scholarly journals HIGH INFECTION RELATED MORTALITY IN PAKISTANI CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKAEMIA DURING REMISSION INDUCTION CHEMOTHERAPY: REVIEW OF DATA FROM A SINGLE INSTITUTION

2016 ◽  
Vol 2 (4) ◽  
Author(s):  
AUR Maaz ◽  
Farhana Badar ◽  
Tariq Mahmood ◽  
Ibrahim Al Nassir

Purpose: Despite advances in the treatment of acute lymphoblastic leukaemia (A.L.L.), the outcome for children living in the developing countries is still poor. This is in large part due to high treatment-related mortality (TRM). This study was carried out to review the data and analyze the factors resulting in high TRM during remission induction chemotherapy. Methods: Data for children treated at our centre during the calendar year 2007 were retrospectively analysed. Standard four-drug induction chemotherapy was used without risk strati cation. Bone marrow evaluation was carried out at days 8 and 28. Cerebrospinal uid analysis was carried out on day 1 and with each subsequent intrathecal chemotherapy injection. Modern supportive care facilities including antibiotics, nutritional support and intensive care unit were available. Results: Eighty-one children were eligible for analysis. Median age was 5 years (range 2–16), 72% were male with M:F ratio of 2.5:1. Seventy- five (92%) children had precursor B-cell A.L.L. Only 2 children had central nervous system leukaemia at presentation. Median presenting white blood cell count was 8.83 (range: 1–446). Severe malnutrition (weight <5th centile for age) was seen in 42% of children. Median symptom duration was 6 (range 1–30) weeks at the time of presentation. Induction mortality was 25%. Induction mortality was 25.6% (n = 21). Twenty were related to infections, while more than half (52%) occurred as a result of an outbreak of Acinetobacter infection. Severe malnutrition and Acinetobacter infection (due to an outbreak in our unit during the study period) were highly predictive of TRM during remission induction chemotherapy. Conclusions: Infection control measures, health education and reduction in treatment intensity may improve survival for children with A.L.L. in Pakistani population. Key words: Acute lymphoblastic leukaemia in children, malnutrition, Pakistan, treatment-related mortality

2010 ◽  
Vol 56 (4) ◽  
pp. 551-559 ◽  
Author(s):  
Bendik Lund ◽  
Ann Åsberg ◽  
Mats Heyman ◽  
Jukka Kanerva ◽  
Arja Harila-Saari ◽  
...  

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 3750-3750
Author(s):  
Bryan Brinda ◽  
Viet Q. Ho ◽  
Timothy George ◽  
Jeffrey E Lancet ◽  
Rami S. Komrokji

Abstract Background: The median age of diagnosis for acute myeloid leukemia (AML) is between age 65 and 70. While advances in therapy and supportive care in the past several decades has significantly improved outcomes in younger patients, the prognosis in elderly AML patients, defined as age 60 or greater, remains dismal. In addition, many elderly patients are unable to receive such aggressive therapy due to increased treatment-related mortality and poorer clinical response. There remains great interest in identifying factors that are associated with both beneficial and detrimental outcomes in this patient population. Methods: This was a retrospective analysis conducted at Moffitt Cancer Center. The primary study objective was to compare the incidence of 30-day mortality of patients aged 60-69 years vs. patients 70 years or older with newly diagnosed AML who received intensive remission induction chemotherapy. Secondary endpoints included 60-day mortality, overall survival (OS), complete response rate (CR), receipt of allogeneic hematopoietic stem cell transplant, rate of infection, cardiac complications, major organ failure, ICU transfer, and any other treatment-related complications. Baseline patient characteristics at diagnosis were summarized using descriptive statistics including mean, median, standard deviation, and range for continuous measures and proportions and frequencies for categorical measures. The primary outcome was assessed via chi-squared analysis. Assuming treatment-related mortality is 5% in the younger patients and 15% in patients > 70 years old, with a 2-sided p-value of 0.05, a sample size of 300 would provide a power of 0.83 to detect this 10% difference in mortality. Overall survival was estimated using the Kaplan-Meier method, and compared using a log-rank test. Univariate and multivariate analyses using Cox-Regression models were conducted to identify factors affecting OS. Results: A total of 246 patients with newly diagnosed AML between age 60-69 (n=132) and 70 or greater (n=114) who underwent initial remission-induction chemotherapy between July 2009 and July 2014 were identified and included in this analysis. Background characteristics and known factors that affect CR and OS such as overall risk category and performance status were well matched between groups. Sixty-four (56%) patients in the older and 62 (47%) patients in the younger group received 7+3 induction chemotherapy, whereas 41 (36%) in the older and 50 (38%) in the younger group received cladribine-based regimens. The remainder of patients received clinical trial induction chemotherapy. Twenty-three (17.4%) of patients in the younger patient group underwent immediate re-induction chemotherapy, compared to 8 (7%) patients in the older group (p=0.02). Thirty day mortality rate was 6.8% (9) in the younger group and 14% (16) in the older group (p=0.062). By day 60 after initiation of induction chemotherapy, 13.6% (18) and 23.7% (27) of patients in the younger and older cohorts, respectively, were deceased (p=0.031). No difference was noted in infection rate, ICU transfer, major organ failure, percentage of patients intubated, incidence of tumor lysis syndrome, or initiation of parenteral nutrition. Seventy-nine (59.8%) patients in the younger arm achieved CR, compared to 51 (44.7%) patients in the older arm (p=0.003). Median OS was 10.4 months and 8.3 months in the younger and older group respectively (p=0.002). Significantly more patients in the younger group went on to receive stem cell transplant. Multivariate analysis of the composite group revealed age >75, risk category, prior therapy with hypomethylating agents, and number of comorbidities were predictors of poorer survival. Conclusions: The presented study demonstrates that intensively-treated patients age ≥70 have an increased early treatment-related mortality, similar treatment-related morbidity, and a lower incidence of CR and OS compared to patients age 60-69. Additionally, prior hypomethylator use, risk category and comorbidities contribute to poorer survival. These observations give further insight into the role of intensive remission chemotherapy in an elderly AML patient population. Table 1. Multivariable Analysis Overall Survival (p = <0.05) Hazard Ratio 95% CI Age >75 1.5 1.06-2.20 Risk Category 1.1 1.01-1.16 Prior Hypomethylator 1.6 1.17-2.12 No. of Comorbidities 1.1 1.04-1.20 Disclosures Off Label Use: Cladribine for use in acute myeloid leukemia.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 3290-3290
Author(s):  
Muthalagu Ramanathan ◽  
Zheng Zhou ◽  
Jan Cerny ◽  
Glen D Raffel ◽  
Laura Petrillo-Deluca ◽  
...  

Abstract Abstract 3290 Background: Patients with high risk AML, defined as those with age > 60 years or multiple medical co-morbidities determined by Charleston comorbidity index (CCI) carry a poor prognosis and inferior outcomes after 7+3 induction chemotherapy. CR rates tend to range from 6–51% and induction death rates between 9–48%. We present here a single institution experience of high risk AML patients treated with an induction regimen consisting of high dose mitoxantrone and cytarabine (HiDAC/MITO). Methods: We performed a retrospective analysis of all patients with AML who received HiDAC/MITO induction from January 2009- January 2010 at our institution. Patients with age ≥60 or age <60 with high CCI received HiDAC at 3gm/m2 over three hours on days 1 to 5 plus MITO 80mg/m2 once on day 2. Effect of other high risk features including poor risk cytogenetics, therapy related AML (t-AML), AML with prior antecedent hematological disorder (AHD) and relapsed AML on treatment outcome were also evaluated. The primary endpoints of the study were CR (defined as bone marrow blasts <5%) at day 30 and treatment related mortality within 30 days of initiation of treatment. End of follow-up was June 30, 2010. Results: 20 AML had received HiDAC/MITO for remission induction. The median age was 66.5 years (range 47 to 78), those with age ≥ 70 was 8 (40%). CCI was ≥ 5 in 18 (90%) patients. Other high risk features included high risk cytogenetics in 8 (40%) and non-denovo AML (AML with AHD, t-AML or relapsed AML) in 11 (55%). Overall CR rate was 17 (85%, CI: 61%-96%) and 3 (15%) patients had refractory disease. There was no treatment related mortality. Median time to neutrophil recovery (>1000/ul) was 27 (range 19 to 37) days and median time to platelet recovery (>100,000/ul) was 28 days (range 23 to 44) days. Patients with non–denovo AML were more likely to be refractory to treatment or relapse after day 30. Median follow up of the entire cohort is 288 (range 29 to 530) days. 3 month and 6 month overall survival (OS) was 94.7% and 73.3% and progression free survival (PFS) 93.8% and 87.5%, respectively. The median OS was 410 days (CI: 243-*); (denovo 410 vs. others 381 days). Median PFS is 524 days (CI: 381-*); (denovo *not reached vs. others 381 days). 11(55%) patients were able to proceed to autologous (4) or allogeneic (7) stem cell transplantation (SCT) after receiving HiDAC/MITO. The time to transplant ranged from 44 to 195 days. Median OS of the patients who underwent SCT is 524 days versus 269 days for the non transplant group (p =0.0038). The HiDAC/MITO induction regimen was well tolerated. Cardiac toxicity defined by symptomatic CHF was noted in 6/20 patients. Of the six patients 2 had prior cardiac history and 1 had prior anthracycline exposure and 1 had both anthracycline exposure and cardiac history. Cardiac toxicity was delayed and identified by echo at a median of 90 range (42 to139) days after induction chemotherapy. None of these patients died from cardiac toxicity. Conclusions: In this high risk AML population, HiDAC/MITO induction was well tolerated and demonstrated an overall response rate of 85% and no induction deaths, allowing a substantial number (55%) of patients to proceed to SCT. Contrary to our expectations advanced age or multiple medical co-morbidities did not affect CR rate or survival, thus high lighting the utility of this regimen for high risk newly diagnosed elderly patients with AML. Disclosures: No relevant conflicts of interest to declare.


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