2014
DOI: 10.1371/journal.pone.0085554
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Survival of Adults with Acute Lymphoblastic Leukemia in Germany and the United States

Abstract: BackgroundAdulthood acute lymphoblastic leukemia (ALL) is a rare disease. In contrast to childhood ALL, survival for adults with ALL is poor. Recently, new protocols, including use of pediatric protocols in young adults, have improved survival in clinical trials. Here, we examine population level survival in Germany and the United States (US) to gain insight into the extent to which changes in clinical trials have translated into better survival on the population level.MethodsData were extracted from the Surve… Show more

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Cited by 89 publications
(69 citation statements)
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“…1 Improved survival primarily stems from decreased incidence of relapse, with very little improvement for more than 20 years in survival rates for children who relapse. [2][3][4] In contrast, overall survival for adults with ALL is quite poor (30% to 40%), 5,6 and relapsed ALL remains particularly challenging for all age groups, making it a leading cause of cancer deaths in children and carrying a dismal prognosis in adults. 2,4,7 Most children in first relapse will achieve a second complete remission (CR2), in contrast to the adult population, in which CR2 rates are 50% at best.…”
Section: Introductionmentioning
confidence: 99%
“…1 Improved survival primarily stems from decreased incidence of relapse, with very little improvement for more than 20 years in survival rates for children who relapse. [2][3][4] In contrast, overall survival for adults with ALL is quite poor (30% to 40%), 5,6 and relapsed ALL remains particularly challenging for all age groups, making it a leading cause of cancer deaths in children and carrying a dismal prognosis in adults. 2,4,7 Most children in first relapse will achieve a second complete remission (CR2), in contrast to the adult population, in which CR2 rates are 50% at best.…”
Section: Introductionmentioning
confidence: 99%
“…However, relapse eventually occurs, and the 5 year overall survival (OS) is 42–63% for adolescents and young adults, 24.1% for patients between the ages of 40–59, and 17.7% for patients between the ages of 60–69 (5). Historically, age, a high leukocyte count at presentation, poor response to treatment, T-cell immunophenotype, cytogenetic profile of the disease and extranodal presentation of the disease have been considered adverse clinical prognostic factors in adult ALL.…”
Section: Discussionmentioning
confidence: 99%
“…Adults have the poorest 5-year OS rate: 24.1% for patients between the ages of 40 and 59 and an even lower rate of 17.7% for patients between the ages of 60 and 69. 21 Although the exact OS percentage can vary based on how the age range is defined for pediatric, AYA, and adult patients, the trend is nonetheless clear that OS decreases substantially with increased age. The exception is infants younger than age 1, which is an age group that has not seen any improvement in survival over the past 30 years.…”
Section: All-e All-fmentioning
confidence: 99%