Monitoring of minimal residual disease (MRD) is useful to predict prognosis of adult patients with Ph-negative ALL: results of a prospective study (ALL MRD2002 Study)
- Koji Nagafuji1Email author,
- Toshihiro Miyamoto2,
- Tetsuya Eto3,
- Tomohiko Kamimura4,
- Shuichi Taniguchi5,
- Takashi Okamura1,
- Eiichi Ohtsuka6,
- Takashi Yoshida7,
- Masakazu Higuchi8,
- Goichi Yoshimoto9,
- Tomoaki Fujisaki10,
- Yasunobu Abe11,
- Yasushi Takamatsu12,
- Shouhei Yokota13,
- Koichi Akashi2 and
- Mine Harada14
© Nagafuji et al.; licensee BioMed Central Ltd. 2013
Received: 27 December 2012
Accepted: 3 February 2013
Published: 6 February 2013
Allogeneic hematopoietic stem cell transplantation (HSCT) for patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL) in first complete remission (CR1) is much more intensive than multi-agent combined chemotherapy, although allogeneic HSCT is associated with increased morbidity and mortality when compared with such chemotherapy. Minimal residual disease (MRD) status has been proven to be a strong prognostic factor for adult patients with Ph-negative ALL.
We investigated whether MRD status in adult patients with ALL is useful to decide clinical indications for allogeneic HSCT. We prospectively monitored MRD after induction and consolidation therapy in adult patients with Ph-negative ALL.
Of 110 adult ALL patients enrolled between July 2002 and August 2008, 101 were eligible, including 59 Ph-negative patients. MRD status was assessed in 43 patients by the detection of major rearrangements in TCR and Ig and the presence of chimeric mRNA. Thirty-nine patients achieved CR1, and their probabilities of 3-year overall survival and disease-free survival (DFS) were 74% and 56%, respectively. Patients who were MRD-negative after induction therapy (n = 26) had a significantly better 3-year DFS compared with those who were MRD-positive (n = 13; 69% vs. 31%, p = 0.004). All of 3 patients who were MRD-positive following consolidation chemotherapy and did not undergo allogeneic HSCT, relapsed and died within 3 years after CR.
These results indicate that MRD monitoring is useful for determining the clinical indications for allogeneic HSCT in the treatment of ALL in CR1.
Although more than 80% of adult patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL) achieve complete remission (CR) with conventional induction therapy, their 5-year survival is only 30%–40%. Leukemia relapse is the most common cause of treatment failure in ALL [1–6]. Therefore, post-remission therapy is necessary and should be optimized in the treatment of adult ALL patients. If prognosis of patients with ALL in CR1 is estimated to be favorable, chemotherapy is usually continued to prevent leukemia relapse. However, patients with less favorable prognosis should be treated more aggressively . Although allogeneic hematopoietic stem cell transplantation (HSCT) for patients with ALL in CR1 is much more intensive than multi-agent combined chemotherapy, it is associated with increased morbidity and mortality when compared with such chemotherapy.
Minimal residual disease (MRD) status has been proven to be a strong prognostic factor for adult patients with Ph-negative ALL [8–14]. In this study, we prospectively monitored the MRD status after CR induction and consolidation chemotherapies in adult patients with Ph-negative ALL to determine the clinical indications for allogeneic HSCT.
Patients & methods
Patient eligibility criteria
A total of 110 adult ALL patients were enrolled in this study between July 2002 and August 2008 on the basis of the following eligibility criteria: non-L3 ALL, 16–65 years of age, an Eastern Cooperative Oncology Group performance status of 0–2, and adequate liver and kidney function (serum bilirubin, ≤2.0 mg/dl and serum creatinine, ≤2.0 mg/dl, respectively). Cytogenetic studies were performed on pretreated bone marrow or unstimulated blood samples using the standard banding technique. The treatment protocol was approved by the institutional review board of each participating hospital. Written informed consent was obtained from all patients in accordance with the Declaration of Helsinki. Of the 110 patients enrolled, 42 were excluded from the study because of Ph-positivity, 5 because of misdiagnosis, 2 because of infectious complications, and 1 each because of liver damage and protocol violation. The remaining 59 patients were Ph- negative.
We used a modified CALGB 19802 [15, 16] treatment protocol that comprised 6 courses of chemotherapy administered in the order of A-B-C-A-B-C regimens, followed by a maintenance phase. Induction chemotherapy (course A) was a 21-day course consisting of cyclophosphamide (CPM; 1200 mg/m2 on day 1), daunorubicin (DNR; 60 mg/m2 on days 1, 2, and 3), vincristine (VCR;1.3 mg/m2 [maximum 2 mg] on days 1, 8, 15, and 22), L-asparaginase (3000 U/m2 on days 9, 11, 13, 16, 18, and 20), and prednisolone (PSL; 60 mg/m2 [max 100 mg]). Granulocyte-colony stimulating factor (nartograstim) was administered starting from day 4 and continued until neutrophil recovery. For patients aged 55 years or older, the doses of CPM and DNR were reduced to 500 mg/m2 and 50 mg/m2, respectively. Furthermore, PSL therapy was shortened to 7 days in these patients. The first consolidation therapy (course B) consisted of mitoxantrone (MIT; 10 mg/m2 on days 2 and 3), cytarabine (AraC; 2000 mg/m2/day on days 1, 2, 3, and 4) and intrathecal administration of methotrexate (MTX; 15 mg/body on day 1). For patients aged 55 years or older, the doses of MIT and AraC were reduced to 7 mg/m2 and 1500 mg/m2/day, respectively. The second consolidation therapy (course C) consisted of VCR (1.3 mg/m2 [max 2 mg] on days 1, 8, and 15) and MTX (1500 mg/m2 on days 1, 8, and 15) with leucovorin rescue and intrathecal MTX on days 1, 8, and 15. The patients received the following maintenance chemotherapy on a monthly basis: PSL, 60 mg/m2 on days 1–5; VCR, 1.3 mg/m2 (max 2 mg) on day 1; oral MTX, 20 mg/m2 weekly; and oral 6-mercaptopurine, 60 mg/m2 daily. MRD status was evaluated after the induction therapy (first course A) and after the second consolidation therapy (first course C). Patients with positive MRD following the second consolidation therapy were considered to be indicated for allogeneic HSCT as soon as possible. Eligible donors included HLA-identical related, HLA-identical unrelated donors from Japan Marrow Donation Program, and cord blood from Japan Cord Blood Bank Network. Conditioning before allogeneic HSCT and prophylaxis for graft-versus-host disease was performed according to each institutional standard.
Real-time quantitative polymerase chain reaction (RQ-PCR) analysis of chimeric mRNA
mRNA from bone marrow cells were analyzed for the presence of major and minor BCR/ABL, TEL/AML1, MLL/AF4, MLL/AF9, MLL/AF6, MLL/ENL, E2A/PBX1, and SIL/TAL1 chimeric genes. Samples were amplified by RQ-PCR and quantified by parallel amplification of serial dilutions of transcript-containing plasmids [17, 18].
PCR analysis of TCR/Ig rearrangement
High-molecular weight DNA from marrow cells was initially screened for major rearrangement patterns of TCRγ, TCRδ, and Igκ, and secondarily screened for rearrangements in Ig heavy chain (IgH), using previously described primers [19–21]. Two-step (nested) PCR for MRD quantification was performed using allele-specific oligonucleotide (ASO)-primers based on the sequence of PCR screening products, which had clonal recombinations by heteroduplex analyses. Prior to PCR analysis, DNA samples from post-treatment bone marrow samples and DNA from the samples obtained at diagnosis were serially diluted (between 10−2 and 10−5) with buffy coat DNA from eight healthy volunteers. Buffy coat DNA was also used as a control for nonspecific amplification of comparable Ig/TCR arrangements present in normal cells. All PCR reactions were performed simultaneously and analyzed using ethidium staining and agarose gel electrophoresis. MRD was quantified by comparing the intensities of band signals on an agarose gel stained with ethidium bromide without amplification of the background. MRD quantifications were performed using ASO-primers with a sensitivity of ≤1 × 10−4, and MRD positivity was defined as a lower limit of detection of ≥1 × 10−3.
Statistical analyses of the data accumulated throughout October 2011 were performed. Overall survival (OS) was defined as the time between diagnosis and the end of the trial or death, and disease-free survival (DFS) was defined as the time from CR to relapse or death while still in CR. Survival curves were estimated using the Kaplan–Meier method, and the statistical significance of differences in survival was determined using the log-rank test.
The influence of prognostic factors including age, white blood cell (WBC) count, and MRD status on DFS was estimated with multivariate Cox regression analysis. The level of statistical significance was set at 0.05.
Patient characteristics and clinical outcome
Ph negative & known MRD status
Total No. patients
Sex, No. (%)
Median Age, (range)
Median WBC count, ×109/L, (range)
Immunophenotype, No. (%)
CR rate, No. (%)
3-years OS (%)
3-years DFS (%)
Relationship between MRD status and treatment outcomes
Multivariate analysis for disease-free survival (Cox Regression Model)
MRD status after induction
MRD status after consolidation
Compared with treatments for childhood ALL, those for adult ALL are far less effective , and allogeneic HSCT is frequently recommended as the most potent post-remission therapy for ALL patients in CR1 . Since relapse in ALL patients leads to very poor prognosis [24–26], the notion that allogeneic HSCT should be performed for all patients with ALL beyond CR1 is difficult to be realized in clinical situations .
The international ALL trial MRC UKALL XII/ECOG E2993 showed that allogeneic HSCT using matched related donors provided survival benefit for standard-risk adult patients with Ph-negative ALL in CR1 compared with chemotherapy, while there was no significant survival benefit for high-risk patients. Allogeneic HSCT is able to reduce relapse rates in both standard-risk and high-risk patients; however, there is a decrease in OS in the high-risk patients because of their higher rates of transplant-related mortality. The high-risk in this international study was defined as having as 1 of the following factors: age more than 35 years, a high WBC count at presentation (>30 × 109/L for B lineage and >100 × 109/L for T lineage) . Age is a significant prognostic factor for ALL patients receiving allogeneic HSCT as well as chemotherapy . Therefore, allogeneic HSCT may not be a recommended option for patients defined as high-risk because of their age being more than 35 years old [28, 29].
Recent studies have shown that a pediatric-inspired ALL chemotherapy protocol significantly improves treatment outcome in relatively young adult ALL patients [30–34], and this patient population is at standard-risk in terms of age. Thus, the indication of allogeneic HSCT based on the risk stratification made by initial presentation needs to be tested, and more reliable indication for allogeneic HSCT in adult patients with Ph-negative ALL in CR1 is necessary.
MRD measurement in adult patients with Ph-negative ALL has been reported to be useful for identifying patients with a significantly high risk of relapse. The German Multicenter Study Group for adult ALL (GMALL) study used PCR analysis of antigen-receptor genes to assess MRD in standard-risk ALL patients. Low-risk patients were those with MRD–negative on days 11 and 24 and had a 3-year relapse rate of 0%; high-risk patients were those with MRD-positive until week 16 and had a relapse rate of 94% . The Northern Italy Leukemia Group-ALL 09/00 study found that MRD was the most significant predictor of relapse . The estimated 5-year DFS was 72% in 58 MRD-negative patients at the end of consolidation and 14% in 54 MRD-positive patients.
Our results indicate that patients with MRD negativity after induction therapy provided excellent DFS without allogeneic HSCT, whereas patients with MRD positivity after several consolidation therapies showed very poor DFS if they did not undergo allogeneic HSCT. This observation is in line with above reports. Our analysis showed that late-attained MRD negativity could not lead to good prognosis, while other groups reported the MRD negativity at the end of consolidation to be associated with good prognosis. This controversy may reflect the sensitivity level of MRD measurement. We used semi-quantitative PCR analysis and defined MRD negativity as <1 × 10−3, whereas GMALL  and The Northern Italy Leukemia Group-ALL 09/00 study  analyzed MRD according to EuroMRD-ALL guidelines [35, 36] and considered <1 × 10−4 as MRD negativity. In our study, MRD positivity after the second course of consolidation was seen in 6 of 37, while MRD positivity at the end of consolidation was observed in 54 of 112 in The Northern Italy Leukemia Group-ALL study 09/00 . Thus, our MRD-negative patients had a possibility of MRD positivity if more sensitive MRD analysis was used. We suggest these late-attained MRD-negative patients were potential candidates for allogeneic HSCT.
In this study, the results of multivariate Cox regression analysis for DFS indicates that age (≥35 years vs. <35 years) and MRD status after induction therapy were significant prognostic factors, whereas WBC count (≥30 × 109/L vs. <30 × 109/L) or MRD status after consolidation therapy was not. Age is one of the most important prognostic factors in adult ALL patients, and age of our study population was median 31 years-old ranging 17 to 63 including adolescent and young adult patients. Thus, these relative young patients were supposed to have good prognosis with chemotherapy. Initial WBC count has been another important prognostic factor in adult ALL patients, but not in our study. Our chemotherapy regimen was modified CALGB 19802 with dose intensification of daunorubicin and cytarabine, and it might be possible that this intensive chemotherapy conquer negative impact of high initial WBC count. According to the recently reported result of CALGB 19802 , age (≥60 years vs. <60 years) was a significant prognostic factor for DFS, while initial WBC count (≥30 × 109/L vs. <30 × 109/L) was not. This report was in line with our observation. In our analysis MRD status after induction therapy (positive vs. negative: HR 8.769, and p < 0.001) was a very strong prognostic factor for DFS. Whether negative impact of MRD positivity could be overcome by allogeneic HSCT is the next consideration. There are two reports regarding the effect of prospective allocation for allogeneic HSCT based on MRD positivity in adult patients with Ph-negative ALL in CR1.
In the Northern Italy Leukemia Group-ALL study 09/00, for the MRD-positive patients at the end of consolidation, there was a significantly better 4-year DFS for 36 patients who had an allogeneic (n = 22) and autologous (n = 14) HSCT compared to 18 patients unable to undergo HSCT (33% vs. 0%, p = 0.0000) . The GMALL reported that 5-year DFS for MRD-positive patients at week 16 with (n = 57) vs. without (n = 63) allogeneic HSCT were 44 ± 8% vs. 11 ± 4% respectively (p <0.0001) . In our study, among MRD-positive patients following consolidation chemotherapy C in the first course, all of 3 patients without allogeneic HSCT relapsed while 1 of 3 patients with allogeneic HSCT did. The size of our study population was too small for statistical analysis. However, these three studies clearly indicate that MRD-positive patients at late phase of chemotherapy have little chance of DFS more than 10% without allogeneic HSCT . These MRD-defined high-risk patients had much worse prognosis compared with conventional high-risk patients defined by initial presentation. Furthermore, allocation of allogeneic HSCT could improve the prognosis of MRD-defined high-risk patients.
The interpretation of our results may be affected by a limited number of adult ALL patients. A role of MRD measurement should be evaluated in relation with patients’ geography, chemotherapy regimens used, and timing and sensitivity of MRD analysis. With our less sensitive MRD analysis compared to EuroMRD-ALL guidelines, we could identify patients with good early treatment response not indicated for allogeneic HSCT, while we could not identify patients with good late treatment response. In near future, the assessment of MRD status using standardized protocols and RQ-PCR [35, 36] will be a valuable tool to stratify a risk of relapse in adult patients with Ph-negative ALL in CR1.
In conclusion, our data suggest that evaluation of MRD at least twice after induction and consolidation is very useful when considering clinical indication for allogeneic HSCT in adult patients with Ph-negative ALL in CR1.
This clinical study was a collaborative investigation with Kyushu University and Kyowa Hakko Kirin Co., Ltd.
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