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A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome
Journal of Hematology & Oncology volume 4, Article number: 46 (2011)
The regimen of cytarabine, aclarubicin and G-CSF (CAG) has been widely used in China and Japan for treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). We searched literature on CAG between 1995 and 2010 and performed a meta-analysis to determine its overall efficacy using a random-effects or fixed-effects model. Thirty five trials with a total of 1029 AML (n = 814) and MDS (n = 215) patients were included for analysis. The CR rate of AML (57.9%) was significantly higher than that of MDS (45.7%) (p < 0.01). No difference in CR was noted between the new (56.7%) and relapsed/refractory AML (60.1%) (p > 0.05). The CR rate was also significantly higher in patients with favorable (64.5%) and intermediate (69.6%) karyotypes than those with unfavorable one (29.5%) (p < 0.05). Remarkably, the CR rate of CAG was significantly higher than those of non-CAG regimens (odds ratio 2.43). CAG regimen was well tolerated, with cardiotoxicity in 2.3% and early death in 5.2% of the cases. In conclusion, CAG regimen was an effective and safe regimen for the treatment of AML, and may be more effective than non-CAG regimens. Randomized controlled trials are strongly recommended to evaluate its efficacy and safety in comparison with the current standard treatment.
Intensive chemotherapy can achieve complete remission (CR) in 60% - 80% of patients with newly diagnosed de novo acute myeloid leukemia (AML) [1, 2]. However, current therapy is still unsatisfactory in patients with high-risk AML including elderly, relapsed, refractory, and secondary AML. Intensive chemotherapy is generally unsatisfactory in these patients because of drug resistance, poor performance status (PS), dysfunction of multiple organs, and high treatment-related toxicities, leading to high early death (ED) rate [3–6]. Novel agents and regimens are being developed for this group of patients [2, 7–10].
Aclarubicin is an oligosaccharide anthracycline, and an antineoplastic antibiotic. It can intercalate into DNA and interact with topoisomerase I and II, thereby inhibiting DNA replication and DNA repair . This agent is less cardiotoxic than doxorubicin and daunorubicin [12, 13]. In 1995, a Japanese group reported a new chemotherapy regimen for AML treatment, which integrated granulocyte colony-stimulating factor (G-CSF) priming into the combination of low-dose cytarabine (Ara-C) and aclarubicin (CAG regimen) . The CAG regimen consists of low-dose Ara-C 10 mg/m2, SQ Q12 hr on days 1-14, aclarubicin 7 mg/m2, QD on days 1-8, or 14 mg/m2, IV QD on days 1-4, and G-CSF 200 μg/m2, SQ QD on days 1-14. The rationale for the regimen includes: (1) G-CSF priming has been found to preferentially potentiate Ara-C and anthracycline- mediated cytotoxicity on AML cells and AML progenitor cells (CFU-AML), presumably by enhancing G0 resting AML cells into the cell cycle ; (2) prolonged exposure to low-dose Ara-C and G-CSF can lead to preferential killing of CFU-AML ; (3) Aclarubicin is effective regardless of multi-drug resistance gene status ; (4) CAG combination may inhibit the self-renewal capacity of CFU-AML and leukemia stem cells . Since then, CAG regimen has been used to treat AML and myelodysplastic syndrome (MDS) patients widely, particularly for high-risk and elderly patients, in China and Japan. However, the overall efficacy and safety of CAG regimen have not been adequately evaluated. All published studies on CAG were small phase II studies with significant variation in clinical outcomes. In this study, we performed a systematic review and meta-analysis to assess the overall treatment efficacy and the adverse events of the CAG regimen.
Materials and methods
The databases of PubMed, Wanfang Data, as well as American Society of Hematology (ASH) and American Society of Clinical Oncology (ASCO) annual meeting abstracts were searched for articles published in English, Chinese and Japanese languages between January 1995 and December 2010. Eligible studies were relevant clinical trials on AML and MDS patients treated with CAG regimen. Key words used were CAG, chemotherapy, leukemia, and MDS. An independent search using the citation database Wanfang Data (http://www.wanfangdata.com) was also performed to identify those publications in Chinese only.
The publications identified were carefully screened. Preclinical studies, case reports and reviews were excluded. Several reports had duplicate or overlapping information. Only the latest updated reports were included for meta-analysis. For two studies by Qian's group [19, 20], it was impossible to decipher whether duplicate or overlapping information was used. These were treated as individual studies. Efforts also were made to contact the Chinese investigators to clarify study issues. We also contacted Japanese investigators to obtain original publications in Japanese with English abstracts.
We extracted details on study characteristics, patient characteristics, treatment information, results and follow-up from the selected trials. Two investigators reviewed the data independently (GW and DL). The primary end point of the meta-analysis was CR rate. AML CR was defined using the criteria developed by an International Working Group . The criteria for refractory and relapsed AML were described previously . The criteria for karyotype classification have evolved over the past decades [4, 23, 24]. In general, the 35 studies chosen for final analysis followed the standard definitions described above. CR rates and side effects were carefully reviewed and compiled. Two major side effects, cardiotoxicity and early death (ED), were chosen for further analysis since these two toxicities are generally more objective. In studies which did not clearly define the criteria of cardiotoxicity, the toxicity was counted as being present when a study reported mortality cases due to cardiac causes. There were different criteria for ED definition among the studies. All deaths of any cause within 8 weeks of induction therapy were counted as ED in this meta-analysis since most of the early death reports in this series were within 8 weeks of induction therapy. This would also reduce the chance of under-reporting the toxicity. Standard age definitions were used, i.e. young AML: age < = 60; Elderly AML: age >60.
All statistical analyses were performed using version 2 of the Comprehensive MetaAnalysis program (Biostat, Englewood, NJ, USA). The CR rates of patients treated with CAG regimen were directly extracted from individual studies. For subgroup analysis of patients with newly diagnosed, refractory/relapsed AML, and MDS or AML transformed from MDS (MDS/t-AML) patients, numbers of patients in CR were extracted from individual studies and CR rates were recalculated from the derived data. For studies with a control group, the odds ratio (OR) of CR rates was also calculated. For the meta-analysis, both fixed-effects and random-effects models were considered. For each meta-analysis, the Cochrane's Q statistic was first calculated to assess the heterogeneity of the included studies. For p values less than 0.1, the assumption of homogeneity was deemed invalid, and the random-effects model was used only after substantial efforts were made to explore the possible reasons for the heterogeneity. Otherwise, data were assessed using both fixed-effects and random-effects models. We used the Begg and Egger tests to evaluate the presence of publication bias regarding the primary end point CR rates. A two-tailed p value of less than 0.05 was deemed statistically significant. All the statistical analyses were done by GW and DL.
Selection of studies
Using the key words, our search yielded a total of 135 studies on CAG. Fifty seven studies were irrelevant to CAG regimen trials, and were excluded. Another 32 studies were eliminated due to inadequate information, duplicate and/or overlap reporting. Nine case reports and 2 studies focus on other kinds of leukemia were also excluded. A total of 35 clinical studies were eligible for inclusion and were used for final meta-analysis (Figure 1).
Characteristics of studies included in the meta-analysis
Thirty five trials were included in the present analysis, with a total of 1029 patients accrued. Characteristics of the 35 trials are listed in Tables 1 and 2. Twenty three of the studies were on AML. Six of the studies focused on MDS. The rest 6 studies enrolled both AML and MDS patients. A total of 814 AML patients were accrued in 29 studies. Among the 814 AML patients, 327 patients had newly diagnosed AML, 370 patients were relapsed/refractory (R/R) AML. AML status of 117 patients was not specified in 7 studies [19, 20, 25–29]. The age varied widely, ranging from 15 to 88 years old. Two studies did not indicate the age range (Table 1). Unfortunately, median age was not specified in most studies. Among the 814 patients, 367 were elderly AML patients (45.1%). Cytogenetic characteristics from 203 AML patients were reported in 6 studies. These patients were grouped into 3 categories according to the karyotypes: favorable, intermediate and unfavorable. CAG regimen was compared to historical controls using non-CAG induction regimens in 7 studies with 327 patients. The number of CAG cycles was clearly reported in 17 studies involving 397 patients, of whom 144 (36.2%) were induced twice with CAG.
No evidence of publication bias was detected for the primary end point, CR, of this study by either the Begg or Egger test (Begg test, p = 0.35; Egger test, p = 0.15).
Efficacy of CAG regimen for all AML and high-risk MDS/transformed AML
The heterogeneity test of CR event rates from the 35 studies revealed Q 59.431, p 0.025, I2 32.695, indicating the CR event rates were highly variable. Therefore, the CR event rates were calculated using the random-effects model (Figure 2). The overall CR rate for the 1029 patients was 53.7% (95% CI, 49.7%-57.6%). Data available from 29 trials with 814 AML patients showed that the CR rate was 57.9% (95% CI, 53.0%-62.7%). As for the 215 patients with MDS and transformed AML (MDS/t-AML) from 12 trials, the CR rate was 45.7% (95% CI, 39.0%-52.4%) (Figure 2).
We also compared CAG in AML versus MDS. The higher CR rate in AML (57.9%) than in MDS (45.7%) was statistically significant (p = 0.004) (Figure 2). This is in agreement with the past observations that AML responds better to chemotherapy in general than MDS.
Among AML patients, the median OS was 15 months (range 9-28 months). The number of CAG cycles was specified in 17 studies involving 397 patients, of whom 144 (36.2%) were induced twice with CAG. Of the patients who received one cycle, 46.60% (185/397) went into CR, another 8.31% (33/397) of the patients achieved CR after re-induction with CAG.
Efficacy of CAG regimen for newly diagnosed vs relapsed/refractory AML
There were a total of 327 new AML patients from 14 studies, and 370 patients with relapsed/refractory (R/R) AML from 15 studies. Four of these studies enrolled both new and R/R AML (Table 3 and Figure 3). These four studies were separated into new and R/R AML groups for meta-analysis. Another seven studies did not specify AML status of the rest 117 patients. These 117 patients were therefore excluded for this comparison (Table 3). The heterogeneity test of CR event rates of these studies revealed Q 48.608, p 0.009, I2 42.396, indicating the CR event rates were highly variable. Therefore, the CR event rates were calculated using the random-effects model (Figure 3). The CR rate for the newly diagnosed AML patients was 56.7% (95% CI, 51.1%-62.0%). The CR rate of the 370 R/R AML patients was 60.1% (95% CI, 50.5%-68.9%) (Figure 3). Interestingly, no significant difference in CR rate was noted between the newly diagnosed and R/R AML patients (p = 0.539) (Table 3 and Figure 3), suggesting that this novel regimen may overcome AML resistance.
CR rates in AML patients according to karyotypes
Cytogenetic characteristics from 203 AML patients were reported in 6 studies (Table 4). The heterogeneity test of CR event rates revealed Q 35.323, p 0.004, I2 54.707, indicating the CR event rates were highly variable. Therefore, the CR event rates were calculated using the random-effects model (Figure 4). The CR rates were 64.5% (95% CI, 38.8%-83.9%), 69.6% (95% CI, 60.4%-77.5%) and 29.5% (95% CI, 19.7%-41.8%) in favorable, intermediate and unfavorable groups, respectively. Statistical difference of the CR rates was noted between the favorable and unfavorable groups (p = 0.018) as well as between the intermediate and unfavorable groups (p < 0.001). No significant difference was present between the favorable and intermediate groups (p = 0.705) (Figure 4).
CAG vs non-CAG regimens for AML induction
Using historical controls, CAG regimen was compared with non-CAG regimens for AML induction in 7 trials. 165 patients were treated with CAG, 162 were induced with non-CAG regimens (the regimen details are provided in the Table 5). The heterogeneity test of CR event rates from the 7 studies revealed Q 3.631, p 0.726, I2 <0.001, indicating that there was no significant variation among the 7 studies. Therefore, the CR event rates were calculated using the fixed-effects model (Figure 5). Surprisingly, the CR rate of CAG was significantly higher than those of other regimens, with an odds ratio of 2.43 (95% CI, 1.52-3.88) (Figure 5).
Cardiotoxicity and early death rate of CAG
The toxicity of CAG in all reports was generally mild. Cardiotoxicity data were reported in 33 studies with 953 patients, and ED was reported in 34 studies with 1021 patients. Cardiotoxicity rate was 2.3% (95% CI, 1.5%-3.6%) (actuarial rate 0.42%, 4/953) (Tables 1 and 2, Figure 6). ED rate was 5.2% (95% CI, 3.5%-7.6%) (actuarial rate 4.31%, 44/1021) (Tables 1 and 2, Figure 7). Among AML patients, the cardiotoxicity rate was 2.4% (95% CI, 1.5%-4.0%) (actuarial rate 0.41%, 3/738), and ED rate was 5.9% (95% CI, 3.9%-8.8%) (actuarial rate 5.09%, 41/806). Most of the death was caused by severe infection, cardiopulmonary dysfunction or cerebral hemorrhage.
CAG regimen was originally designed in Japan for the treatment of relapsed AML patients in 1995. It quickly became popularized in China for the treatment of high-risk AML and MDS patients due to relatively mild toxicity. Most of the studies were single-center non-randomized trials with small sample size. CAG has not been systematically compared with other induction regimens. In this meta-analysis, 1029 patients with AML and MDS were treated with CAG regimen. Two findings on CR rate for AML are quite intriguing. Number one, there was no significant differences in CR rates between new (56.7%) and relapsed/refractory (60.1%) AML. This is surprising since the CR rate is generally lower for R/R than new AML. One possibility is that this novel CAG regimen can overcome the drug resistance of the R/R AML clone and lead to high CR rate. Alternatively, it may be that the first-line induction therapy was substandard in these patients from diverse institutions with different supportive care standards. Therefore, the relapsed and refractory AML was still sensitive to alternative chemotherapy. The CR rate of CAG (56.7%) for new AML appears to be slightly lower than the CR rate of standard "3+7" regimen (daunorubicin 45 mg/m2 + Ara-C 100 mg-200 mg/m2) (57%-65%) [5, 7, 30, 31] (Table 6). However, there have been no randomized studies, it is therefore not clear whether CAG is as effective as "3+7".
The second finding is that, as frontline AML regimen, CAG induced higher CR rate in AML than non-CAG regimens (p < 0.001, odds ratio 2.43 favoring CAG). The non-CAG regimens included anthracyclines plus Ara-C in 5 studies (AA regimens), and homoharringtonine plus Ara-C (HA regimen) in two other studies. HA is only used in China . When CAG was compared with the 5 AA regimens, CAG remains superior to the AA regimens in CR rate (p < 0.001, odds ratio 2.73, 95% CI 1.61-4.64). However, the studies were not randomized, and the comparisons in those studies were made with historical controls. It is therefore worthwhile to compare CAG regimen with standard anthracycline plus Ara-C in a prospective randomized study.
In this meta-analysis, the CR rate of CAG regimen for high-risk MDS/t-AML patients was 45.7% (95% CI, 39.0%-52.4%). Aza-001 trial, a prospective randomized study, compared azacitidine with conventional care regimen (best supportive care, low dose Ara-C, or intensive chemotherapy "3+7") in higher-risk MDS patients . The CR rate was 17% and 36% in the azacitidine group and "3+7" group, respectively. Yet azacitidine led to prolonged overall survival in the high-risk MDS patients. CAG gained popularity in China and Japan in the past decade because, based solely on small phase II studies, it is widely believed to be a milder regimen than "3+7" for high-risk and elderly AML and MDS patients. It is therefore valuable to perform a prospective randomized trial in high-risk elderly MDS patients to compare CAG with "3+7" for their effects on overall survival.
There have not been many reports focusing on toxicities of AML inductions. In the report of "3+7" regimen on 326 new AML patients from the Cancer and Leukemia Group B 8321 study, the overall induction mortality was 15% . Data from the Swedish Acute Leukemia Registry from all unselected 2767 AML patients found an overall ED (30 days from diagnosis) rate of 19% (range 4-40% according to age) . The ED rate was 10% for intensive chemotherapy group, and 34% for palliative group. The data clearly supported chemotherapy for all age groups. In a phase III randomized study comparing high with standard dose daunorubicin in 657 young (age ≤ 60) AML patients , induction mortality was 4.5% in the standard group, 5.5% in the high dose group (p = 0.60). This study reported cardiac toxicity of 7.2% in the standard dose group with no reduction in ejection fraction. In a separate phase III randomized study comparing high with standard dose daunorubicin in 813 elderly (age ≥ 60) AML patients , 30-day mortality was found to be 12% in the standard group, 11% in the high dose group (p = 0.59). Cardiac toxicity was not specified in this study. Kantarjian's group reported their 15 years' experience of induction chemotherapy on 510 high-risk MDS patients (median age 63) . The overall ED (death within 7 weeks of induction) rate was 17% (topotecan-Ara-C 6%, anthracycline-Ara-C 17%, fludarabine-Ara-C 23%). In our analysis, it was difficult to quantify toxicities from so many small phase II studies, which were from diverse institutions in China and Japan with different supportive care standards. We therefore chose two relatively objective parameters, cardiotoxicity and ED rate. In this analysis, cardiotoxicity was 2.3% and ED was 5.2% among all AML and MDS patients. For new AML patients, the ED rate was 9.0%, whereas the ED for MDS was only 4.8% (Table 6). Taken together all these experiences of induction efficacy and toxicities (Table 6), it appears that CAG regimen was effective and well tolerated.
This study has severe limitations. First of all, this study is based on 35 trials which were conducted in China and Japan, where significant variations in supportive care may have existed. In addition, the studies were between 1995 and 2010. Newer molecular prognostic markers, such as FLT3 and NPM1, were not routinely tested in most of the studies. The standard of supportive care for AML has changed dramatically over the decade. The toxicity data from this analysis may therefore overestimate the adverse events of the regimens under current health care system. Majority of the studies were small (only 9 of the 35 studies had 50 or more subjects). Although all the studies used similar CAG regimens, the dosage of aclarubicin was variable. Due to the small sample sizes and ambiguity in reporting the AML status in the 7 studies, it was difficult to ascertain whether the variation of the aclarubicin dosage could have played any role in the outcomes among the different groups of AML (new vs R/R) and MDS/t-AML. There was no randomized study among the 35 reports. CAG was compared with non-CAG regimens from historical controls in the 7 reports. The non-CAG regimens also varied. Two of the seven reports did not include anthracyclines. It is therefore possible that the superiority of CAG over non-CAG regimen may have been overestimated, even when the more stringent fixed-effects model was used. Estimation of CR event rates using random-effects model may minimize the inherent variances. Finally, CAG regimen is used exclusively in China and Japan. It is not clear whether similar outcome is reproducible in the Western countries.
In conclusion, CAG regimen was effective and safe for the treatment of AML and MDS patients. Its activity may vary among these patients with significantly higher CR rates observed in AML than MDS. It was as active in new AML as in relapsed and refractory AML. CAG regimen may be more effective than non-CAG regimen with the CR rate of CAG regimen significantly higher than those of non-CAG induction regimens in AML patients. This regimen was well tolerated with low cardiotoxicity and ED rate. We strongly recommend that CAG regimen be compared with standard anthracycline plus Ara-C in a prospective randomized study, particularly in high-risk and elderly AML and MDS patients.
Freireich EJ: Four decades of therapy for AML. Leukemia. 1998, 12 (Suppl 1): S54-56.
Zhu X, Ma Y, Liu D: Novel agents and regimens for acute myeloid leukemia: 2009 ASH annual meeting highlights. J Hematol Oncol. 2010, 3: 17-10.1186/1756-8722-3-17.
Estey EH: Treatment of relapsed and refractory acute myelogenous leukemia. Leukemia. 2000, 14 (3): 476-479. 10.1038/sj.leu.2401568.
Gregory TK, Wald D, Chen Y, Vermaat JM, Xiong Y, Tse W: Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics. J Hematol Oncol. 2009, 2: 23-10.1186/1756-8722-2-23.
Juliusson G, Antunovic P, Derolf A, Lehmann S, Mollgard L, Stockelberg D, Tidefelt U, Wahlin A, Hoglund M: Age and acute myeloid leukemia: real world data on decision to treat and outcomes from the Swedish Acute Leukemia Registry. Blood. 2009, 113 (18): 4179-4187. 10.1182/blood-2008-07-172007.
Pidala J, Kim J, Anasetti C, Kharfan-Dabaja MA, Nishihori T, Field T, Perkins J, Perez L, Fernandez HF: Pharmacokinetic targeting of intravenous busulfan reduces conditioning regimen related toxicity following allogeneic hematopoietic cell transplantation for acute myelogenous leukemia. J Hematol Oncol. 2010, 3: 36-10.1186/1756-8722-3-36.
Fernandez HF, Sun Z, Yao X, Litzow MR, Luger SM, Paietta EM, Racevskis J, Dewald GW, Ketterling RP, Bennett JM: Anthracycline dose intensification in acute myeloid leukemia. N Engl J Med. 2009, 361 (13): 1249-1259. 10.1056/NEJMoa0904544.
Fremin C, Meloche S: From basic research to clinical development of MEK1/2 inhibitors for cancer therapy. J Hematol Oncol. 2010, 3: 8-10.1186/1756-8722-3-8.
Jiang S, Ma X, Huang Y, Xu Y, Zheng R, Chiao J-W: Reactivating aberrantly hypermethylated p15 gene in leukemic T cells by a phenylhexyl isothiocyanate mediated inter-active mechanism on DNA and chromatin. Journal of Hematology & Oncology. 2010, 3 (1): 48-10.1186/1756-8722-3-48.
Raza A, Galili N, Callander N, Ochoa L, Piro L, Emanuel P, Williams S, Burris H, Faderl S, Estrov Z: Phase 1-2a multicenter dose-escalation study of ezatiostat hydrochloride liposomes for injection (Telintra(R), TLK199), a novel glutathione analog prodrug in patients with myelodysplastic syndrome. Journal of Hematology & Oncology. 2009, 2 (1): 20-10.1186/1756-8722-2-20.
Hajji N, Mateos S, Pastor N, Dominguez I, Cortes F: Induction of genotoxic and cytotoxic damage by aclarubicin, a dual topoisomerase inhibitor. Mutat Res. 2005, 583 (1): 26-35.
Warrell RP: Aclacinomycin A: clinical development of a novel anthracycline antibiotic in the haematological cancers. Drugs Exp Clin Res. 1986, 12 (1-3): 275-282.
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 (2): 185-229. 10.1124/pr.56.2.6.
Yamada K, Furusawa S, Saito K, Waga K, Koike T, Arimura H, Aoyagi A, Yamato H, Sakuma H, Tsunogake S: 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 (1): 10-14.
Tafuri A, Andreeff M: Kinetic rationale for cytokine-induced recruitment of myeloblastic leukemia followed by cycle-specific chemotherapy in vitro. Leukemia. 1990, 4 (12): 826-834.
Van Der Lely N, De Witte T, Muus P, Raymakers R, Preijers F, Haanen C: Prolonged exposure to cytosine arabinoside in the presence of hematopoietic growth factors preferentially kills leukemic versus normal clonogenic cells. Exp Hematol. 1991, 19 (4): 267-272.
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 (11): 1719-1729. 10.1038/bjc.1996.621.
Ferrero D, Carlesso N, Pregno P, Gallo E, Pileri A: Self-renewal inhibition of acute myeloid leukemia clonogenic cells by biological inducers of differentiation. Leukemia. 1992, 6 (2): 100-106.
Qian S, Li J, Wu H, Lu H, Zhang X, Ren Z: Low-dose cytorabine and aclarubicin in combination with G-CSF for patients with acute myeloid leukemia. Acta univ medi Nanjing (Natu Sci). 2005, 25 (2): 116-117.
Qian SX, Li JY, Tian T, Shen YF, Jiang YQ, Lu H, Wu HX, Zhang SJ, Xu W: Effect of low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor priming (CAG regimen) on the outcome of elderly patients with acute myeloid leukemia. Leuk Res. 2007, 31 (10): 1383-1388. 10.1016/j.leukres.2007.02.009.
Cheson BD, Bennett JM, Kopecky KJ, Buchner T, Willman CL, Estey EH, Schiffer CA, Doehner H, Tallman MS, Lister TA: 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 Clin Oncol. 2003, 21 (24): 4642-4649. 10.1200/JCO.2003.04.036.
Schiller GJ: Treatment of resistant disease. Leukemia. 1998, S20-24. 12 Suppl 1
Schoch C, Kern W, Schnittger S, Hiddemann W, Haferlach T: Karyotype is an independent prognostic parameter in therapy-related acute myeloid leukemia (t-AML): an analysis of 93 patients with t-AML in comparison to 1091 patients with de novo AML. Leukemia. 2004, 18 (1): 120-125. 10.1038/sj.leu.2403187.
Slovak ML, Kopecky KJ, Cassileth PA, Harrington DH, Theil KS, Mohamed A, Paietta E, Willman CL, Head DR, Rowe JM: Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood. 2000, 96 (13): 4075-4083.
Huang M, Zhou J, Zhang D, Sun H, Deng J, liu W: Clinical study of CAG regimen in acute myeloid leukemia. J Clin Hematol. 2005, 18 (5): 266-267.
Li JM, Shen Y, Wu DP, Liang H, Jin J, Chen FY, Song YP, Song EY, Qiu XF, Hou M: Aclarubicin and low-dose Cytosine arabinoside in combination with granulocyte colony-stimulating factor in treating acute myeloid leukemia patients with relapsed or refractory disease and myelodysplastic syndrome: a multicenter study of 112 Chinese patients. Int J Hematol. 2005, 82 (1): 48-54. 10.1532/IJH97.A10424.
Liu W, Li F, Guo Y, Song H, Huang S, Zuo J: Clinical efficacy of CAG regimen in relapsed and refractory AML patients. Chin J Coal Indust Med. 2006, 9 (4): 362-363.
Ma H, Cheng J, Liu B: Clinical study of cytarabine, aclarubicin and G-CSF regimen in acute myelogenous leukemia and the ralation with karyotypes. J Lanzhou Univ (Med Sci). 2010, 36 (3): 61-63.
Su G, Wang X, Huang D, Dai Y, Yao J: Treatment of elderly refractory AML with CAG regimen. J Leuk Lymph. 2007, 16 (1): 57-58.
Dillman RO, Davis RB, Green MR, Weiss RB, Gottlieb AJ, Caplan S, Kopel S, Preisler H, McIntyre OR, Schiffer C: A comparative study of two different doses of cytarabine for acute myeloid leukemia: a phase III trial of Cancer and Leukemia Group B. Blood. 1991, 78 (10): 2520-2526.
Lowenberg B, Ossenkoppele GJ, van Putten W, Schouten HC, Graux C, Ferrant A, Sonneveld P, Maertens J, Jongen-Lavrencic M, von Lilienfeld-Toal M: High-dose daunorubicin in older patients with acute myeloid leukemia. N Engl J Med. 2009, 361 (13): 1235-1248. 10.1056/NEJMoa0901409.
Wang J, Lu S, Yang J, Song X, Chen L, Huang C, Hou J, Zhang W: A homoharringtonine-based induction regimen for the treatment of elderly patients with acute myeloid leukemia: a single center experience from China. J Hematol Oncol. 2009, 2: 32-10.1186/1756-8722-2-32.
Fenaux P, Mufti GJ, Hellstrom-Lindberg E, Santini V, Finelli C, Giagounidis A, Schoch R, Gattermann N, Sanz G, List A: Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: a randomised, open-label, phase III study. Lancet Oncol. 2009, 10 (3): 223-232. 10.1016/S1470-2045(09)70003-8.
Kantarjian H, Beran M, Cortes J, O'Brien S, Giles F, Pierce S, Shan J, Plunkett W, Keating M, Estey E: Long-term follow-up results of the combination of topotecan and cytarabine and other intensive chemotherapy regimens in myelodysplastic syndrome. Cancer. 2006, 106 (5): 1099-1109. 10.1002/cncr.21699.
Saito K, Furusawa S, Yamada K, Waga K, Aoyagi A, Koike T, Arimura H, Noguchi M, Yamato H, Sakuma H: Comparison of low-dose cytosine arabinoside and aclarubicin in combination with granulocyte colony-stimulating factor to intermediate-dose cytosine arabinoside and mitoxantrone with or without etoposide in the treatment of relapsed acute myeloid leukemia. Rinsho Ketsueki. 1995, 36 (3): 165-174.
Saito K: Low-dose cytosine arabinoside and aclarubicin in combination with granulocyte colony-stimulating factor for the treatment of relapsed acute myeloid leukemia. Rinsho Ketsueki. 1996, 37 (8): 651-653.
Tabata M, Yoshida M, Izumi T, Kawano C, Kuribara R, Toshima M, Omine K, Takatoku M, Uchida M, Kirito K: Retrospective analysis of elderly patients > or = 60 years of age with acute leukemia. Rinsho Ketsueki. 1998, 39 (3): 176-184.
Saito K, Nakamura Y, Aoyagi M, Waga K, Yamamoto K, Aoyagi A, Inoue F, Arai Y, Tadokoro J, Handa T: Low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor (CAG regimen) for previously treated patients with relapsed or primary resistant acute myelogenous leukemia (AML) and previously untreated elderly patients with AML, secondary AML, and refractory anemia with excess blasts in transformation. Int J Hematol. 2000, 71 (3): 238-244.
Hirayama Y, Sakamaki S, Takayanagi N, Tsuji Y, Sagawa T, Chiba H, Matsunaga T, Niitsu Y: Chemotherapy with ubenimex corresponding to patient age and organ disorder for 18 cases of acute myelogeneous leukemia in elderly patients--effects, complications and long-term survival. Gan To Kagaku Ryoho. 2003, 30 (8): 1113-1118.
Kong L: Clinical efficacy of CAG regimen in AML. J Clin Hematol. 2005, 18 (6): 360-
Yang R, Li C, Liu H, Du C: Clinical efficacy of CAG regimen in elderly AML. J Leuk Lymph. 2005, 14 (4): 238-239.
Xie X: Treatment of elderly AML with CAG regimen. J Leuk Lymph. 2006, 15 (2): 132-133.
Wang S, Liang L, Ju S: Clinical efficacy of CAG regimen in relapsed and refractory AML patients. Hainan Med J. 2006, 17 (12): 89-90.
Wu G, Bian X, Wei C, Wang Z, Zhang X: The treatment of elderly AML with CAG regimen. Chin Clin oncol. 2007, 12 (2): 143-144.
Guo L, Zhao X, Li W: Treatment of 8 cases of relaped APL with CAG regimen. J Leuk Lymph. 2007, 16 (1): 65-66.
Chen YJ, Zhang LQ, Li XL, Zhao XL, Wu DS, Shu YG, Chen FP: Therapeutic effect of priming induction regimen of CAG for newly diagnosed acute myeloid leukemia in elderly patients. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2008, 33 (3): 245-251.
Sang Y, Zhao W, Meng Q, Xia J: Clinical efficacy of CAG regimen compared with other regimens in elderly AML patients. J Leuk Lymph. 2008, 17 (4): 297-299.
Bian J, Ma J, DENG X, Chen J, Chen L: Therapeutic effect of CAG regimen on patients with recurrent acute myelocytic leukemia. J Clin Hematol. 2008, 21 (7): 345-347.
Chai JY, Zheng WQ, Wei N: Clinical research of modified CAG regimen for the treatment of relapsed acute myeloid leukemia. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2009, 17 (4): 1061-1063.
Zhu B, Qian S, Hong M, Lu H, Wu H, Zhang S, Chou H, Xu W, lI J: CAG priming in 50 patients with relapsed acute myeloid leukemia. J Clin Exp Hematol. 2009, 17 (3): 760-764.
Ni B, Chen F, Han J, Zhong H, Zhong L, Huang H, Shen L, Xiao F: Outcome and survival analysis of patient with AML and high risk MDS treated by CAG regimen. J Shanghai Jiaotong Univ (Med Sci). 2009, 29 (11): 1355-1358.
Feng Y, Huang M, Zheng D: Clinical efficacy of HA and CAG regimen on elderly patients with acute non-lymphocytic leukemia. J Bengbu Med Col. 2010, 35 (6): 2-
Li S, Pei R, Ma J, Zhang P, Liu X, Du X, Chen D, Sha K, Chen L, Cao J: Efficacy of CAG and HAG regimen in refractory and relapsed AML patients. Zhejiang Med J. 2010, 32 (2): 275-276.
Liang H, Zhao H: Clinical effect of CAG regimen on patients with AML and MDS. J Leuk Lymph. 2010, 19 (10): 607-609.
Suzushima H, Wada N, Yamasaki H, Eto K, Shimomura T, Kugimiya MH, Horikawa K, Nishimura S, Tsuda H, Mitsuya H: Low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor for elderly patients with previously untreated acute myeloid leukemia. Leuk Res. 2010, 34 (5): 610-614. 10.1016/j.leukres.2009.08.010.
Sui X, Zhou H, Liu X, Li Y, Wang X, Xu H: Treatment outcome of CAG regimen for the intermediate and high risk myelodysplastic syndrome. Chin J Cancer Prev Treat. 2008, 15 (21): 1666-1668.
Jin T, Zhao M, Chen Y, Chen Y, Li L: Treatment of MDS with CAG regimen. J Wenzhou Med Col. 2008, 38 (4): 383-
Deng C, Wen G, Ma Y, Lin Y: The study of erythopietin receptor and researched 4 different plans for curing MDS. Sichuan Med J. 2008, 29 (9): 1126-1128.
Su JY, Chang CK, Zhang X, Zhou LY, Song LQ, Xu L, Wu LY, He Q, Li X: Efficacy of induction chemotherapy for patients with high-risk myelodysplastic syndrome (MDS) or MDS-transformed acute myeloid leukemia with CHG regimen and its comparison with regimen GAG and HA. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2009, 17 (2): 459-463.
Li Z, Guo C, Zhang H, Liu Y: Efficacy of CAG regimen in MDS patients. J Leuk Lymph. 2010, 19 (10): 630-631.
Zhu Y, He Y, Chen S: Curative effect of low dose cytarabine and aclarubin in combination with granulocyte colony-stimulating factor priming (CAG regimen) on patients with the intermediate and high-risk myelodysplastic syndrome. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010, 35 (4): 370-373.
Chen H, Qian S, Li J, Sun M, Wu H, Zhang S: Clinical efficacy of CAG regimen in MDS patients. Chin J Intern Med. 2010, 49 (8): 703-704.
We are deeply indebted to Dr. Shenhong Wu, Associate Professor of Medicine from SUNY Stonybrook Health Sciences Center for guidance on the meta-analysis and critical review of the manuscript. We are also grateful to Dr. Norio Asou from Kumamoto University of Japan for getting us three original articles in Japanese. Dr. Wei is a CAHON scholar (http://CAHON.org) and was supported in part by the Research Fund from the Doctoral Program of Higher Education of China (No.J20070747) and the National Natural Science Foundation of China (No. 91029740). This study was also supported in part by NYMC Blood Disease Fund (DL).
The authors declare that they have no competing interests.
GW and DL participated in concept design, data collection and analysis, drafting and critically revising the manuscript. All authors are involved in reviewing and revising the manuscript. All authors have read and approved the final manuscript.
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Wei, G., Ni, W., Chiao, J. et al. 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 4, 46 (2011). https://doi.org/10.1186/1756-8722-4-46
- acute myeloid leukemia
- myelodysplastic syndrome