Korean J Hematol 2010; 45(3):
Published online September 30, 2010
https://doi.org/10.5045/kjh.2010.45.3.177
© The Korean Society of Hematology
1Department of Laboratory Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
2Department of Internal Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
Correspondence to : Correspondence to Hyun-Sook Chi, M.D., Ph.D. Department of Laboratory Medicine, Asan Medical Center, 86 Asanbyeongwon-gil, Songpa-gu, Seoul 138-736, Korea. Tel: +82-2-3010-4502, Fax: +82-2-478-0884, hschi@amc.seoul.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Therapy-related myeloid neoplasm (t-MN) is a distinct class of acute myeloid leukemia (AML) in the World Health Organization (WHO) classification. Both AML and acute lymphoblastic leukemia (ALL) may develop after treatment for primary cancer. Topoisomerase inhibitors are commonly used to treat breast cancer patients and are well-known for their effect on leukemogenesis of therapy-related acute leukemias (t-AL).
We retrospectively evaluated bone marrow test results, chromosomal findings, and clinical characteristics of 12 patients who received topoisomerase inhibitors for breast cancer treatment and later developed acute leukemia.
Fourteen patients (0.2%) developed t-AL after treatment for breast cancer. Topoisomerase inhibitors were administered to 12 patients. Among them, 9 patients (75%, 9/12) were diagnosed with therapy-related AML (t-AML) and 3 patients (25%, 3/12) with therapy-related ALL (t-ALL). Eight patients (67%, 8/12) showed translocation involving 11q23 and 3 different partner genes, 19p13.1 (37.5%, 3/8), 9p22 (37.5%, 3/8), and 4q21 (25%, 2/8). The median interval between completion of chemotherapy for breast cancer and occurrence of t-AL was 25 months. Patients with 11q23 translocation showed markedly poorer event-free survival than the group without involvement of 11q23.
The incidence rate of t-AL after treatment for breast cancer was 0.2% in a tertiary hospital in Korea. Translocation involving the
Keywords Therapy-related acute myeloid leukemia, Breast cancer, Topoisomerase inhibitors, 11q23
Therapy-related acute leukemia (t-AL) is the most severe complication that may occur after treatment for primary cancer. It is diagnosed on the basis of histories of treatment and molecular abnormalities, and develops after chemotherapy, radiation, or immunosuppressive agents performed for the management of the primary cancer [1]. The World Health Organization (WHO) recognizes therapy-related myeloid neoplasm (t-MN) as a distinct subtype of acute myeloid leukemia (AML), although acute lymphoblastic leukemia (ALL) may also arise [2]. Topoisomerase inhibitors and alkylating agents are 2 well-known antineoplastic agents that cause t-AL [3].
The incidence rate of t-AL among patients treated for breast cancer has been reported to be 0.2-0.5% [4]. Breast cancer is the second most common cancer in Korean women, and such serious side effects are a matter of concern [5]. Topoisomerase inhibitors are part of cocktail treatment regimens for breast cancer patients. Topoisomerase inhibitors act as antineoplastic agents by binding to the DNA/enzyme complex inhibiting the action of topoisomerase, thus leaving behind a single strand of DNA. Multiple DNA-strand breaks lead to cell death but these breaks, which are repaired by chromosomal translocation, initiate leukemogenesis [1].
t-AL constitutes 10-20% of all cases of AL [1]. However, only sporadic cases of t-AL after systemic chemotherapy have been reported in Korea [6]. Although many epidemiologic studies have been conducted in other countries, no such literature exists on t-AL in the Korean population. Herein, we report the clinical characteristics, chromosomal findings, and bone marrow test results of 12 cases of t-AL that developed after topoisomerase inhibitor therapy in breast cancer patients in a single institute.
We reviewed the electronic medical records of patients who were primarily diagnosed with breast cancer and later developed AL and underwent treatment at the Asan Medical Center, Seoul, Korea, from 1989 to October 2009. A total of 9,228 patients were diagnosed and treated for breast cancer. Among them, 14 patients (0.2%) later developed t-AL. Two patients were excluded from this study: the therapeutic regimen of 1 patient did not include topoisomerase inhibitors and the other patient had been treated at a different hospital, and her medication history could not be evaluated. We retrospectively evaluated the medication record, history of radiation treatment, bone marrow test results, immunophenotypic results, and cytogenetic results of the included patients.
Peripheral blood and bone marrow aspirates were prepared with Wright-Giemsa staining for morphologic evaluation. Conventional panels were chosen for the analysis of AML and ALL markers and the FACSCanto flow cytometer (BectonDickinson, San Jose, CA, USA) was used.
Cytogenetic analysis was performed on bone marrow specimens using standard techniques. Giemsa-trypsin-Giemsa (GTG) banding was used to identify the chromosome. At least 20 metaphase cells were examined after 24-hr culture. The chromosomes were evaluated under 300-400 bands resolution according to the International System for Human Cytogenetic Nomenclature (2009) [7].
Event-free survival of 12 patients was analyzed. We divided the cases into the 11q23 rearranged group and non-11q23-involved group. The Wilcoxon test was used to plot the survival graph of the 2 groups.
Doxorubicin (Admycin; BoRyung Pharm, Seoul, Korea), which inhibits the progression of topoisomerase, was used in 12 patients. Alkylating agents were used together with doxorubicin in 10 patients. The participants were all female patients with a median age of 55 years. The period between completion of chemotherapy for breast cancer and diagnosis of t-AL was 18-95 months with a median period of 25 months. The patients' event-free survival after diagnosis of AL was 1-39 months. Five patients died, 3 patients are still alive, and 4 patients were lost to follow-up (Table 1).
Nine patients were diagnosed with therapy-related AML (t-AML) (75%, 9/12) and 3 patients (25%, 3/12) with therapy-related ALL (t-ALL). At the time of diagnosis, the average white blood cell count was 13,066/µL; median platelet count, 33,000/µL; median hemoglobin level, 7.6 g/dL; median percentage of blasts in the blood, 21%; and median percentage of blasts in the bone marrow aspirates, 79.2%. Leukemic blasts showed a "packed marrow" pattern with cellularity ranging from 75 to 100%.
One patient with mixed-lineage AML (case No. 7) showed 2 distinct populations of blasts (Fig. 1A) in the marrow aspirates. Also, her bone marrow biopsy revealed extensive myelofibrosis involving many myeloblasts and lymphoblasts (Fig. 1B). In another patient (case No. 3) diagnosed with t-MN, the percentage of blasts in the bone marrow aspirate was only 11.2%, and her bone marrow biopsy showed "packed marrow" infiltration of myeloid cells with variable maturation stages and scattered myeloblasts (Fig. 2).
Eight patients (67%, 8/12) had translocation of 11q23 (
We analyzed the event-free survival of 12 patients. We divided the cases into 2 groups, the 11q23-rearranged group and the non-11q23-involved group. The Wilcoxon test was used to plot the survival graph of the 2 groups; the graph showed that the 11q23 group had significantly poorer survival (
In this study, we selected cases with a history of treatment with a topoisomerase inhibitor prior to the onset of acute leukemia. Among the 12 patients treated with a topoisomerase inhibitor, 8 patients (67%) displayed a balanced translocation of the
The survival analysis of our cases showed that t-AL with 11q23 rearrangement presented poor prognosis. t-AL cases with 11q23 rearrangements are known for poor prognosis and 1 study showed that only 80% of patients achieved remission and 75% of them relapsed within 1 year [9]. Chen et al. reviewed t-ALL cases reported in the literature and concluded that the prognosis of t-ALL was much poorer compared to t-AML [10]. They also noted that survival did not differ between the 11q23 group and non-11q23 group in t-ALL patients. The overall prognosis in t-ALL was poor, regardless of the presence or absence of 11q23 abnormalities. Although our cases are limited in number, 1 patient with 11q23-involved t-ALL (case No. 10) had a relatively long event-free survival (27 months) compared to the other 2 t-ALL patients.
The MLL protein transcribed by the
Our study revealed that the incidence of t-AL among patients treated for breast cancer was 0.2%. A German study reported a rate of 0.2-0.5% of t-AL among breast cancer patients [16]. Such incidence rate suggests that there might be specific predisposing factors for t-AL. Host-associated factors have been hypothesized, including heritable predisposition due to enzymatic polymorphisms in genes involved in DNA repair or drug metabolism [17, 18]. Polymorphisms in the gene of phase I enzymes, mainly the CYP family and phase II enzymes, are associated with decreased enzymatic activity in t-AL. Reduced activity of these enzymes and reduced detoxification result in increased production of activated metabolites and increased toxicity of chemotherapy [19]. Another mechanism of secondary leukemogenesis is DNA repair defects. Its susceptibility may be based on polymorphisms of DNA repair and synthesis, leading to incomplete repair and persistence of mutations [18].
Other than hereditary predispositions, Martin et al. suggested that younger age and advanced stage of breast cancer predispose t-AML because these patients require higher doses of chemotherapeutic agents leading to t-AML [20]. In addition, they speculated on the possibility that early-onset breast cancer may have a genetic predisposition to t-AL and questioned the role mutations in the BRCA1 and 2 genes might play in the development of t-AL. The hypothesis could not be applied in our study because the participants were middle-aged women. Praga et al. reviewed 9,796 breast cancer patients and reported that the cumulative probability of developing AML/myelodysplastic syndrome (MDS) was 0.37% in patients treated with standard regimens, whereas the probability increased to 4.97% in those treated with higher doses of topoisomerase inhibitors. The dosage of chemotherapeutic agents had a significant effect on the development of t-AL [21].
Several studies showed that combined radiotherapy and chemotherapy increased the risk of t-AL [22], whereas some suggested that limited-field radiation in the therapeutic dose range has very little or no effect on the risk of t-AL [1]. In our study, 8 patients had received radiation therapy and we did not observe a statistically significant effect on survival or latency period between completion of chemotherapy and diagnosis of t-AL.
t-AML represents 10-20% of all AML cases [23], whereas t-ALL accounts for 2.3% of all ALL cases [24]. t-ALL accounts for a much lower proportion of cases of secondary leukemia than t-AML. The incidence of t-AML (75%) was higher than that of t-ALL (25%) in our study. The WHO distinguishes t-MNs as a distinct category, although ALL may also arise secondary to cancer therapy. Some groups reported that t(4;11) is associated with t-ALL, whereas t(9;11) is generally found in t-AML [25]. One case (case No. 10) with t-ALL with 11q23 abnormality showed t(4;11) which is in agreement with the report. A review of the literature revealed that 11q23 aberration was not observed in nearly one third of reported cases of t-ALL treated with topoisomerase inhibitors [10]. This finding indicates that mechanisms other than 11q23 aberration may also contribute to the t-ALL induced by topoisomerase inhibitors.
In our study, 10 patients were treated with both a topoisomerase inhibitor and an alkylating agent. However, most cases presented with either 11q23 aberration or a short latency period between completion of chemotherapy and diagnosis of t-AL, i.e., patients with t-AL induced by a topoisomerase inhibitor. t-AL induced by alkylating agents generally presents with a longer latency period (5-7 years), preceding myelodysplastic features and frequent deletion of chromosomes 5, 5q, and/or 7, 7q [3]. The reason for the larger effect of topoisomerase inhibitors compared to alkylating agents remains unclear. Other factors such as dosage of each neoplastic agent might have had an effect.
Our presentation of 12 cases showed various features of t-AL after treatment with a topoisomerase inhibitor. We also observed that various types of AML were diagnosed other than myelomonocytic leukemia which is known to be the most prevalent type in AML associated with
Mixed lineage AML (Case No. 7).
Therapy-related myeloid neoplasm (Case No. 3).
Event-free survival plot of 11q23 group vs. non-11q23 group, showing significantly poorer survival of the 11q23 translocated group (
Table 1 Demographics and laboratory findings of 12 patients.
Abbreviations: A, Admycin (doxorubicin hydrochloride); C, Alkyloxan (cyclophosphamide); F, 5FU (fluorouracil); CIS, Cisplatin; TAC, Taxol (paclitaxel); VCS, vincristine sulfate; RTx, radiation treatment; AML, acute myeloid leukemia; ALL, acute lymphoblastic leukemia; TdT, terminal deoxynucleotidyl transferase; HLA, human leukocyte antigen.
Korean J Hematol 2010; 45(3): 177-182
Published online September 30, 2010 https://doi.org/10.5045/kjh.2010.45.3.177
Copyright © The Korean Society of Hematology.
Hyoeun Shim1, Hyun-Sook Chi1*, Seongsoo Jang1, Eul-Ju Seo1, Chan-Jeoung Park1, Jung-Hee Lee2, Je-Hwan Lee2, and Kyoo-Hyung Lee2
1Department of Laboratory Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
2Department of Internal Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
Correspondence to: Correspondence to Hyun-Sook Chi, M.D., Ph.D. Department of Laboratory Medicine, Asan Medical Center, 86 Asanbyeongwon-gil, Songpa-gu, Seoul 138-736, Korea. Tel: +82-2-3010-4502, Fax: +82-2-478-0884, hschi@amc.seoul.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Therapy-related myeloid neoplasm (t-MN) is a distinct class of acute myeloid leukemia (AML) in the World Health Organization (WHO) classification. Both AML and acute lymphoblastic leukemia (ALL) may develop after treatment for primary cancer. Topoisomerase inhibitors are commonly used to treat breast cancer patients and are well-known for their effect on leukemogenesis of therapy-related acute leukemias (t-AL).
We retrospectively evaluated bone marrow test results, chromosomal findings, and clinical characteristics of 12 patients who received topoisomerase inhibitors for breast cancer treatment and later developed acute leukemia.
Fourteen patients (0.2%) developed t-AL after treatment for breast cancer. Topoisomerase inhibitors were administered to 12 patients. Among them, 9 patients (75%, 9/12) were diagnosed with therapy-related AML (t-AML) and 3 patients (25%, 3/12) with therapy-related ALL (t-ALL). Eight patients (67%, 8/12) showed translocation involving 11q23 and 3 different partner genes, 19p13.1 (37.5%, 3/8), 9p22 (37.5%, 3/8), and 4q21 (25%, 2/8). The median interval between completion of chemotherapy for breast cancer and occurrence of t-AL was 25 months. Patients with 11q23 translocation showed markedly poorer event-free survival than the group without involvement of 11q23.
The incidence rate of t-AL after treatment for breast cancer was 0.2% in a tertiary hospital in Korea. Translocation involving the
Keywords: Therapy-related acute myeloid leukemia, Breast cancer, Topoisomerase inhibitors, 11q23
Therapy-related acute leukemia (t-AL) is the most severe complication that may occur after treatment for primary cancer. It is diagnosed on the basis of histories of treatment and molecular abnormalities, and develops after chemotherapy, radiation, or immunosuppressive agents performed for the management of the primary cancer [1]. The World Health Organization (WHO) recognizes therapy-related myeloid neoplasm (t-MN) as a distinct subtype of acute myeloid leukemia (AML), although acute lymphoblastic leukemia (ALL) may also arise [2]. Topoisomerase inhibitors and alkylating agents are 2 well-known antineoplastic agents that cause t-AL [3].
The incidence rate of t-AL among patients treated for breast cancer has been reported to be 0.2-0.5% [4]. Breast cancer is the second most common cancer in Korean women, and such serious side effects are a matter of concern [5]. Topoisomerase inhibitors are part of cocktail treatment regimens for breast cancer patients. Topoisomerase inhibitors act as antineoplastic agents by binding to the DNA/enzyme complex inhibiting the action of topoisomerase, thus leaving behind a single strand of DNA. Multiple DNA-strand breaks lead to cell death but these breaks, which are repaired by chromosomal translocation, initiate leukemogenesis [1].
t-AL constitutes 10-20% of all cases of AL [1]. However, only sporadic cases of t-AL after systemic chemotherapy have been reported in Korea [6]. Although many epidemiologic studies have been conducted in other countries, no such literature exists on t-AL in the Korean population. Herein, we report the clinical characteristics, chromosomal findings, and bone marrow test results of 12 cases of t-AL that developed after topoisomerase inhibitor therapy in breast cancer patients in a single institute.
We reviewed the electronic medical records of patients who were primarily diagnosed with breast cancer and later developed AL and underwent treatment at the Asan Medical Center, Seoul, Korea, from 1989 to October 2009. A total of 9,228 patients were diagnosed and treated for breast cancer. Among them, 14 patients (0.2%) later developed t-AL. Two patients were excluded from this study: the therapeutic regimen of 1 patient did not include topoisomerase inhibitors and the other patient had been treated at a different hospital, and her medication history could not be evaluated. We retrospectively evaluated the medication record, history of radiation treatment, bone marrow test results, immunophenotypic results, and cytogenetic results of the included patients.
Peripheral blood and bone marrow aspirates were prepared with Wright-Giemsa staining for morphologic evaluation. Conventional panels were chosen for the analysis of AML and ALL markers and the FACSCanto flow cytometer (BectonDickinson, San Jose, CA, USA) was used.
Cytogenetic analysis was performed on bone marrow specimens using standard techniques. Giemsa-trypsin-Giemsa (GTG) banding was used to identify the chromosome. At least 20 metaphase cells were examined after 24-hr culture. The chromosomes were evaluated under 300-400 bands resolution according to the International System for Human Cytogenetic Nomenclature (2009) [7].
Event-free survival of 12 patients was analyzed. We divided the cases into the 11q23 rearranged group and non-11q23-involved group. The Wilcoxon test was used to plot the survival graph of the 2 groups.
Doxorubicin (Admycin; BoRyung Pharm, Seoul, Korea), which inhibits the progression of topoisomerase, was used in 12 patients. Alkylating agents were used together with doxorubicin in 10 patients. The participants were all female patients with a median age of 55 years. The period between completion of chemotherapy for breast cancer and diagnosis of t-AL was 18-95 months with a median period of 25 months. The patients' event-free survival after diagnosis of AL was 1-39 months. Five patients died, 3 patients are still alive, and 4 patients were lost to follow-up (Table 1).
Nine patients were diagnosed with therapy-related AML (t-AML) (75%, 9/12) and 3 patients (25%, 3/12) with therapy-related ALL (t-ALL). At the time of diagnosis, the average white blood cell count was 13,066/µL; median platelet count, 33,000/µL; median hemoglobin level, 7.6 g/dL; median percentage of blasts in the blood, 21%; and median percentage of blasts in the bone marrow aspirates, 79.2%. Leukemic blasts showed a "packed marrow" pattern with cellularity ranging from 75 to 100%.
One patient with mixed-lineage AML (case No. 7) showed 2 distinct populations of blasts (Fig. 1A) in the marrow aspirates. Also, her bone marrow biopsy revealed extensive myelofibrosis involving many myeloblasts and lymphoblasts (Fig. 1B). In another patient (case No. 3) diagnosed with t-MN, the percentage of blasts in the bone marrow aspirate was only 11.2%, and her bone marrow biopsy showed "packed marrow" infiltration of myeloid cells with variable maturation stages and scattered myeloblasts (Fig. 2).
Eight patients (67%, 8/12) had translocation of 11q23 (
We analyzed the event-free survival of 12 patients. We divided the cases into 2 groups, the 11q23-rearranged group and the non-11q23-involved group. The Wilcoxon test was used to plot the survival graph of the 2 groups; the graph showed that the 11q23 group had significantly poorer survival (
In this study, we selected cases with a history of treatment with a topoisomerase inhibitor prior to the onset of acute leukemia. Among the 12 patients treated with a topoisomerase inhibitor, 8 patients (67%) displayed a balanced translocation of the
The survival analysis of our cases showed that t-AL with 11q23 rearrangement presented poor prognosis. t-AL cases with 11q23 rearrangements are known for poor prognosis and 1 study showed that only 80% of patients achieved remission and 75% of them relapsed within 1 year [9]. Chen et al. reviewed t-ALL cases reported in the literature and concluded that the prognosis of t-ALL was much poorer compared to t-AML [10]. They also noted that survival did not differ between the 11q23 group and non-11q23 group in t-ALL patients. The overall prognosis in t-ALL was poor, regardless of the presence or absence of 11q23 abnormalities. Although our cases are limited in number, 1 patient with 11q23-involved t-ALL (case No. 10) had a relatively long event-free survival (27 months) compared to the other 2 t-ALL patients.
The MLL protein transcribed by the
Our study revealed that the incidence of t-AL among patients treated for breast cancer was 0.2%. A German study reported a rate of 0.2-0.5% of t-AL among breast cancer patients [16]. Such incidence rate suggests that there might be specific predisposing factors for t-AL. Host-associated factors have been hypothesized, including heritable predisposition due to enzymatic polymorphisms in genes involved in DNA repair or drug metabolism [17, 18]. Polymorphisms in the gene of phase I enzymes, mainly the CYP family and phase II enzymes, are associated with decreased enzymatic activity in t-AL. Reduced activity of these enzymes and reduced detoxification result in increased production of activated metabolites and increased toxicity of chemotherapy [19]. Another mechanism of secondary leukemogenesis is DNA repair defects. Its susceptibility may be based on polymorphisms of DNA repair and synthesis, leading to incomplete repair and persistence of mutations [18].
Other than hereditary predispositions, Martin et al. suggested that younger age and advanced stage of breast cancer predispose t-AML because these patients require higher doses of chemotherapeutic agents leading to t-AML [20]. In addition, they speculated on the possibility that early-onset breast cancer may have a genetic predisposition to t-AL and questioned the role mutations in the BRCA1 and 2 genes might play in the development of t-AL. The hypothesis could not be applied in our study because the participants were middle-aged women. Praga et al. reviewed 9,796 breast cancer patients and reported that the cumulative probability of developing AML/myelodysplastic syndrome (MDS) was 0.37% in patients treated with standard regimens, whereas the probability increased to 4.97% in those treated with higher doses of topoisomerase inhibitors. The dosage of chemotherapeutic agents had a significant effect on the development of t-AL [21].
Several studies showed that combined radiotherapy and chemotherapy increased the risk of t-AL [22], whereas some suggested that limited-field radiation in the therapeutic dose range has very little or no effect on the risk of t-AL [1]. In our study, 8 patients had received radiation therapy and we did not observe a statistically significant effect on survival or latency period between completion of chemotherapy and diagnosis of t-AL.
t-AML represents 10-20% of all AML cases [23], whereas t-ALL accounts for 2.3% of all ALL cases [24]. t-ALL accounts for a much lower proportion of cases of secondary leukemia than t-AML. The incidence of t-AML (75%) was higher than that of t-ALL (25%) in our study. The WHO distinguishes t-MNs as a distinct category, although ALL may also arise secondary to cancer therapy. Some groups reported that t(4;11) is associated with t-ALL, whereas t(9;11) is generally found in t-AML [25]. One case (case No. 10) with t-ALL with 11q23 abnormality showed t(4;11) which is in agreement with the report. A review of the literature revealed that 11q23 aberration was not observed in nearly one third of reported cases of t-ALL treated with topoisomerase inhibitors [10]. This finding indicates that mechanisms other than 11q23 aberration may also contribute to the t-ALL induced by topoisomerase inhibitors.
In our study, 10 patients were treated with both a topoisomerase inhibitor and an alkylating agent. However, most cases presented with either 11q23 aberration or a short latency period between completion of chemotherapy and diagnosis of t-AL, i.e., patients with t-AL induced by a topoisomerase inhibitor. t-AL induced by alkylating agents generally presents with a longer latency period (5-7 years), preceding myelodysplastic features and frequent deletion of chromosomes 5, 5q, and/or 7, 7q [3]. The reason for the larger effect of topoisomerase inhibitors compared to alkylating agents remains unclear. Other factors such as dosage of each neoplastic agent might have had an effect.
Our presentation of 12 cases showed various features of t-AL after treatment with a topoisomerase inhibitor. We also observed that various types of AML were diagnosed other than myelomonocytic leukemia which is known to be the most prevalent type in AML associated with
Mixed lineage AML (Case No. 7).
Therapy-related myeloid neoplasm (Case No. 3).
Event-free survival plot of 11q23 group vs. non-11q23 group, showing significantly poorer survival of the 11q23 translocated group (
Table 1 . Demographics and laboratory findings of 12 patients..
Abbreviations: A, Admycin (doxorubicin hydrochloride); C, Alkyloxan (cyclophosphamide); F, 5FU (fluorouracil); CIS, Cisplatin; TAC, Taxol (paclitaxel); VCS, vincristine sulfate; RTx, radiation treatment; AML, acute myeloid leukemia; ALL, acute lymphoblastic leukemia; TdT, terminal deoxynucleotidyl transferase; HLA, human leukocyte antigen..
Young Lan Kwon, Jae Kwon Joeng, Ga Young Kim, Sae Rom Kim, Se Young Lee, Young Deuk Youn, Jung Lim Lee, Won Sik Lee, Gun Young Kwon, Jae Hoo Park
Korean J Hematol 2006; 41(2): 134-136
Mixed lineage AML (Case No. 7).
Therapy-related myeloid neoplasm (Case No. 3).
Event-free survival plot of 11q23 group vs. non-11q23 group, showing significantly poorer survival of the 11q23 translocated group (