Major hemorrhage in children with idiopathic thrombocytopenic purpura: Immediate response to therapy and long-term outcome

1998 ◽  
Vol 133 (3) ◽  
pp. 334-339 ◽  
Author(s):  
Desiree Medeiros ◽  
George R. Buchanan
2004 ◽  
Vol 26 (11) ◽  
pp. 724-726 ◽  
Author(s):  
Somasundaram Jayabose ◽  
Oya Levendoglu-Tugal ◽  
Mehmet F. Ozkaynkak ◽  
Paul Visintainer ◽  
Claudio Sandoval

2004 ◽  
Vol 75 (2) ◽  
pp. 117-118 ◽  
Author(s):  
K. Ma?lanka ◽  
A. Sikorska ◽  
A. Misiak ◽  
L. Konopka ◽  
B. ?upa?ska

2017 ◽  
Vol 95 (1) ◽  
pp. 36-44
Author(s):  
Marina I. Savel’eva ◽  
A. V. Kryukov

The achievement of early cytogenetic and molecular responses is the major objective of therapy and a main prerequisite for the favourable long-term outcome of the disease. The maintenance of dose intensity and management of adverse events are keys to successful treatment of chronic myeloid leukemia (CML) with imatinib. Therapeutic monitoring and testing the drug level in blood are the efficient tools for the treatment ofpatients with CML and can be usedfor analysis of treatment failure or suboptimal response to therapy, suspected noncompliance, drug interactions or unexpected adverse reactions.


Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 3259-3259
Author(s):  
Bor-Sheng Ko ◽  
Grace Hui-Min Wu ◽  
Yu-Chiao Wang ◽  
Ming Yao ◽  
Churn-Shiouh Gau ◽  
...  

Abstract Background and Objectives Immune thrombocytopenic purpura (ITP) is a rare disease, and the epidemiology and long-term outcome are still rarely characterized. This study is then aimed to provide a population-based assessment for the demographics and outcome about ITP in Taiwan, an island in Southeastern Asia with around 23 million inhabitants. Material and Methods This study used claims data from Taiwan's National Health Insurance Research Database (NHIRD). The database included information from a nationwide, mandatory-enrollment and single-payer healthcare system with more than 99% coverage rate in Taiwan since March, 1995. To address adequate medical history tracking and outcome follow-up, only those patients with the first ITP diagnosis from Jan 1st, 2001 to Dec 31st, 2012 were included. Incident ITP was identified first with ICD-9 codes; but those cases with codes for potential ITP-confounding diseases within 6 months from the first ITP code were excluded. Next, only those patients with meaningful pharmacological treatment or splenectomy within 3 months were included in the final analysis. Chronic ITP was defined for those with ICD-9 ITP codes and continuous drug exposure for more than 3 months, or with rituximab or splenectomy. Sex- and age-matched cohorts with 1:10 ratio were selected from Taiwan general population for survival comparison. Results Of the 30673 patients with ITP codes from Jan 1st, 2001 to Dec 31st, 2012, 11437 were identified as incident ITP. The mean age was 42.9+/-27.5 y/o, and 5445 (47.6%) cases had Charlson Comorbidity Index (CCI) score more than 2. The average incidence was 4.16 per 100,000 person-year, and the details are shown in Table 1. The incidence for female was higher than that for male (4.97 vs. 3.38 per 100,000 person-year), and the incidences across the age represented a U-shape distribution, with the highest ones in those aged 0-9 y/o and more than 70 y/o (7.21 and 13.3 per 100,000 person-year, respectively). Some geographic distribution of the incidences existed, with the highest in central part and the lowest in Eastern part of Taiwan (5.33 and 2.64 per 100,000 person-year, respectively). Secondary causes could be identified in 3560 (31.0%) cases, and malignant neoplasma (1743, 49.0%) were most frequently noted. Viral hepatitis B or C were found in 785 (22.1%) cases. Chronic ITP was diagnosed during follow-up in 29.1% (n=3324) of incident ITP patients. Those incident ITP patients aged 0-9 y/o (431/2169 vs. 2893/9268, p<0.001) or male gender (1118/4697 vs. 2206/6740, p<0.001) had a less chance to develop chronic ITP. As compared with the matched cohort from general population, the 10-yr survival rate was significantly inferior for all ITP patients, no matter in those aged below 20 y/o (96.9+/-0.5% vs. 98.8+/-0.1%, p<0.0001) or above 20 y/o (62.5+/-0.8% vs. 83.2+/-0.2%, p<0.0001), as in Figure 1. For chronic ITP, the disadvantaged 10-yr survival rates persisted (for age below 20 y/o: 96.5+/-1.0% vs. 98.6+/-0.2%, p<0.0001; for age above 20 y/o: 72.7+/-1.3% vs. 86.7+/-0.4%, p<0.0001, as in Figure 2). Elder age, male gender and high CCI scores predicted worse survival in multi-variate analysis. Conclusions This study is the largest population-based epidemiology report at nationwide scale till now. Not only the results can provide a valuable demographic description for ITP in Eastern Asia, but also they confirm an inferior long-term outcome for ITP patients, which necessitates more attention to their health care. SD: standard deviation Table 1. Table 1. Figure 2. Figure 2. Figure 3. Figure 3. Disclosures Tang: Novartis: Consultancy, Honoraria.


2014 ◽  
Vol 99 (3) ◽  
pp. 286-290 ◽  
Author(s):  
Yikun Qu ◽  
Jian Xu ◽  
Chengbin Jiao ◽  
Zhuoxin Cheng ◽  
Shiyan Ren

Abstract The long-term outcomes of laparoscopic splenectomy (LS) versus open splenectomy (OS) in patients with idiopathic thrombocytopenic purpura (ITP) are not known. A retrospective analysis of 73 patients who underwent splenectomy (32 LS and 41 OS) for refractory ITP between April 2003 and June 2012 was conducted. LS was associated with shorter hospital stay (P = 0.01), less blood loss and blood transfusion during surgery, quicker resumption of oral diet (P &lt; 0.0001), and earlier drain removal (P &lt; 0.01). Conversion to OS was required in 4 patients (12.5%). Operation time was significantly longer in LS (P &lt; 0.0001). Deep venous thrombosis (DVT) was observed in 1 patient after LS and in 4 patients after OS (P = 0.52). One patient died from intraperitoneal bleeding after OS, another patient developed pulmonary embolism. Median follow-up of 36 months was performed in LS group (29 of 32, 91%) and of 46 months in OS group (35 of 41, 85%), 25 patients (86%) in LS group and 32 (91%) in OS group reached sustained complete response (P = 0.792). Kaplan-Meier analysis showed that there was no significant difference in the relapse-free survival rate between the groups (P = 0.777). In conclusion, the long-term outcome of laparoscopic splenectomy is not different from that of open splenectomy for patients with ITP.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 1077-1077
Author(s):  
Sarah Jenkinson ◽  
Amy A Kirkwood ◽  
Nicholas Goulden ◽  
Ajay J. Vora ◽  
Chris Mitchell ◽  
...  

Abstract Although outcome has improved for pediatric patients with T-ALL, ≈25% of cases relapse and prognosis post-relapse remains poor. Molecular characterisation at diagnosis can provide additional information for risk-stratification. We previously reported that patients with double NOTCH1 or NOTCH1+FBXW7 mutations (NOTCH1±FBXW7Double) have a very good outcome and should not be considered for more intensive therapy in first remission, even if slow responders or MRD-positive after induction therapy. However, recent studies have suggested that this may be modulated by the presence of coincident abnormalities such as in the PTEN gene. Truncating mutations and genomic loss of this gene have been described in T-ALL, but their prognostic impact in patients is unclear, with reports of either no effect or reduced event-free survival (EFS). Furthermore, subgroup analysis has shown that the adverse impact of a PTEN mutation is either not seen in the presence of a NOTCH1 mutation or, conversely, that it ablates the benefit of a NOTCH1 mutation. In order to determine whether these abnormalities impact on the good outcome seen in NOTCH1±FBXW7Double cases in our cohort, and whether they can refine stratification of cases with single NOTCH1 mutations (NOTCH1Single) or wild-type NOTCH1 (NOTCH1WT), we investigated PTEN genotype in samples from 145 patients treated on the MRC UKALL2003 trial and correlated this with outcome in the different subgroups. The entire coding region (exons 1-9) of the PTEN gene was screened for mutations using heteroduplex analysis. Samples with abnormal chromatograms were further investigated. Mutations were detected in 21 patients (14%); 17 (81%) had exon 7 mutations, 2 exon 6+7, and 2 exon 5 mutations. All were small insertions, deletions or indels; 89% were predicted to lead to C-terminal truncation and loss of protein function, 11% were in-frame size changes. Exon 7 mutant levels were quantified by size analysis in 19 patients; median total mutant level was 48% of all PTEN alleles (range, 10%-96%). Of note, in the 21 mutated cases, only 7 (33%) had a single mutation; 8 had 2, 3 had 3, and 3 had 4 mutations. Based on total mutant level, 11 cases were considered to have monoallelic (heterozygous) mutations and 10 cases biallelic (homozygous/hemizygous or compound heterozygous) mutations. To investigate loss of genomic material, Illumina CytoSNP-850k SNP array analysis was performed on all samples. Partial or complete loss of the PTEN gene was detected in 15 patients (10%), 12 with heterozygous and 3 homozygous loss. This data was consistent with quantitative analysis of the relative allele levels of two common intronic SNPs (rs1903858 and rs555895) studied in 76 informative patients, which indicated that in 2 of 6 informative cases with heterozygous loss, only the 3’ end of the gene was deleted. Putting together the mutation and SNP data, 32 patients (22%) had abnormalities in the PTEN gene (PTENABN), 19 (59%) scored as monoallelic (PTENMONO), and 13 (41%) biallelic (PTENBI). There was no significant difference according to overall PTEN genotype in either early response to therapy (P>.99) or MRD status at day 29 of induction therapy (P=.28). Long-term outcome also did not significantly differ, EFS at 5 years was 78% in PTENABN and 85% in PTENWT patients (P=.37), overall survival (OS) 81% and 91% respectively (P=.1). These results did not change if grouped according to PTEN type, EFS 74% in PTENMONO and 85% in PTENBI patients (P=.46), although the number of patients in these groups was very small. The incidence of PTEN abnormalities did not differ according to NOTCH1/FBXW7 genotype, 59% PTENABN patients had a NOTCH1/FBXW7 mutation compared to 67% PTENWT patients (P=.7). There was no evidence that PTEN genotype impacted on the favorable outcome of the NOTCH1±FBXW7Double group, none of the 5 PTENABNNOTCH1±FBXW7Double patients relapsed and all remain alive. Similarly, no significant difference was observed in the NOTCH1Single and NOTCH1WT patients. In conclusion, although we found that loss of PTEN through either gene mutation or genomic deletion was relatively common in pediatric T-ALL patients, including total loss of PTEN in nearly one-half of mutated patients, this appeared to have no effect on either response to treatment or long-term outcome with current therapies, and therefore screening of PTEN is not warranted in pediatric T-ALL for potential use in risk-adapted therapy. Disclosures No relevant conflicts of interest to declare.


Sign in / Sign up

Export Citation Format

Share Document