Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib

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Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib. / Cortes, Jorge E; Khoury, Hanna J; Kantarjian, Hagop M; Lipton, Jeff H; Kim, Dong-Wook; Schafhausen, Philippe; Matczak, Ewa; Leip, Eric; Noonan, Kay; Brümmendorf, Tim H; Gambacorti-Passerini, Carlo.

In: AM J HEMATOL, Vol. 91, No. 12, 12.2016, p. 1206-1214.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Cortes, JE, Khoury, HJ, Kantarjian, HM, Lipton, JH, Kim, D-W, Schafhausen, P, Matczak, E, Leip, E, Noonan, K, Brümmendorf, TH & Gambacorti-Passerini, C 2016, 'Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib', AM J HEMATOL, vol. 91, no. 12, pp. 1206-1214. https://doi.org/10.1002/ajh.24536

APA

Cortes, J. E., Khoury, H. J., Kantarjian, H. M., Lipton, J. H., Kim, D-W., Schafhausen, P., Matczak, E., Leip, E., Noonan, K., Brümmendorf, T. H., & Gambacorti-Passerini, C. (2016). Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib. AM J HEMATOL, 91(12), 1206-1214. https://doi.org/10.1002/ajh.24536

Vancouver

Bibtex

@article{72ca74eb69164389952cd34e86b9efd4,
title = "Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib",
abstract = "Bosutinib is an Src/Abl tyrosine kinase inhibitor (TKI) indicated for adults with Ph+ chronic myeloid leukemia (CML) resistant/intolerant to prior TKIs. This long-term update of an ongoing phase 1/2 study evaluated the efficacy and safety of third-/fourth-line bosutinib in adults with chronic phase (CP) CML. Median durations of treatment and follow-up were 8.6 (range, 0.2-87.7) months and 32.7 (0.3-93.3) months, respectively. Cumulative confirmed complete hematologic response (cCHR) and major cytogenetic response (MCyR) rates were 74% (95% CI, 65-81%) and 40% (31-50%), respectively; Kaplan-Meier (K-M) probability of maintaining cCHR or MCyR at 4 years was 63% (95% CI, 50-73%) and 69% (52-81%). Cumulative incidence of on-treatment disease progression (PD)/death at 4 years was 24% (95% CI, 17-33%); K-M 4-year overall survival was 78% (68-85%). Baseline Ph+ cells ≤35 vs. ≥95% was prognostic of MCyR and CCyR by 3 and 6 months, increased baseline basophils was prognostic of PD/death, and no prior response to second-line TKI was prognostic of death. Common adverse events included diarrhea (83%), nausea (48%), vomiting (38%), and thrombocytopenia (39%). Bosutinib demonstrates durable efficacy and a toxicity profile similar to previous bosutinib studies in CP CML patients resistant/intolerant to multiple TKIs, representing an important treatment option for patients in this setting. This trial is registered at www.clinicaltrials.gov (NCT00261846). Am. J. Hematol. 91:1206-1214, 2016. {\textcopyright} 2016 Wiley Periodicals, Inc.",
author = "Cortes, {Jorge E} and Khoury, {Hanna J} and Kantarjian, {Hagop M} and Lipton, {Jeff H} and Dong-Wook Kim and Philippe Schafhausen and Ewa Matczak and Eric Leip and Kay Noonan and Br{\"u}mmendorf, {Tim H} and Carlo Gambacorti-Passerini",
note = "{\textcopyright} 2016 Wiley Periodicals, Inc.",
year = "2016",
month = dec,
doi = "10.1002/ajh.24536",
language = "English",
volume = "91",
pages = "1206--1214",
journal = "AM J HEMATOL",
issn = "0361-8609",
publisher = "Wiley-Liss Inc.",
number = "12",

}

RIS

TY - JOUR

T1 - Long-term bosutinib for chronic phase chronic myeloid leukemia after failure of imatinib plus dasatinib and/or nilotinib

AU - Cortes, Jorge E

AU - Khoury, Hanna J

AU - Kantarjian, Hagop M

AU - Lipton, Jeff H

AU - Kim, Dong-Wook

AU - Schafhausen, Philippe

AU - Matczak, Ewa

AU - Leip, Eric

AU - Noonan, Kay

AU - Brümmendorf, Tim H

AU - Gambacorti-Passerini, Carlo

N1 - © 2016 Wiley Periodicals, Inc.

PY - 2016/12

Y1 - 2016/12

N2 - Bosutinib is an Src/Abl tyrosine kinase inhibitor (TKI) indicated for adults with Ph+ chronic myeloid leukemia (CML) resistant/intolerant to prior TKIs. This long-term update of an ongoing phase 1/2 study evaluated the efficacy and safety of third-/fourth-line bosutinib in adults with chronic phase (CP) CML. Median durations of treatment and follow-up were 8.6 (range, 0.2-87.7) months and 32.7 (0.3-93.3) months, respectively. Cumulative confirmed complete hematologic response (cCHR) and major cytogenetic response (MCyR) rates were 74% (95% CI, 65-81%) and 40% (31-50%), respectively; Kaplan-Meier (K-M) probability of maintaining cCHR or MCyR at 4 years was 63% (95% CI, 50-73%) and 69% (52-81%). Cumulative incidence of on-treatment disease progression (PD)/death at 4 years was 24% (95% CI, 17-33%); K-M 4-year overall survival was 78% (68-85%). Baseline Ph+ cells ≤35 vs. ≥95% was prognostic of MCyR and CCyR by 3 and 6 months, increased baseline basophils was prognostic of PD/death, and no prior response to second-line TKI was prognostic of death. Common adverse events included diarrhea (83%), nausea (48%), vomiting (38%), and thrombocytopenia (39%). Bosutinib demonstrates durable efficacy and a toxicity profile similar to previous bosutinib studies in CP CML patients resistant/intolerant to multiple TKIs, representing an important treatment option for patients in this setting. This trial is registered at www.clinicaltrials.gov (NCT00261846). Am. J. Hematol. 91:1206-1214, 2016. © 2016 Wiley Periodicals, Inc.

AB - Bosutinib is an Src/Abl tyrosine kinase inhibitor (TKI) indicated for adults with Ph+ chronic myeloid leukemia (CML) resistant/intolerant to prior TKIs. This long-term update of an ongoing phase 1/2 study evaluated the efficacy and safety of third-/fourth-line bosutinib in adults with chronic phase (CP) CML. Median durations of treatment and follow-up were 8.6 (range, 0.2-87.7) months and 32.7 (0.3-93.3) months, respectively. Cumulative confirmed complete hematologic response (cCHR) and major cytogenetic response (MCyR) rates were 74% (95% CI, 65-81%) and 40% (31-50%), respectively; Kaplan-Meier (K-M) probability of maintaining cCHR or MCyR at 4 years was 63% (95% CI, 50-73%) and 69% (52-81%). Cumulative incidence of on-treatment disease progression (PD)/death at 4 years was 24% (95% CI, 17-33%); K-M 4-year overall survival was 78% (68-85%). Baseline Ph+ cells ≤35 vs. ≥95% was prognostic of MCyR and CCyR by 3 and 6 months, increased baseline basophils was prognostic of PD/death, and no prior response to second-line TKI was prognostic of death. Common adverse events included diarrhea (83%), nausea (48%), vomiting (38%), and thrombocytopenia (39%). Bosutinib demonstrates durable efficacy and a toxicity profile similar to previous bosutinib studies in CP CML patients resistant/intolerant to multiple TKIs, representing an important treatment option for patients in this setting. This trial is registered at www.clinicaltrials.gov (NCT00261846). Am. J. Hematol. 91:1206-1214, 2016. © 2016 Wiley Periodicals, Inc.

U2 - 10.1002/ajh.24536

DO - 10.1002/ajh.24536

M3 - SCORING: Journal article

C2 - 27531525

VL - 91

SP - 1206

EP - 1214

JO - AM J HEMATOL

JF - AM J HEMATOL

SN - 0361-8609

IS - 12

ER -