Minimal Residual Disease in Acute Myeloid Leukemia (AML) and Hematopoietic Stem Cell Transplantation (HSCT) - A Retrospective Study

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 4469-4469
Author(s):  
Maura Valerio Ikoma ◽  
Vergílio Antônio Rensi Colturato ◽  
Camila Marques ◽  
Marcimara Penitenti ◽  
Anderson João Simione ◽  
...  

Abstract Abstract 4469 Minimal Residual Disease (MRD) is an important criterion to define risk of relapse in Acute Leukemia (AL). The most powerful methods for MRD characterization are PCR, and flow cytometry (FCM). Although PCR is more sensible that FCM, respectively 10−4 and 10−3 logs, FCM is more applicable than PCR, usually more than 80% versus less than 50% to PCR. In patients eligible for HSTC, the value of MRD is being studied and some results showed implications both in overall survival (OS) as in event free survival (EFS). The RCI seems to be influenced by the presence or absence of MRD, as well. Nowadays the most important factor that influences survival is the relapse. Then, the earlier relapse detection has a potential to improve the therapeutic results. We presented the results of MRD before and after HSTC and its prognostic significance. Other evaluated factors were: age, acute and chronic GVHD (aGVHD and cGVHD), cell source (bone marrow, peripheral blood, cord blood), ATG use, myeloablative conditioning or not, related (RD) and unrelated donor (UD), donor gender and disease status. Bone marrow of 112 AML patients were analyzed by FCM, since January/ 2008 until April / 2011. The evaluation was made in irregular period of time with variable number of samples by patients. They were from 1 to 61 years old. It was considered for analysis the patients that had MRD > 0,1% and < 5%. It was considered as negative result MRD < 0,1%. A dual laser FACSCalibur™ flow cytometer was used to data acquisition and analysis. Four color panels of monoclonal antibodies were chosen according the initial disease phenotype. Cell Quest Software was used for acquisition data and PAINT-A-GATE PRO and Infinicyt ™ for FMC analysis. It was done a live gate in reference markers and it was acquired a minimum of 500000 total events in each tube. Statistical analysis were performed by Kaplan Meier curves for OS e EFS and Cox regression. It was observed statistical significance in univariate analysis related to OS the following factors: RD (64%) × UR (42%) (p = 0,002), no ATG use (64%) × ATG use (44%) × (p = 0,003%), no aGVHD (63%) (p = 0,016) × aGVHD II to IV (50%), age > 40 years old (yo) (70%), 20 to 40 yo (59%) and < 20 yo (46%) (p = 0,048), MRD after HSCT <0,1% (77%) and > 0,1% (36%) (p=0,001) (fig 1). The other factors did not show statistical significance with a negative tendency to cord blood use (p = 0,079). To RCI, the significance was observed in: patient age < 21 yo (52%), 21 to 40 yo (30%) and > 40 yo (21%) (p=0,015); and MRD after TCTH > 0,1% (73%) × MRD < 0,1% (15%) (p = 0,000). Exerted statistical tendency: MRD < 0,1% before HSCT (p = 0,06), 1st remission (p = 0,07) and cGVHD (p = 0,08). The group of 44 patients that did not has MRD neither before or after HSCT showed OS of 85% in three years and 11% of RCI. The five morphologic relapses observed in this group suggest that a regular monitorization of MRD must be done. The only factor that kept statistical significance in multivariate analysis was MRD > 0,1% after TCTH in RCI (p = 0,001 HR = 9,93) and for OS (p = 0,001 HR = 3,77) (Tables 1 and 2). In conclusion, the presence of MDR > 0,1% was the only independent prognostic factor for survival and relapse in AML patients after HSCT. Disclosures: No relevant conflicts of interest to declare. Table 1:OS multivariate analysis Table 2:RCI multivariate analysis Figure 1: OS of patients after HSCT P = 0,000

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 4927-4927
Author(s):  
Herbert Henrique de Melo Santos ◽  
Glaciano Ribeiro ◽  
Allan de souza Santos ◽  
Marcos Chaves ◽  
Joanna Leal ◽  
...  

Abstract Introduction- Next generation flow (NGF) is one of the approaches for testing multiple myeloma (MM) minimal residual disease (MRD) over conventional response assessments. Actually, bone marrow (BM) is the preference site of evaluation because of its sensitivity. Because of its invasively technic, other possible sites for MRD evaluation outside the BM have been studied. In the present study we analyzed the MRD between the BM and the hematopoietic stem cell collected product (HSC product), once the concentration of plasma cell in the HSC product could be higher than peripheric blood sample. Aims- To compare MRD quantification of plasma cell between BM and HSC product after induction from Newly Diagnosed MM(NDMM) Transplant Eligible (TE) patients (pts) exposed to daratumumab, cyclophosphamide, thalidomide and dexamethasone (Dara-CTD) protocol. Methods- The SC product and BM samples were collected after four 28 days cycles of induction therapy from pts treated with Dara-CTd protocol described before by (Crusoe E. et al. Blood 2020; 136 (supplement 1): 17-18). MRD was evaluated by next-generation flow (NGF) based in the EuroFlow® protocol. EuroFlow standards was used to identify clonality and aberrant PC immune phenotype, consisting by EuroFlow 8-color 2-tube method (MM MRD kit, Cytognos, Salamanca), with the acquisition of 5 million events each tube and then merged into a single analysis tube on approximately 10 million events. Plasma cells were identified by CD38 multiepitope and CD138. Other markers were used to detect abnormal phenotypes. For comparison of MRD results, Bland-Altman plot comparing BM-MRD and HSC product-MRD was performed. Results- The first pts was enrolled in November 2018. A total of 24 pts were included, the median age was 60 (range 37- 67 years), 23 (92%) were non-white, 5 (21%) had an R-ISS = 1, 12 (54%) had an R-ISS = 2 and 4 (16%), an R-ISS = 3. Six (25%) pts had high-risk chromosomal abnormalities [del17p, t(4;14) or t(14;16)]. To date, all pts have completed induction and 20 have received transplant. Regarding response rates, after the end of induction (cycle 4), 19 (90%) of the pts obtained &gt; PR and 8 (38%) obtained &gt;VGPR, including three MRD negativity by NGF. 19 pts were analyzed for MRD. Negative MRD in sensitivity &lt;10 -5, &gt;=10 -5 and &lt;10 -4, &gt;=10 -4 evaluated in bone marrow was 4/19(21%), 4/19(21%), 11/19(58%) respectively. Negative MRD in sensitivity &lt;10 -5, &gt;=10 -5 and &lt;10 -4, &gt;=10 -4 evaluated in the HSC product was 13/19(68%), 3/19(16%), 3/19(16%) respectively. Median bone marrow sensitivity 10 -4 lower quartile 10 -5 upper quartile 10 -3. Normal distribution of the differences between BM and SC product MRD was first assessed (Kolmogorov-Smirnov's p &lt; 0.001, n = 19). Discussion-Conclusions- The use of HSC product could enhance the plasma cell concentration and may be an alternative and attractive method for MRD detection that diminished the invasiveness of repetitive bone marrow aspirations and tackling the heterogeneity distribution of MM cells. In this preliminary data the sample size did not allow to show a direct correlation between BM and HCS product. A larger sample would be needed to confirm the hypothesis. Figure 1 Figure 1. Disclosures Hungria: Amgen, BMS, Celgene, Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Support for attending meetings/travel ; Abbvie: Honoraria; Sanofi: Honoraria, Other: Support for attending meetings/travel ; Takeda: Honoraria. De Queiroz Crusoe: Janssen: Research Funding.


Blood ◽  
2020 ◽  
Author(s):  
Florian Chevillon ◽  
Emmanuelle Clappier ◽  
Chloe Arfeuille ◽  
Jean-Michel Cayuela ◽  
Jean-Hugues Dalle ◽  
...  

Ovarian tissue cryopreservation (OTC) is offered to women treated for acute leukemia to preserve their fertility before hematopoietic stem cell transplantation. The risk of leukemic infiltration in ovarian samples harvested before administration of chemotherapy limits ovarian tissue transplantations. We assessed the minimal residual disease (MRD) by sensitive quantitative polymerase chain reaction in cryopreserved ovarian cortex and medulla samples harvested from 30 patients in complete remission of acute leukemia, including 60 % with negative bone marrow MRD at the time of OTC. Ovarian MRD was undetectable in 21 patients (70%), detectable below 10-4 in 8 patients (27%) and between 10-3 and 10-4 in 1 patient (3%). Twenty patients (67%) had concordant MRD between bone marrow and ovarian samples. Interestingly 4 patients had positive MRD in ovarian samples while undetectable in bone marrow. Our results underline the importance of reaching the best control of the disease with undetectable or low MRD levels before OTC to minimize the risk of ovarian leukemic infiltration. The discordant results between ovarian samples and bone marrow require to test the more ovarian samples available before considering ovarian tissue transplantation.


Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 5786-5786
Author(s):  
Xingyu Cao ◽  
Deyan Liu ◽  
Jianping Zhang ◽  
Zhijie Wei ◽  
Min Xiong ◽  
...  

Abstract The level of minimal residual disease (MRD) is one of the most important prognostic indicators for acute lymphoblastic leukemia (ALL). In this study, the data about 390 cases of ALL patients who obtained MRD negative after chemotherapy or CART therapy underwent allogenic hematopoietic stem cell transplantation (HSCT) in our center were retrospectively analyzed. The MRD was detected by flow cytometry or molecular methods such as fusion genes or gene mutations. 235 were males and 155 were females. Median age was 15 years old (range 2-64). According to 2016 WHO classification, the diagnosis were Pro-B-ALL(n=24), Common B-ALL(n=113), Pre-B-ALL(n=17), Hyperdiploid (n=8), BCR-ABL positive B-ALL(n=51), MLL rearranged B-ALL (n=19), TEL-AML positive B-ALL (n=13), E2A-PBX B-ALL (n=16), BCR-ABL1-like B-All (n=4), Pro-T-ALL(n=8), Pre-T-AL(n=21), Cortical T-ALL(n=17), Medullary T-ALL (n=6) and ETP T-ALL(n=1). Other 5 patients have complex karyotypes and 67 patients cannot be grouped because of absence complete information about immunophenotypes or genetic profiles. Total number of B-ALL was 295 (54 of which received CART therapy before transplant.) and T-ALL was 92. Another one was T-B mixed lineage and remaining two's lineages was unknown. 14% of the patients had sibling identical donors (n=54), 66% of the patients had haplo-identical relative donors (n=258) and others are unrelated donor (n=77) or cord blood (n=1) transplantation. Disease status before transplant are CR1 (n=228), CR2(n=134) and ≥CR3(n=28). MNC dose was 8.30(2.50-22.60)×108/kg, CD34+cells dose was 4.51(0.89-19.61) ×106/kg and CD3+cells was 1.58(0.01-37.63) ×108/kg. Preparative regimens were based on TBI (n=352) or Bu (n=38). The median time to neutrophil and platelets engraftment was 14 and 12 days. Five-years OS and disease-free survival (DFS) for all patients were 71.7% and 71.1% . Univariate analysis showed difference of impact on overall survival about the patient' gender, age, T or B immunotype, WHO classification, whether or not receiving CART therapy before transplant, conditioning regimen based on TBI or Bu, years of transplant, and time from diagnosis to transplant (≤1year, >1year, ≤2year, >2year, ≤3year, >3year) was not statistically significant. 5-ys OS for CR1, CR2, >CR2 were 77.4%, 60.9%, 67.8% (p=0.0018). Five-years OS for sibling-identical , unrelated donor and haplo-identical transplant were 74.8%, 68.8% and 79.6% (p=0.026). The incidence of gradeⅠ-Ⅱ aGVHD and grade Ⅲ-ⅣaGVHD within 100 days were 1.5% and 2.1%. Limited cGVHD was 10.3% and extensive cGVHD was 9.2%. 5 years cumulative relapse rate was 12.2%. In summary, when MRD were negative before transplantation, the result of allo-HSCT for ALL is good. The factors affecting the survival rate are disease status and interval between diagnosis and transplant time rather than gender, age, WHO classification, immunotype, whether or not receiving CART therapy and conditioning regimen. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 2271-2271
Author(s):  
Eva Fronkova ◽  
Smadar Avigad ◽  
Ki Wai Chik ◽  
Luis Castillo ◽  
Manor Sigal ◽  
...  

Abstract More than 800 children with acute lymphoblastic leukaemia (ALL) are treated every year according to ALL IC-BFM 2002 protocol, which was designed by the International-BFM Group as a parallel to MRD-based ALL/AIEOP BFM 2000 study. The ALL-IC BFM 2002 risk group stratification comprises blast proportion in peripheral blood (PB) after 7 days of prednisone and one IT-MTX (prednisone response) and bone marrow (BM) morphology evaluation at days 15 and 33 of therapy together with age, initial WBC and presence of BCR/ABL and MLL/AF4 fusion. One of the aims of the ALL IC-BFM 2002 study is the comparison of this risk group assessment to the MRD-based criteria used in ALL-BFM 2000. We analyzed a total of 203 patients treated according to the ALL IC-BFM 2002 in the Czech Republic, Israel, Hong Kong and Uruguay for the presence of clonal antigen receptor rearrangements. MRD was evaluated in 175 patients at several time-points of therapy including mandatory points at week 5 and 12, which are used in the ALL/AIEOP BFM 2000 stratification. In total, 654 follow-up BM specimens and 80 PB samples were tested. In the univariate analysis, a good molecular response defined as MRD negativity at both week 5 and 12 was associated with the age of 1–6 years (p=0.0001), WBC<20,000/mm3 (p=0.0002), non-T immunophenotype (p<0.0001), good prednisone response (p=0.0006), presence of TEL/AML1 fusion (p=0.003) and non-M3 morphology (≤25% blasts in BM) at day 15 (p=0.02). There was no significant association of MRD negativity with sex and hyperdiploidy; non-M3 BM morphology at day 8 was significant only when analyzing non-T ALL (p=0.02). Patients with BCP ALL had significantly lower MRD levels at day 15 (p=0.03) and at day 33 (p=0.001) than T-ALL patients; the difference was no more significant at week 12. Patients stratified to standard risk group (SRG) according to the ALL IC-BFM 2002 criteria had a significantly better molecular response defined as MRD negativity at week 5 and 12 than intermediate risk group (IRG) patients (p=0.009). However, in 24 of 69 SRG patients (34.7%), MRD positivity at week 5 and/or at week 12 was observed (ranging from borderline positivity to 1.5x10(-2)), thus identifying patients who would not qualify to MRD-based SRG in ALL/AIEOP BFM 2000. Within ALL IC SRG, patients with slow molecular response did not differ significantly from those with good MRD response in age, sex, WBC, BM morphology at day 15 and presence of hyperdiploidy or TEL/AML1 fusion. The only difference was in a higher proportion of M3 BM at day 8 in MRD slow-responders (p=0.04). Our findings revealed a significant divergence between the stratification results of ALL IC-BFM 2002 and ALL-BFM 2000. A fast morphological response to treatment (M1 or M2 bone marrow at day 15) together with other low-risk features does not necessarily correspond with rapid MRD clearance. Supported by MSM0021620813, Israel Cancer Association and Children’s Cancer Foundation Hong Kong.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Stephanie L. Rellick ◽  
Gangqing Hu ◽  
Debra Piktel ◽  
Karen H. Martin ◽  
Werner J. Geldenhuys ◽  
...  

AbstractB-cell acute lymphoblastic leukemia (ALL) is characterized by accumulation of immature hematopoietic cells in the bone marrow, a well-established sanctuary site for leukemic cell survival during treatment. While standard of care treatment results in remission in most patients, a small population of patients will relapse, due to the presence of minimal residual disease (MRD) consisting of dormant, chemotherapy-resistant tumor cells. To interrogate this clinically relevant population of treatment refractory cells, we developed an in vitro cell model in which human ALL cells are grown in co-culture with human derived bone marrow stromal cells or osteoblasts. Within this co-culture, tumor cells are found in suspension, lightly attached to the top of the adherent cells, or buried under the adherent cells in a population that is phase dim (PD) by light microscopy. PD cells are dormant and chemotherapy-resistant, consistent with the population of cells that underlies MRD. In the current study, we characterized the transcriptional signature of PD cells by RNA-Seq, and these data were compared to a published expression data set derived from human MRD B-cell ALL patients. Our comparative analyses revealed that the PD cell population is markedly similar to the MRD expression patterns from the primary cells isolated from patients. We further identified genes and key signaling pathways that are common between the PD tumor cells from co-culture and patient derived MRD cells as potential therapeutic targets for future studies.


2003 ◽  
Vol 21 (20) ◽  
pp. 3853-3858 ◽  
Author(s):  
Irene Y. Cheung ◽  
M. Serena Lo Piccolo ◽  
Brian H. Kushner ◽  
Nai-Kong V. Cheung

Purpose: A promising treatment strategy for stage 4 neuroblastoma patients is the repeated application of anti-GD2 immunotherapy after activating myeloid effectors with granulocyte-macrophage colony-stimulating factor (GM-CSF). To use early marrow response as a prognostic marker is particularly relevant for patients not likely to benefit from this therapy. Patients and Methods: Eighty-six stage 4 neuroblastoma patients older than 1 year at diagnosis were classified in four clinical groups on protocol entry: complete remission or very good partial remission (n = 33), primary refractory (n = 33), secondary refractory (n = 10), and progressive disease (n = 10). Bone marrow samples collected before and following treatment were assayed for GD2 synthase mRNA by real-time reverse transcriptase polymerase chain reaction. Response and survival analyses were performed on posttreatment samples before the third cycle at 1.8 months from protocol entry. Results: GD2 synthase mRNA was evident in pretreatment marrow samples of the four clinical groups (42%, 52%, 60%, and 80% of samples, respectively), with median transcript level of 10.0, 16.6, 26.5, and 87.2, respectively. This marker became negative following antibody plus GM-CSF in 77% of complete remission or very good partial remission, 45% of primary refractory, 25% of secondary refractory, and 0% of progressive disease group. Progression-free survival was statistically different between responder and nonresponder groups (P < .0001). Among patients with minimal residual disease, molecular responders had a significantly lower risk of disease progression at a median follow-up of 29.8 months (P = .0001). Conclusion: GD2 synthase mRNA is a sensitive response marker of neuroblastoma in the bone marrow. It is particularly useful for minimal residual disease evaluation and may potentially be useful as an early predictor of resistance to antibody plus GM-CSF immunotherapy.


Blood ◽  
2008 ◽  
Vol 111 (6) ◽  
pp. 2984-2990 ◽  
Author(s):  
Stella M. Davies ◽  
Michael J. Borowitz ◽  
Gary L. Rosner ◽  
Kristin Ritz ◽  
Meenakshi Devidas ◽  
...  

Abstract Minimal residual disease (MRD) as a marker of antileukemic drug efficacy is being used to assess risk status and, in some cases, to adjust the intensity of therapy. Within known prognostic categories, the determinants of MRD are not known. We measured MRD by flow cytometry at day 8 (in blood) and at day 28 (in bone marrow) of induction therapy in more than 1000 children enrolled in Pediatric Oncology Group therapy protocols 9904, 9905, and 9906. We classified patients as “best risk” if they had cleared MRD by day 8 of therapy and as “worst risk” if they had MRD remaining in bone marrow at day 28, and tested whether MRD was related to polymorphisms in 16 loci in genes hypothesized to influence response to therapy in acute lymphoblastic leukemia (ALL). After adjusting for known prognostic features such as presence of the TEL-AML1 rearrangement, National Cancer Institute (NCI) risk status, ploidy, and race, the G allele of a common polymorphism in chemokine receptor 5 (CCR5) was associated with more favorable MRD status than the A allele (P = .009, logistic regression), when comparing “best” and “worst” risk groups. These data are consistent with growing evidence that both acquired and host genetics influence response to cancer therapy.


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