Pentostatin, Cyclophosphamide, and Rituximab Followed by Alemtuzumab for Relapsed or Refractory Chronic Lymphocytic Leukemia: A Phase 2 Trial of the ECOG-Acrin Cancer Research Group (E2903).
Aged
Alemtuzumab
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Cyclophosphamide
/ administration & dosage
Disease-Free Survival
Female
Humans
Leukemia, Lymphocytic, Chronic, B-Cell
/ drug therapy
Male
Middle Aged
Pentostatin
/ administration & dosage
Rituximab
/ administration & dosage
Survival Rate
Alemtuzumab
Chemoimmunotherapy
Chronic lymphocytic leukemia
Cyclophosphamide
Pentostatin
Refractory disease
Relapse
Rituximab
Journal
Acta haematologica
ISSN: 1421-9662
Titre abrégé: Acta Haematol
Pays: Switzerland
ID NLM: 0141053
Informations de publication
Date de publication:
2019
2019
Historique:
received:
10
03
2019
accepted:
13
03
2019
pubmed:
25
7
2019
medline:
18
3
2020
entrez:
24
7
2019
Statut:
ppublish
Résumé
Patients with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) may benefit from salvage chemoimmunotherapy (CIT). To explore further the use of CIT in the pre-novel agent era, ECOG-ACRIN undertook a phase 2 trial (E2903) for R/R CLL utilizing pentostatin, cyclophosphamide, and rituximab (PCR) followed by a consolidation course of alemtuzumab. This trial enrolled 102 patients with a median age of 64 years. Treatment consisted of 6 cycles of PCR followed by alemtuzumab for either 4 or 18 weeks depending on the initial response to PCR. The overall response after PCR (complete remission, CR, nodular partial remission, nPR, and partial remission, PR) was 55%. Major responses (CR or nPR) were achieved in 6%. The median overall survival (OS) and the median progression-free survival were 28 and 12 months, respectively. The most serious nonlethal adverse events were myelosuppression, febrile neutropenia, fatigue, nausea, and hyponatremia. PCR is an effective and well-tolerated nucleoside-based regimen for heavily pretreated CLL patients with R/R disease. The addition of alemtuzumab to CLL patients with a minor response (PR) or stable disease did not result in a significant number of higher responses (CR or nPR) nor an improvement in OS.
Identifiants
pubmed: 31336367
pii: 000500164
doi: 10.1159/000500164
pmc: PMC6834875
mid: NIHMS1031250
doi:
Substances chimiques
Pentostatin
395575MZO7
Alemtuzumab
3A189DH42V
Rituximab
4F4X42SYQ6
Cyclophosphamide
8N3DW7272P
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
224-232Subventions
Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189971
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233320
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189825
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233234
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189859
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233277
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA232760
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180790
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180794
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180799
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180853
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189956
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA196172
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180791
Pays : United States
Informations de copyright
© 2019 S. Karger AG, Basel.
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