scholarly journals Venetoclax with decitabine vs intensive chemotherapy in acute myeloid leukemia: A propensity score matched analysis stratified by risk of treatment‐related mortality

Author(s):  
Abhishek Maiti ◽  
Wei Qiao ◽  
Koji Sasaki ◽  
Farhad Ravandi ◽  
Tapan M. Kadia ◽  
...  
Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 2277-2277
Author(s):  
Colin Godwin ◽  
Megan Othus ◽  
Vicky Sandhu ◽  
Elihu H. Estey ◽  
Roland B. Walter

Abstract Introduction Despite improvements in supportive care, treatment-related mortality (TRM) remains a significant problem for patients with acute myeloid leukemia (AML). In order to quantify fitness for intensive AML therapies, we recently developed a multivariate model for predicting TRM, defined as death within 28 days of treatment initiation in patients undergoing intensive induction chemotherapy for newly-diagnosed AML. Here, we examine the performance of this TRM model in patients with relapsed or refractory AML and assess whether the model can be improved for this population. Methods Using a database of patients treated for AML at our institution since 2003, we identified patients with relapsed or refractory disease treated with intensive chemotherapy, defined as regimens that were at least as intense as typical “7+3” regimens; patients who received treatment protocols with cytarabine <100 mg/m2/day or demethylating agents alone were excluded. We collected the following variables required to calculate the TRM score: ECOG performance status, age, platelet count, albumin, presence or absence of secondary AML, WBC, peripheral blood blast percentage, and creatinine. TRM scores were then calculated as described in J Clin Oncol 2011;29:4417. For a subset of these patients, the following additional variables were collected: duration of prior complete remission, number of prior chemotherapy regimens, number of prior hematopoietic cell transplants, and the number of antibiotics prescribed for treatment of presumed or documented infections at the time of chemotherapy initiation. For this smaller subset, we used a logistic regression model to create a preliminary updated TRM model that included these clinical variables in addition to the variables in the original TRM score. Finally, we used the area under the receiver operator characteristic curve (AUC) to quantify the ability of a model to predict TRM; in this approach, an AUC of 1 indicates perfect prediction of TRM while an AUC of 0.5 indicates no prediction; AUC values of 0.6-0.7, 0.7-0.8, and 0.8-0.9 are commonly considered as poor, fair, and good, respectively. Results A total of 270 patients met our study inclusion criteria. Fifteen (5.6%) died within 28 days of starting chemotherapy, i.e. experienced TRM. The AUC for the previously published TRM score in predicting early death in this population was 0.66. For comparison, in our original study of 2,238 patients with newly-diagnosed AML, we obtained an AUC of 0.82. Expanding the definition of TRM to include those patients who died within 60 (N = 47, 17.4%) or 90 days (N = 75, 27.8%) of starting chemotherapy did not improve the original model’s performance in our cohort (AUCs of 0.62 and 0.59, respectively). The additional variables described above were available for 133 of the 270 patients in our cohort. Within this subset, the AUC for the original TRM score was 0.65 in predicting death within 28 days. Incorporation of these new covariates in a preliminary TRM model yielded an improved AUC of 0.81 for this smaller subset. Conclusions Our data indicate that the TRM score, originally developed for patients with newly-diagnosed AML, only has a fair ability to predict TRM in patients with relapsed and refractory AML. However, with inclusion of additional covariates, such as prior CR duration and number of prior chemotherapies, TRM can be predicted quite well, to a degree similar to the accuracy demonstrated by the original model in newly-diagnosed patients. While our findings need to be confirmed in larger, independent cohorts of patients, they suggest the possibility of developing an objective measure to determine fitness for intensive salvage chemotherapy in AML. Disclosures No relevant conflicts of interest to declare.


2020 ◽  
Vol 25 (4) ◽  
pp. 288-294
Author(s):  
Tariq Ghafoor ◽  
Shakeel Ahmed ◽  
Sumaira Khalil ◽  
Tanzeela Farah

OBJECTIVES Treatment outcome in children with acute myeloid leukemia (AML) has improved in the developed world but remains poor in developing countries. We assessed the role of etoposide in induction chemotherapy in pediatric AML. METHODS This analysis retrospectively compared 2 induction chemotherapy regimens consisting of daunorubicin and cytarabine with etoposide (ADE) and without etoposide (AD). All newly diagnosed cases of AML younger than 18 years from January 1, 2012, onwards who completed their treatment before January 31, 2019, were included. Data of 186 cases, including 117 males (62.9%) and 69 females (37.1%), were analyzed. Demographic, initial presentation blood counts, and AML subtypes were almost identical in both groups. RESULTS Complete remission rates were almost identical for the ADE versus the AD group (78.8% vs 80.0%, p = 0.980). Treatment-related mortality was higher, albeit not significantly, in the ADE (25 of 105; 23.8%) versus the AD (16 of 81; 19.8%) group (p = 0.508). Overall survival was 32 of 105 (30.5%) in the ADE and 43 of 81 (53.1%) in the AD group (p = 0.079), and disease-free survival was 29 of 105 (27.6%) and 39 of 81 (48.1%) in ADE and AD groups (p = 0.056), respectively. CONCLUSIONS Etoposide in induction treatment of pediatric AML is associated with increased episodes of bacterial and fungal infections and high treatment-related mortality. Moreover, it does not offer any survival benefit. In low- and middle-income countries like Pakistan, it should not be used in the induction treatment protocol.


2004 ◽  
Vol 22 (21) ◽  
pp. 4384-4393 ◽  
Author(s):  
Ursula Creutzig ◽  
Martin Zimmermann ◽  
Dirk Reinhardt ◽  
Michael Dworzak ◽  
Jan Stary ◽  
...  

Purpose The rates of early death (ED) and treatment-related mortality (TRM) are unacceptably high in children undergoing intensive chemotherapy for acute myeloid leukemia (AML). Better strategies of supportive care might help to improve overall survival in these children. Patients and Methods In a retrospective study, we analyzed incidence, clinical features, and risk factors for lethal complications of 901 children enrolled onto the multicenter trials Acute Myeloid Leukemia-Berlin-Frankfurt-Muenster (AML-BFM) 93 and AML-BFM 98. Results One hundred four patients (11.5%) enrolled onto the clinical trials AML-BFM 93 and AML-BFM 98 died shortly after diagnosis or as a result of treatment-related complications. Thirty-two patients (3.5%) died before (six patients) or during (26 patients) the first 14 days of treatment, mainly as a result of bleeding or leukostasis. Low performance status, hyperleukocytosis, and French-American-British type M5 were the main risk factors for a lethal event before day 15. After day 15, the predominant causes of death were complications caused by infections, particularly bacterial and fungal infections. The incidence of lethal infections was highest during induction therapy and decreased thereafter. When comparing both clinical trials, significantly fewer patients died within the first 6 weeks in AML-BFM 98 than in AML-BFM 93 (14 [3.5%] of 430 patients v 35 [7.4%] of 471 patients; P = .01). Conclusion To reduce the high incidence of ED and TRM in children with AML, early diagnosis and adequate treatment of complications are needed. Children with AML should be treated in specialized pediatric cancer centers only. Prophylactic and therapeutic regimens for better treatment management of bleeding disorders and infectious complications have to be assessed in future trials to ultimately improve overall survival in children with AML.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 2790-2790 ◽  
Author(s):  
Lillian Sung ◽  
Robert Gerbing ◽  
Todd A. Alonzo ◽  
Yi-Cheng Wang ◽  
Etan Orgel ◽  
...  

Abstract Background: Therapy for children with acute myeloid leukemia (AML) is intensive and treatment-related mortality (TRM) occurs in about 5 to 10% of patients. Previous data illustrated that obese children and adolescents with AML treated according to CCG 2961 were more likely to experience TRM, with HR 2.66 (95% CI 1.38-5.11; P = 0.003), when compared to middleweight patients. Since this trial, the backbone of AML chemotherapy and supportive care have changed and thus, it is unknown whether the impact of obesity persists in contemporary trials. The objective was to determine whether obesity was associated with increased TRM, reduced survival and prolonged compared to middleweight patients with AML. Methods: AAML0531 enrolled patients between August 14, 2006 and June 15, 2010. For this analysis, we included patients 0 to 18 years of age with de novo AML. Chemotherapy consisted of 5 cycles of chemotherapy and patients were randomized to receive or not receive gemtuzumab once during Induction I and Intensification II. Best allogeneic donor hematopoietic stem cell transplantation (HSCT) was recommended for those with > 15% bone marrow blasts after Induction I in those without favorable risk cytogenetics and poor risk cytogenetics irrespective of response following Induction I. Matched family donor HSCT was recommended for those with good response after Induction I with standard risk cytogenetics and an available donor. Obesity was defined using definitions from the Centers for Disease Control and Prevention (CDC). Underweight was defined as a body mass index percentile less than 5th percentile, and obese 95th percentile and greater. Categories were determined using z-scores for the weight-for-height data for those 0 to 2 years of age. All outcomes were censored at the time of HSCT. The primary outcome was TRM, defined as death as first event occurring on therapy or within 30 days of going off therapy. Cumulative incidence of TRM was estimated treating relapse and failure as competing events. Kaplan Meier analysis was conducted for overall survival (OS), event free survival (EFS), and disease free survival (DFS). Cumulative incidence of relapse rate (RR) was estimating treating deaths as competing events. Results: There were 1004 patients included. When comparing middleweight and obese patients, there was no significant difference in gender (P=0.814), white vs non-white race (P=0.116), cytogenetic risk group (all P>0.05) or MRD positivity after Induction 1 (P=0.750). The median age was higher for obese patients (12.0 vs 9.4 years; P=0.007 years) compared with middle weight patients. The proportion of patients who were Hispanic or Latino patients was higher among obese compared with middle weight patients (28% vs 17%; P=.001). Survival outcomes are shown in Table 1. When evaluating median time to neutrophil recovery, obese patients, when compared to middleweight patients, had shorter duration of neutropenia for cycles 1-3 (P<0.05). Conclusions: TRM rates continue to be higher for obese patients treated with contemporary AML protocols. Toxicity is not mediated through prolonged neutropenia. Future work should compare the rate of toxicity among obese versus non-obese patients and evaluate the impact of underweight status. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2001 ◽  
Vol 98 (3) ◽  
pp. 565-572 ◽  
Author(s):  
Donald Bunjes ◽  
Inga Buchmann ◽  
Christian Duncker ◽  
Ulrike Seitz ◽  
Jörg Kotzerke ◽  
...  

Abstract The conditioning regimen prior to stem cell transplantation in 36 patients with high-risk acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) was intensified by treating patients with a rhenium 188–labeled anti-CD66 monoclonal antibody. Dosimetry was performed prior to therapy, and a favorable dosimetry was observed in all cases. Radioimmunotherapy with the labeled antibody provided a mean of 15.3 Gy of additional radiation to the marrow; the kidney was the normal organ receiving the highest dose of supplemental radiation (mean 7.4 Gy). Radioimmunotherapy was followed by standard full-dose conditioning with total body irradiation (12 Gy) or busulfan and high-dose cyclophosphamide with or without thiotepa. Patients subsequently received a T-cell–depleted allogeneic graft from a HLA-identical family donor (n = 15) or an alternative donor (n = 17). In 4 patients without an allogeneic donor, an unmanipulated autologous graft was used. Infusion-related toxicity due to the labeled antibody was minimal, and no increase in treatment-related mortality due to the radioimmunoconjugate was observed. Day +30 and day +100 mortalities were 3% and 6%, respectively, and after a median follow-up of 18 months treatment-related mortality was 22%. Late renal toxicity was observed in 17% of patients. The relapse rate of 15 patients undergoing transplantation in first CR (complete remission) or second CR was 20%; 21 patients not in remission at the time of transplantation had a 30% relapse rate.


Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 3-4
Author(s):  
Mecneide Mendes Lins ◽  
Juliana Teixeira Costa ◽  
Alayde Vieira Wanderley ◽  
Adriana Seber ◽  
Cinthya Rocha ◽  
...  

Introduction: Children with newly diagnosed acute myeloid leukemia (AML) may have a high early mortality when resources are limited by infrastructure or by a widespread worldwide crisis, as being faced with the SARS-Cov-2 pandemic. Many elective treatments were postponed, but newly diagnosed AML is a life-threatening disease that needs prompt therapy. With acute shortage of infra-structure as intensive care unit beds, blood supply, medication, healthcare personnel, an optimal therapy must balance anti-neoplastic efficacy and the chance of treatment-related mortality. The induction chemotherapy of pediatric patients with AML living in low- and middle-income countries has been thoroughly discussed because early mortality remains 10%-20%, much higher than in developed counties. Mild treatment schemas have been used in Japan, China and Latin America with impressive results, comparable to other intensive induction regimens. Our objective is to describe the results of this mild induction regimen used in Brazil to treat children simultaneously diagnosed with AML and Covid-19 infections. Methods: This is a retrospective multicentric trial including Brazilian children diagnosed with AML, also found to have a positive nasal and oropharyngeal PCR for SARS-Cov-2 and uniformly treated with mild induction protocol ("MAG") that included Mitoxantrone at 5 mg/m2, by i.v. infusion over 4 to 6 hours once a day on days 1, 3, and 5 (three doses in total), Cytarabine at 10 mg/m2, subcutaneous (s.c.), q 12 h for 10 days (20 doses in total) and G-CSF 5 𝜇g/kg, s.c., once a day for 10 days (10 doses in total) [Bansal D, et al. Pediatr Blood Cancer. 2019 Nov 27:e28087]. Results: From March 15 to July 1, 2020, nine children from four different institutions were diagnosed with AML (Table 1). Their median age was 9 years (range, 5 to 18), 6 female gender, all but one diagnosed with Covid-19 by nasal PCR; one had typical chest CT and positive IgM. The institutions had previously agreed on following the same induction when treating AML children infected by the SARS-Cov-2. Five of the nine had severe illness, three of them needed mechanical ventilation and one did not need supplementary oxygen despite radiologically diagnosed pneumonia. Two children had mild symptoms and two were completely asymptomatic. All children tolerated MAG chemotherapy. Neutropenia lasted for a median of 29 days (17-33) and none of them had neither thrombotic complications nor acute renal failure. All children recovered from the Covid-19 infection and 8 of 9 already evaluable children achieved complete remission of the leukemia with MRD 0-1% after the two planned cycles. All patients are alive, on therapy. Table 1: Patients characteristics Pt#AgeGenderAML-FABMolecular BiologyCytogeneticsCNS diseaseSeverelly IllDuration of Neutropenia (days)Response to 1st InductionResponse to 2nd InductionCOVID SymptomsOxygen TherapyCOVID TreatmentStatus19MM0NegativeComplex karyotype with del11NoNo330% blastsMRD 0,12%NoneNoAAlive28FM2Negativet(10,11)NoYes261% blastsToo earlyInflamatory syndromeMechanical VentilationA,C,IVIGAlive317FNOSNegativeNormalNoYes227% blastsMRD 1%PneumoniaMechanical VentilationA,I,O,C,HAlive45MM4EoInv16Inv. 16NoYes222% blastsMRD negativeMildNo-Alive58MM2Amltot(8;21)YesYes190%MRD negativeNoneNoAAlive68FNOSNot doneNot doneNoNo254% blastsMRD negativePneumoniaNoA,O,CAlive710FNOSNot doneTrisomy 22NoYes17Too earlyToo earlyPneumonia, Respiratory DistressMechanical VentilationA,O,C, IVIGAlive810FM5ASXL1NormalNoNo310%Too earlyNoneNoA,I,CiproAlive918FM2NegativeNot doneNoNo270%MRD negativeMildNoAAlive A - Azythromycin; I - Ivermectin; C - Corticosteroids, O - Oseltamivir; IVIG - Immunoglobulin; H- Heparin; Cipro- Coprofloxacin Conclusions: Against all odds, MAG was well tolerated in children and adolescents newly diagnosed with AML and active Covid-19, with no treatment-related mortality. All evaluable patients achieved remission and are currently proceeding therapy. The high prevalence of Covid-19 in our country may have to be taken into account in all oncological treatment strategies. With a shorter duration of neutropenia, the absence of mucositis or invasive fungal infections, MAG may be implemented in low- and middle-income countries as an optimal strategy to overcome induction mortality and improve outcome of children and adolescents with AML. Disclosures No relevant conflicts of interest to declare.


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