD-CAG group than the other 2 groups probably because of G-CSF administration and the lower dose of anti-cancer agents. There were no differences in grade 1-2 and grade 3-4 leucopenia and thrombocytopenia among the 3 groups. These patients had a similar proportion on the incidence of infection among the 3 groups. All patients received blood transfusion support according to blood cell count evaluation. Except for severe complications (which included an early death) in the I/HDAC group, non-hematological toxicity was acceptable among the 3 groups, and routine supportive therapy was able to prevent and resolve complications. Therefore, HD-CAG regimen not only achieved equivalent myelosuppression but also did not result in undue toxicity as compared with I/HDAC and SDAC regimens. Moreover, not all patients are ideal candidates for intensive chemotherapy because of poor performance status or comorbidities or personal wishes. Therefore, lower-intensity therapy is an important treatment option for some patients.
Although older adults (>60 years) have been excluded at the time of enrollment, patients with 50–60 years were much more involved in the HD-CAG group, resulting in a lower allo-HSCT ratio in this cohort. Therefore, higher OR rate and lesser toxicities in this group did not translate into survival advantage. Of course, with the advances in conditioning regimens, supportive care, and multiple choice of donor sources, allo-HSCT can be safely performed in patients with higher age., Therefore, achieving OR remains important for refractory AML patients. Although NCCN guidelines Version 2.2012 for AML recommended HDAC alone or SDAC combination regimen for NR AML patients, our preliminary results suggest that HD-CAG regimen for the second cycle can achieve higher OR rate and should also be considered as an alternative, which is similar to another clinical study.
The mechanisms of priming are probably because of the ability of G-CSF to transition leukemic cells from G0/G1 to S phase, sensitizing the other chemical agents to kill resting leukemia cells., Low-dose Ara-C chiefly induces apoptosis of AML cells, rather than differentiation. Aclarubicin is a less cardiotoxic oligosaccharide anthracycline and it does not only induce leukemic apoptosis by inhibiting DNA replication and RNA synthesis but it also targets multi-drug resistance gene., More importantly, other studies reported that aclarubicin was still effective for daunorubicin-resistant AML patients and hepatoma cells., However, mechanistic studies are required to elucidate this effect of HD-CAG regimen on AML patients.
There are some limitations in this study because it was not randomized, controlled, nor was it large-cohort design, therefore the diversity of post-reinduction treatment may have affected the evaluation of survival effect among the 3 groups. Nonetheless, our results suggested that the major advantage of HD-CAG regimen was in achieving a high OR rate than I/HDAC regimen rather than improving the survival directly.
| » Conclusion|| |
In summary, HD-CAG regimen may improve OR rate than I/HDAC regimens for AML patients refractory to the first cycle of standard “3+7” regimen, particularly for older patients. As this was a pilot study, the efficacy of HD-CAG regimen in comparison to I/HDAC regimens in the NR AML patient population needs to be further confirmed in a larger, well-designed clinical trial in the future.
This study was approved by the Ethics Committee of the First Affiliated Hospital of Soochow University and Haikou Municipal People's Hospital. All patients provided written informed consent, and the study was conducted in line with the Declaration of Helsinki guidelines.
This work was funded by Jiangsu Provincial Special Program of Medical Science (BL2012005) and Jiangsu Province's Key Medical Center (ZX201102).
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| » References|| |
Döhner H, Estey EH, Amadori S, Appelbaum FR, Büchner T, Burnett AK, et al
. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet. Blood 2010;115:453-74.
O'Donnell MR, Abboud CN, Altman J, Appelbaum FR, Arber DA, Attar E, et al
. NCCN Clinical Practice Guidelines Acute myeloid leukemia. J Natl Compr Canc Netw 2012;10:984-1021.
Scheid C, Hermann K, Kremer G, Holsing A, Heck G, Fuchs M, et al
. Randomized, double-blind, controlled study of glycyl-glutamine-dipeptide in the parenteral nutrition of patients with acute leukemia undergoing intensive chemotherapy. Nutrition 2004;20:249-54.
Liu J, Mi Y, Fu M, Yu W, Wang Y, Lin D, et al
. Intensive induction chemotherapy with regimen containing intermediate dose cytarabine in the treatment of de novo
acute myeloid leukemia. Am J Hematol 2009;84:422-7.
Kim DY, Lee JH, Sym SJ, Yun SC, Lee JH, Kim SD, et al
. A prediction model for complete remission upon reinduction for patients with acute myeloid leukemia after failure of anthracycline and cytarabine standard chemotherapy. Ann Hematol 2011;90:1283-91.
Yamada K, Furusawa S, Saito K, Waga K, Koike T, Arimura H, et al
. Concurrent use of granulocyte colony-stimulating factor with low-dose cytosine arabinoside and aclarubicin for previously treated acute myelogenous leukemia: a pilot study. Leukemia 1995;9:10-4.
Wei G, Ni W, Chiao JW, Cai Z, Huang H, Liu D. A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome. J Hematol Oncol 2011;4:46.
Liu L, Zhang Y, Jin Z, Zhang X, Zhao G, Si Y, et al
. Increasing the dose of aclarubicin in low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor (CAG regimen) can safely and effectively treat relapsed or refractory acute myeloid leukemia. Int J Hematol 2014;99:603-8.
Qu Q, Liu L, Zhang Y, Li X, Wu D. Increasing aclarubicin dosage of the conventional CAG (low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor) regimen is more efficacious as a salvage therapy than CAG for relapsed/refractory acute myeloid leukemia. Leuk Res 2015;39:1353-9.
Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, Porwit A, et al
. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 2009;114:937-51.
Who Handbook for Reporting Results of Cancer-Treatment. Neoplasm 1980;27:607-19.
Hao J, Wang L, Wang Y, Liu Z, Gu X, Liu J, et al
. Comparative analysis of decitabine combined with DAG regimen and other regimens in treatment of refractory/relapsed acute myeloid leukemia. Zhonghua Xue Ye Xue Za Zhi 2014;35:481-5.
Roboz GJ. Current treatment of acute myeloid leukemia. Curr Opin Oncol 2012;24:711-9.
Orlowski RJ, Mangan JK, Luger SM. Approach to patients with primary refractory acute myeloid leukemia. Curr Opin Hematol 2015;22:97-107.
Devillier R, Legrand F, Rey J, Castagna L, Fürst S, Granata A, et al
. HLA-Matched Sibling versus Unrelated versus Haploidentical Related Donor Allogeneic Hematopoietic Stem Cell Transplantation for Patients Aged Over 60 Years with Acute Myeloid Leukemia: A Single-Center Donor Comparison. Biol Blood Marrow Transplant 2018;24:1449-54.
Wall SA, Devine S, Vasu S. The who, how and why: Allogeneic transplant for acute myeloid leukemia in patients older than 60 years. Blood Rev 2017;31:362-9.
Zhu HH, Jiang H, Jiang B, Lu J, Jiang Q, Bao L, et al
. Cytarabine, aclarubicin and granulocyte colony-stimulating factor regimen represents an effective and safe salvage regimen for patients with acute myeloid leukemia refractory to first course of induction chemotherapy. Leuk Lymphoma 2013;54:2452-7.
Bai A, Kojima H, Hori M, Nara N, Komeno T, Hasegawa Y, et al
. Priming with G-CSF effectively enhances low-dose Ara-C-induced in vivo
apoptosis in myeloid leukemia cells. Exp Hematol 1999;27:259-65.
Estey EH. Growth factors in acute myeloid leukaemia. Best Pract Res Clin Haematol 2001;14:175-87.
Katagiri T, Miyazawa K, Nishimaki J, Yaguchi M, Kawanishi Y, Ohyashiki K. Combination of granulocyte colony-stimulating factor and low-dose cytosine arabinoside further enhances myeloid differentiation in leukemia cells in vitro
. Leuk Lymphoma 2000;39:173-84.
Minotti G, Menna P, Salvatorelli E, Cairo G, Gianni L. Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity. Pharmacol Rev 2004;56:185-229.
Hajji N, Mateos S, Pastor N, Domínguez I, Cortés F. Induction of genotoxic and cytotoxic damage by aclarubicin, a dual topoisomerase inhibitor. Mutat Res 2005;583:26-35.
Lehne G, De Angelis P, Clausen OP, Rugstad HE. Human hepatoma cells rich in P-glycoprotein are sensitive to aclarubicin and resistant to three other anthracyclines. Br J Cancer 1996;74:1719-29.
Nibu K, Yanai F, Okamura J, Ikuno Y, Tasaka H, Matsuzaki A, et al
. An effective salvage regimen with aclarubicin for daunorubicin-resistant acute non-lymphocytic leukemia in children. Pediatr Hematol Oncol 1995;12:251-8.
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