scholarly journals Prolonged Response of a Patient with Relapsed Acute Myeloid Leukemia to a Novel Oral Bromodomain Extraterminal Inhibitor (BETi)

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Meilen Chang Muñoz ◽  
Jennifer A. Murphy ◽  
Johannes E. Wolff ◽  
Brian A. Jonas

Acute myeloid leukemia (AML) is an aggressive clonal bone marrow cancer characterized by high rates of relapse and mortality. A middle-aged woman with AML relapsed twice after achieving complete remission with induction therapy and subsequent salvage therapy. She was then enrolled in a clinical trial with the bromodomain extraterminal inhibitor (BETi) mivebresib and achieved complete remission with incomplete count recovery (CRi) with monotherapy. Subsequently, she relapsed and was transitioned to combination therapy with mivebresib plus venetoclax and achieved CR again. The patient required eltrombopag to decrease platelet dependence in both arms of the trial and exhibited less myelosuppression with the combination therapy. The exceptional response to mivebresib demonstrated by this patient underscores the therapeutic potential of mivebresib.

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Pankit Vachhani ◽  
Prithviraj Bose

Myeloid sarcoma represents the proliferation of myeloblasts of acute myeloid leukemia (AML) at extramedullary sites. While extramedullary involvement in AML is uncommon in itself, isolated myeloid sarcomas, that is, myeloid sarcomas without any bone marrow involvement, are extremely rare and pose a diagnostic and therapeutic challenge. Here, we present the case of a middle-aged woman with isolated myeloid sarcoma in the stomach—an organ seldom involved by this disease. Additionally, the literature on the epidemiology, diagnosis, pathology, prognosis, and therapeutic options in myeloid sarcomas has been reviewed.


2020 ◽  
Vol 11 (9) ◽  
Author(s):  
Kai Chen ◽  
Qianying Yang ◽  
Jie Zha ◽  
Manman Deng ◽  
Yong Zhou ◽  
...  

Abstract Acute myeloid leukemia (AML) is a heterogeneous myeloid neoplasm with poor clinical outcome, despite the great progress in treatment in recent years. The selective Bcl-2 inhibitor venetoclax (ABT-199) in combination therapy has been approved for the treatment of newly diagnosed AML patients who are ineligible for intensive chemotherapy, but resistance can be acquired through the upregulation of alternative antiapoptotic proteins. Here, we reported that a newly emerged histone deacetylase inhibitor, chidamide (CS055), at low-cytotoxicity dose enhanced the anti-AML activity of ABT-199, while sparing normal hematopoietic progenitor cells. Moreover, we also found that chidamide showed a superior resensitization effect than romidepsin in potentiation of ABT-199 lethality. Inhibition of multiple HDACs rather than some single component might be required. The combination therapy was also effective in primary AML blasts and stem/progenitor cells regardless of disease status and genetic aberrance, as well as in a patient-derived xenograft model carrying FLT3-ITD mutation. Mechanistically, CS055 promoted leukemia suppression through DNA double-strand break and altered unbalance of anti- and pro-apoptotic proteins (e.g., Mcl-1 and Bcl-xL downregulation, and Bim upregulation). Taken together, these results show the high therapeutic potential of ABT-199/CS055 combination in AML treatment, representing a potent and alternative salvage therapy for the treatment of relapsed and refractory patients with AML.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 2654-2654 ◽  
Author(s):  
Shilpan S. Shah ◽  
Hagop M Kantarjian ◽  
Farhad Ravandi ◽  
Susan O'Brien ◽  
Guillermo Garcia-Manero ◽  
...  

Abstract Background Patients with acute myeloid leukemia (AML) who achieve complete remission (CR) after frontline therapy have better outcomes in terms of relapse-free survival and overall survival than those who fail to achieve CR. Patients that achieve complete remission with incomplete platelet recovery (CRp) have an inferior outcome than those with CR, but better than those with no response (Walter et al, JCO 2010). In the setting of relapsed or refractory patients who receive salvage therapy, responses such as CRp and CR with incomplete blood count recovery (CRi) may be seen more frequently. However the clinical benefit of such responses is not known. Aim To evaluate if less-than-complete remissions (CRi) after salvage therapy impact overall survival in relapsed or refractory AML patients when compared to complete remission and no response. Methods We conducted a retrospective analysis of all patients who received salvage therapy (1st and 2nd salvage only) for relapsed or refractory AML at our institution between 2010 and 2012. To assess achievement of response, patients usually have to survive at least 4 weeks as the bone marrow assessment is done at this time. Thus, to adjust for the lead-time bias of patients who achieved any kind of response, only patients who survived at least 4 weeks from the initiation of therapy were included in the analysis. The responses were classified into 3 categories – 1. Complete remission (CR); 2. Incomplete response which includes incomplete blood count recovery (CRi), morphologically leukemia free (MLF), partial response (PR) and 3. No response. Response categories were defined according to the International Working Group response definitions (Cheson et al, 2003). Results During the observation period, 217 patients received 1st or 2nd salvage therapy. Twenty-one of these patients died before 4 weeks after initiation of treatment and were therefore excluded from this analysis. Median age of all patients was 60 years (18-86). 118 patients had received one prior therapy (i.e., 1st salvage group) while 78 had two prior therapies (i.e., 2nd salvage group). Salvage therapy for this analysis was heterogeneous and was classified into hypomethylating agent based therapy in 23 (12%) patients, high-dose cytarabine (>500mg/m2) based regimens in 133 (68%) patients and various investigational regimens in 40 (20%) patients. The last group included investigational new agents or standard agents (other than hypomethylating or cytarabine) being studied in investigational doses or combinations. Prognostic groups based on cytogenetics showed 11(6%), 25(13%), 71(36%) and 76(38%) patients had favorable, intermediate, diploid and adverse cytogenetics, respectively. In 13 (7%) patients, we had insufficient or no sample for cytogenetics. Thirty-five (18%) were FLT3-ITD positive, FLT D835 point mutation was positive in 10 (5%) patients, 2 patients had both ITD and point mutation and FLT3 status was not available in 8(4%) patients; all others were negative. After salvage therapy, 39 (20%) patients achieved CR at some point in their therapy. CRi/PR/MLF was seen in 35 (18%) patients and remaining had no response. Within the CRi/PR/MLF group, the number of patients achieving CRi, MLF and PR were 28, 6 and 1, respectively. The median survival of all patients was 28.4 weeks. Median overall survival for patients in three groups was 79 weeks, 45 weeks and 27 weeks, respectively (p<0.001). Considering only patients receiving 1st salvage therapy, the median survivals for the three groups were 45.6, 41.0 and 28.9 weeks, respectively. Corresponding values for those receiving 2nd salvage were 42.1, 28.1 and 26.7 weeks, respectively. A total of 62(31%) patients received stem cell transplant out of which 47 (24%) had received it after the salvage therapy. Three patients had received two stem cell transplants and salvage therapy was in between the two. The number of patients receiving transplant in three groups (CR, CRi and no response) were 21 (11%), 16(8%) and 13(7%), respectively. Conclusions This analysis suggests that achievement of CRi, MLF or PR in AML patients receiving 1st or 2nd salvage therapy is associated with clinical benefit manifested by improved survival. Although CR still confers the greatest benefit, lesser responses also have a significant impact in survival. Disclosures: No relevant conflicts of interest to declare.


2007 ◽  
Vol 7 (2) ◽  
pp. 431-441 ◽  
Author(s):  
Jin Young Kim ◽  
Ho-Jun Song ◽  
Hoi-Jeong Lim ◽  
Myung-Geun Shin ◽  
Jae Seong Kim ◽  
...  

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 3684-3684
Author(s):  
Abhishek Mangaonkar ◽  
Jamal Mohsin ◽  
Joshua Mansour ◽  
Ashis Mondal ◽  
Ravindra B. Kolhe ◽  
...  

Abstract Introduction: Acute myeloid leukemia (AML) affects about 3.5 per 100,000 people per year in the western world. High dose chemotherapy with anthracycline and cytarabine combination has resulted in complete remission rates of around 60% even in elderly patients. Complete remission (CR) is commonly defined as bone marrow blast count of less than 5% with recovery of all three cell lines in the peripheral blood. CR with incomplete count recovery is where there is no evidence of persistent disease but there is an incomplete recovery of blood counts, is also seen frequently and it has been shown to have poor prognosis as compared to patients with normal count recovery. Above normal platelet count is seen in small percentage of patients and the significance of this has not been well described.. We hypothesized that patients with a high platelet count at recovery from induction therapy have an increased survival as compared to those with normal or below normal platelet counts. Methods: We did a retrospective chart review of 123 consecutive patients with a diagnosis AML at Georgia Regents University Cancer Center that were admitted for induction treatment between 2005 and 2012. Highest platelet count between days 25 to 35 from the date of initiation of induction chemotherapy was taken for this analysis. Patients were divided into three groups: platelet count <50,000 (n=21); 50,000-400,000 (n=80) & >400,000 (n=22). Stratified survival with Kaplan-Meir curves were calculated for each of the groups. Results: Mean follow-up period was 94.122 months and median survival was 33.917 months. Mean survival (in months) for the first group was 23.157; 57.801 for the second group & 187.388 for the third group. Difference between survival curves was statistically significant (p=0.003). Conclusion: Patients with complete remission appear to have significant survival advantage as compared to those with incomplete platelet recovery. Review of patients across various large clinical trials from US showed that the patients with CR have 3-5 year survival advantage as compared to those with incomplete platelet recovery. Platelet count at the end of one month after initiation of induction chemotherapy can also be used to predict long-term prognosis. This observation would serve as a valuable addition to the already established prognostic markers such as cytogenetics and molecular studies. Our results need to be validated in a larger set of patients. Disclosures Kolhe: Georgia Regents University: LLS grant Other, Research Funding. Jillella:Emory University: Research Funding. Kota:Georgia Regents University: LLS grant Other, Research Funding; Emory University: Advisory board, Ponatinib, Advisory board, Ponatinib Other; Teva: Speakers Bureau.


2017 ◽  
Vol 6 (2) ◽  
pp. 271-275 ◽  
Author(s):  
Seyed Mehdi Hashemi ◽  
Shokoufeh Mahmoudi Shan ◽  
Mahdi Jahantigh ◽  
Abolghasem Allahyari

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 4650-4650
Author(s):  
Andrew James Innes ◽  
Philippa Woolley ◽  
Richard Szydlo ◽  
Sara Lozano ◽  
Fiona Fernando ◽  
...  

Abstract Background: For the majority of patients with acute myeloid leukemia (AML), allogeneic hematopoietic cell transplantation (HCT) offers the best prospect of long-term survival. However both the risk of relapse and non-relapse mortality remain stubborn barriers to successful outcome. Remission status is one of the strongest predictors of outcome, and while conventional risk stratification models account for this, complete remission with incomplete count recovery (CRi) is typically ascribed the same predictive value as complete remission (CR). Methods: In this single center retrospective study we assessed the impact of incomplete count recovery on outcome of allogeneic HCT for AML. Patients' disease status was classified immediately prior to HCT as complete remission (CR), complete remission with incomplete count recovery (CRi) or no complete remission (no CR/CRi). The conventional definition of complete remission (&lt;5% marrow blasts by morphology) was employed and incomplete count recovery was defined as platelet count &lt;100 x 109/L and/or absolute neutrophil count &lt; 1 x 109/L. Measurable residual disease (MRD) was defined by detectable disease by a contemporaneously accepted standard methodology at the time of transplant (e.g. PCR or immunophenotyping). The primary outcome measure was overall survival, and secondary endpoint of non-relapse mortality and relapse were also assessed. Results: Between January 2005 and December 2017, 155 patients underwent allogeneic HCT for AML in our institution. Disease status was defined as CR in 82 (53%), CRi in 54 (35%) and no CR/CRi in 19 (12%). No significant demographic or transplant characteristics were observed between the groups. With a median follow-up of 3.4 [0.1 - 12.8] years, survival at 3 years was 42.5% for the whole cohort with significant differences between the three groups: 54.3% for CR, 34.8% for CRi and 13.4% for no CR/CRi (p&lt;0.001; fig 1A; HR 1.94 for CRi, and 3.4 for no CR). These differences remained after corrections for standard transplant risk factors. The significant differences in overall survival between CR and CRi groups were accounted for by increased non-relapse mortality (7.5% vs. 24.2% at 100 days and 28.7 vs 44.9% at 3 years (p=0.003), fig 1B). The overall cumulative incidence (CI) of relapse at 3 years was 32.4%, and while those patients transplanted not in CR/CRi has a significantly increased CI of relapse (55.3%, p=0.006), there were no significant differences between the CR and CRi groups (25.1 and 36.7% respectively (p=0.441; fig 1C). Patients without MRD (n=107) had a lower incidence of relapse compared to those with MRD (n=48, 21.9% vs. 48.1%, p=0.009), however MRD negative patients with incomplete recovery still had a significantly worse 3-year survival than those with complete recovery (37.5 vs 56.7, p=0.006) resulting from higher NRM (46.4% vs 30.4%%, p=0.003, fig 1D). Discussion: CRi patients have a poorer survival and higher NRM than CR patients with full marrow recovery, without evidence of increased relapse. While death from NRM is a competing risk for relapse, the increased incidence of relapse remains overtly demonstrable in those patients transplanted not in CR/CRi, despite an equally high NRM. Additionally, the persistently increased NRM in CRi patients without MRD, suggests that the poorer survival may result from poor fitness for transplant and increased susceptibility to transplant related complications rather than an imminent relapse. With the advent of increasingly sensitive MRD technologies, these data may suggest that further pre-transplant optimization to promote marrow recovery may be permissible in order to minimize NRM without risking increased risk of relapse in CRi patients. Figure 1. Figure 1. Disclosures Apperley: Pfizer: Honoraria, Speakers Bureau; BMS: Honoraria, Speakers Bureau; Novartis: Honoraria, Research Funding, Speakers Bureau; Incyte: Honoraria, Speakers Bureau.


Blood ◽  
2012 ◽  
Vol 119 (17) ◽  
pp. 3917-3924 ◽  
Author(s):  
Geoffrey L. Uy ◽  
Michael P. Rettig ◽  
Ibraheem H. Motabi ◽  
Kyle McFarland ◽  
Kathryn M. Trinkaus ◽  
...  

Abstract The interaction of acute myeloid leukemia (AML) blasts with the leukemic microenvironment is postulated to be an important mediator of resistance to chemotherapy and disease relapse. We hypothesized that inhibition of the CXCR4/CXCL12 axis by the small molecule inhibitor, plerixafor, would disrupt the interaction of leukemic blasts with the environment and increase the sensitivity of AML blasts to chemotherapy. In this phase 1/2 study, 52 patients with relapsed or refractory AML were treated with plerixafor in combination with mitoxantrone, etoposide, and cytarabine. In phase 1, plerixafor was escalated to a maximum of 0.24 mg/kg/d without any dose-limiting toxicities. In phase 2, 46 patients were treated with plerixafor 0.24 mg/kg/d in combination with chemotherapy with an overall complete remission and complete remission with incomplete blood count recovery rate (CR + CRi) of 46%. Correlative studies demonstrated a 2-fold mobilization in leukemic blasts into the peripheral circulation. No evidence of symptomatic hyperleukocytosis or delayed count recovery was observed with the addition of plerixafor. We conclude that the addition of plerixafor to cytotoxic chemotherapy is feasible in AML, and results in encouraging rates of remission with correlative studies demonstrating in vivo evidence of disruption of the CXCR4/CXCL12 axis. This study was registered at www.clinicaltrials.gov, no. NCT00512252.


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