dc.contributor.author | Korkmaz, Serdal | |
dc.contributor.author | Eser, Bulent | |
dc.contributor.author | Altuntas, Fevzi | |
dc.contributor.author | Tiryaki, Tarik Onur | |
dc.contributor.author | Ulas, Turgay | |
dc.contributor.author | ÖZATLI, DÜZGÜN | |
dc.contributor.author | Akpinar, Seval | |
dc.contributor.author | Dogu, Mehmet Hilmi | |
dc.contributor.author | ÇELİK, SERHAT | |
dc.contributor.author | Ekinci, Omer | |
dc.contributor.author | Hindilerden, Ipek Yonal | |
dc.contributor.author | Dal, Mehmet Sinan | |
dc.contributor.author | Davulcu, Eren Arslan | |
dc.contributor.author | Tekinalp, Atakan | |
dc.contributor.author | Hindilerden, Fehmi | |
dc.contributor.author | Ozcan, Busra Gokce | |
dc.contributor.author | HACIBEKİROĞLU, TUBA | |
dc.contributor.author | ERKURT, MEHMET ALİ | |
dc.contributor.author | Bagci, Metin | |
dc.contributor.author | Namdaroglu, Sinem | |
dc.contributor.author | Korkmaz, Gulten | |
dc.contributor.author | Bilgir, Oktay | |
dc.contributor.author | ÇAĞLIYAN, GÜLSÜM AKGÜN | |
dc.contributor.author | Ozturk, Hacer Berna Afacan | |
dc.contributor.author | Serin, Istemi | |
dc.contributor.author | TURGUT, BURHAN | |
dc.date.accessioned | 2022-07-04T16:28:53Z | |
dc.date.available | 2022-07-04T16:28:53Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Akpinar S., Dogu M. H. , ÇELİK S., Ekinci O., Hindilerden I. Y. , Dal M. S. , Davulcu E. A. , Tekinalp A., Hindilerden F., Ozcan B. G. , et al., "The Real-World Experience With Single Agent Ibrutinib in Relapsed/Refractory CLL", CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, cilt.22, sa.3, ss.169-173, 2022 | |
dc.identifier.issn | 2152-2650 | |
dc.identifier.other | av_e76d5d2b-0c13-4e76-960a-d4f1c2ceb72d | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/185157 | |
dc.identifier.uri | https://doi.org/10.1016/j.clml.2021.09.010 | |
dc.description.abstract | We evaluated the safety and efficacy of single-agent ibrutinib in 200 patients presenting with relapsed/refractory CLL in real-world settings. With an estimated median OS of 52 months, 146 patients (75%) achieved at least PR; 16 (8.7%) patients discontinued ibrutinib due to adverse events. The results indicate good safety and efficacy for single-agent ibrutinib in R/R CLL in daily practice. | |
dc.language.iso | eng | |
dc.subject | Health Sciences | |
dc.subject | Onkoloji | |
dc.subject | Oncology | |
dc.subject | Hematology | |
dc.subject | Tıp | |
dc.subject | HEMATOLOJİ | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Hematoloji | |
dc.subject | İç Hastalıkları | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Klinik Tıp | |
dc.subject | ONKOLOJİ | |
dc.subject | Sağlık Bilimleri | |
dc.title | The Real-World Experience With Single Agent Ibrutinib in Relapsed/Refractory CLL | |
dc.type | Makale | |
dc.relation.journal | CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | |
dc.contributor.department | Ondokuz Mayıs Üniversitesi , , | |
dc.identifier.volume | 22 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 169 | |
dc.identifier.endpage | 173 | |
dc.contributor.firstauthorID | 3398178 | |