001     130805
005     20240228145554.0
024 7 _ |a 10.1038/leu.2017.92
|2 doi
024 7 _ |a pmid:28322237
|2 pmid
024 7 _ |a 0887-6924
|2 ISSN
024 7 _ |a 1476-5551
|2 ISSN
024 7 _ |a altmetric:20917080
|2 altmetric
037 _ _ |a DKFZ-2017-05883
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |a Kayser, Sabine
|0 P:(DE-He78)ce3cd0df5fbbdf8768f6f1cd543bce72
|b 0
|e First author
|u dkfz
245 _ _ |a Characteristics and outcome of patients with therapy-related acute promyelocytic leukemia front-line treated with or without arsenic trioxide.
260 _ _ |a Basingstoke
|c 2017
|b Nature Publ. Group
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1525863094_13985
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Therapy-related acute promyelocytic leukemia (t-APL) is relatively rare, with limited data on outcome after treatment with arsenic trioxide (ATO) compared to standard intensive chemotherapy (CTX). We evaluated 103 adult t-APL patients undergoing treatment with all-trans retinoic acid (ATRA) alone (n=7) or in combination with ATO (n=24), CTX (n=53), or both (n=19). Complete remissions were achieved after induction therapy in 57% with ATRA, 100% with ATO/ATRA, 78% with CTX/ATRA, and 95% with CTX/ATO/ATRA. Early death rates were 43% for ATRA, 0% for ATO/ATRA, 12% for CTX/ATRA and 5% for CTX/ATO/ATRA. Three patients relapsed, two developed therapy-related acute myeloid leukemia and 13 died in remission including seven patients with recurrence of the prior malignancy. Median follow-up for survival was 3.7 years. None of the patients treated with ATRA alone survived beyond one year. Event-free survival was significantly higher after ATO-based therapy (95%, 95% CI, 82-99%) as compared to CTX/ATRA (78%, 95% CI, 64-87%; P=0.042), if deaths due to recurrence of the prior malignancy were censored. The estimated 2-year overall survival in intensively treated patients was 88% (95% CI, 80-93%) without difference according to treatment (P=0.47). ATO when added to ATRA or CTX/ATRA is feasible and leads to better outcomes as compared to CTX/ATRA in t-APL.
536 _ _ |a 317 - Translational cancer research (POF3-317)
|0 G:(DE-HGF)POF3-317
|c POF3-317
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
700 1 _ |a Krzykalla, J.
|0 P:(DE-He78)5a7a75d1b29b770f98f1bb2062fc3df9
|b 1
|u dkfz
700 1 _ |a Elliott, M. A.
|b 2
700 1 _ |a Norsworthy, K.
|b 3
700 1 _ |a Gonzales, P.
|b 4
700 1 _ |a Hills, R. K.
|b 5
700 1 _ |a Baer, M. R.
|b 6
700 1 _ |a Ráčil, Z.
|b 7
700 1 _ |a Mayer, J.
|b 8
700 1 _ |a Novak, J.
|b 9
700 1 _ |a Žák, P.
|b 10
700 1 _ |a Szotkowski, T.
|b 11
700 1 _ |a Grimwade, D.
|b 12
700 1 _ |a Russell, N. H.
|b 13
700 1 _ |a Walter, R. B.
|b 14
700 1 _ |a Estey, E. H.
|b 15
700 1 _ |a Westermann, J.
|b 16
700 1 _ |a Görner, M.
|b 17
700 1 _ |a Benner, A.
|0 P:(DE-He78)e15dfa1260625c69d6690a197392a994
|b 18
|u dkfz
700 1 _ |a Krämer, A.
|0 P:(DE-He78)493c5fbf69f1b20df6f048712f3ad4a0
|b 19
|u dkfz
700 1 _ |a Smith, B. D.
|b 20
700 1 _ |a Burnett, A. K.
|b 21
700 1 _ |a Thiede, C.
|b 22
700 1 _ |a Röllig, C.
|b 23
700 1 _ |a Ho, A. D.
|b 24
700 1 _ |a Ehninger, G.
|b 25
700 1 _ |a Schlenk, Richard
|0 P:(DE-He78)d8a0e60e5e095f3161ee0de3712409bc
|b 26
|u dkfz
700 1 _ |a Tallman, M. S.
|b 27
700 1 _ |a Levis, M. J.
|b 28
700 1 _ |a Platzbecker, U.
|b 29
773 _ _ |a 10.1038/leu.2017.92
|g Vol. 31, no. 11, p. 2347 - 2354
|0 PERI:(DE-600)2008023-2
|n 11
|p 2347 - 2354
|t Leukemia
|v 31
|y 2017
|x 1476-5551
909 C O |o oai:inrepo02.dkfz.de:130805
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 0
|6 P:(DE-He78)ce3cd0df5fbbdf8768f6f1cd543bce72
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 1
|6 P:(DE-He78)5a7a75d1b29b770f98f1bb2062fc3df9
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 18
|6 P:(DE-He78)e15dfa1260625c69d6690a197392a994
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 19
|6 P:(DE-He78)493c5fbf69f1b20df6f048712f3ad4a0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 26
|6 P:(DE-He78)d8a0e60e5e095f3161ee0de3712409bc
913 1 _ |a DE-HGF
|l Krebsforschung
|1 G:(DE-HGF)POF3-310
|0 G:(DE-HGF)POF3-317
|2 G:(DE-HGF)POF3-300
|v Translational cancer research
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF3
|b Gesundheit
914 1 _ |y 2017
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0310
|2 StatID
|b NCBI Molecular Biology Database
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b LEUKEMIA : 2015
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Thomson Reuters Master Journal List
915 _ _ |a WoS
|0 StatID:(DE-HGF)0110
|2 StatID
|b Science Citation Index
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
915 _ _ |a WoS
|0 StatID:(DE-HGF)0111
|2 StatID
|b Science Citation Index Expanded
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
915 _ _ |a IF >= 10
|0 StatID:(DE-HGF)9910
|2 StatID
|b LEUKEMIA : 2015
920 1 _ |0 I:(DE-He78)G330-20160331
|k G330
|l KKE Molekulare Hämatologie/Onkologie
|x 0
920 1 _ |0 I:(DE-He78)C060-20160331
|k C060
|l Biostatistik
|x 1
920 1 _ |0 I:(DE-He78)G040-20160331
|k G040
|l Klinische Studienzentrale
|x 2
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)G330-20160331
980 _ _ |a I:(DE-He78)C060-20160331
980 _ _ |a I:(DE-He78)G040-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21