Treatment of Frail Older Adults and Elderly Patients With Philadelphia Chromosome-negative Acute Lymphoblastic Leukemia: Results of a Prospective Trial With Minimal Chemotherapy

2020 ◽  
Vol 20 (8) ◽  
pp. e513-e522
Author(s):  
Josep-Maria Ribera ◽  
Olga García ◽  
Eduardo Cerello Chapchap ◽  
Cristina Gil ◽  
José González-Campos ◽  
...  
Cancer ◽  
2007 ◽  
Vol 109 (10) ◽  
pp. 2068-2076 ◽  
Author(s):  
Oliver G. Ottmann ◽  
Barbara Wassmann ◽  
Heike Pfeifer ◽  
Aristoteles Giagounidis ◽  
Matthias Stelljes ◽  
...  

Blood ◽  
2009 ◽  
Vol 113 (19) ◽  
pp. 4489-4496 ◽  
Author(s):  
Adele K. Fielding ◽  
Jacob M. Rowe ◽  
Susan M. Richards ◽  
Georgina Buck ◽  
Anthony V. Moorman ◽  
...  

Abstract Prospective data on the value of allogeneic hematopoietic stem cell transplantation (alloHSCT) in Philadelphia chromosome–positive (Ph+) acute lymphoblastic leukemia (ALL) are limited. The UKALLXII/ECOG 2993 study evaluated the outcome of assigning alloHSCT with a sibling (sib) or matched unrelated donor (MUD) to patients younger than 55 years of age achieving complete remission (CR). The CR rate of 267 patients, median age 40, was 82%. Twenty-eight percent of patients proceeded to alloHSCT in first CR. Age older than 55 years or a pre-HSCT event were the most common reasons for failure to progress to alloHSCT. At 5 years, overall survival (OS) was 44% after sib alloHSCT, 36% after MUD alloHSCT, and 19% after chemotherapy. After adjustment for sex, age, and white blood count and excluding chemotherapy-treated patients who relapsed or died before the median time to alloHSCT, only relapse-free survival remained significantly superior in the alloHSCT group (odds ratio 0.31, 95% confidence interval 0.16-0.61). An intention-to-treat analysis, using the availability or not of a matched sibling donor, showed 5-year OS to be nonsignificantly better at 34% with a donor versus 25% with no donor. This prospective trial in adult Ph+ ALL indicates a modest but significant benefit to alloHSCT. This trial has been registered with clinicaltrials.gov under identifier NCT00002514 and as ISRCTN77346223.


2006 ◽  
Vol 0 (0) ◽  
pp. 061114074547002-??? ◽  
Author(s):  
Juan-Manuel Sancho ◽  
Josep-Maria Ribera ◽  
Blanca Xicoy ◽  
Mireia Morgades ◽  
Albert Oriol ◽  
...  

2021 ◽  
pp. 24-28
Author(s):  
Kazuki Tanimura ◽  
Kai Yamasaki ◽  
Yuki Okuhiro ◽  
Kota Hira ◽  
Chika Nitani ◽  
...  

Ponatinib is a third-generation tyrosine kinase inhibitor (TKI) reported to show a higher efficacy for adult Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) than other TKIs. However, few studies describe ponatinib for pediatric Ph+ALL; therefore, the efficacy, safety, and optimal dosage have not been determined. Here, we report a 3-year-old girl with Ph+ALL treated by a ponatinib-containing regimen with therapeutic drug monitoring in the plasma and cerebrospinal fluid (CSF). In our case, a ponatinib-containing regimen was able to keep minimal residual disease negative, and the pharmacokinetics (PKs) of plasma ponatinib resembled that previously reported in adults. Penetration to the CSF was extremely limited. Thus, ponatinib was feasible and effective for a child with Ph+ALL, although the plasma concentration of ponatinib varied significantly throughout the treatment. The appropriate dosage should be confirmed in a prospective trial, including a detailed PK study.


2020 ◽  
Vol 13 (6) ◽  
pp. 124 ◽  
Author(s):  
Sandrine Niyongere ◽  
Gabriela Sanchez-Petitto ◽  
Jack Masur ◽  
Maria R. Baer ◽  
Vu H. Duong ◽  
...  

Outcomes of acute lymphoblastic leukemia (ALL) in older adults treated with chemotherapy are poor. The CD19/CD3 bispecific T-cell engager (BiTE) antibody blinatumomab is approved for refractory, relapsed or minimal/measurable residual disease (MRD)-positive B-cell ALL, but there is little experience in the upfront setting, including in older patients. We retrospectively analyzed outcomes of blinatumomab monotherapy in five newly diagnosed Philadelphia chromosome-negative B-cell ALL patients over 70 years. Three had cytokine release syndrome, treated with dexamethasone and/or tocilizumab, and four patients had neurotoxicity, treated with dexamethasone, without blinatumomab interruption. All five achieved complete remission (CR) after cycle one, three with undetectable MRD. All five were alive at 8 to 15 months. Three remained in MRD-negative CR. Two relapsed after cycle 3, one with extramedullary disease. In our small cohort of patients over 70 years, blinatumomab was safe initial therapy and produced a high response rate.


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