Scopus Eşleşmesi Bulundu
2
Atıf
36
Cilt
169-177
Sayfa
🔓
Açık Erişim
Scopus Yazarları: Leylagul Kaynar, Bahriye Payzın, Mehmet Hilmi Doğu, Yahya Büyükaşık, Fatih Demirkan, Rafiye Çiftçiler, Ömür Gökmen Sevindik, Ali İrfan Emre Tekgündüz, Mehmet Ali Erkurt, Filiz Vural, Burhan Turgut, Volkan Karakuş, Fevzi Altuntaş
Özet
Objective: Significant developments occurred in the clinical management of acute lymphoblastic leukemia (ALL) in adults in recent decades. However, treatment results are still not satisfactory, especially in routine practice. The objective of this study was to evaluate the general clinical features, treatment details, and outcomes of a large group of patients followed in multiple centers in Turkey with a diagnosis of ALL. Materials and Methods: A retrospective analysis of the data of patients with ALL was made, the patients having been diagnosed and treated between January 2003 and June 2017 by different protocols in the hematology clinics of ten different centers. A total of 288 patients, aged between 17 and 76 years old, were included in the study. In this retrospective multicenter analysis of patients with ALL, classification of patients was performed based on treatment period, Philadelphia chromosome positivity, treatment regimen, and administration of allogeneic hematopoietic stem cell transplantation (allo-HSCT). Results: The majority of cases were B-cell in origin, while 224 patients had B-ALL and 64 of the patients had T-ALL. Median follow-up duration for all patients was 18.2 months (range: 0.03-161 months). Philadelphia chromosome positivity was determined in 49 patients (21.9%), and 54 patients (18.8%) were receiving allo-HSCT. After induction chemotherapy, 219 patients (76.0%) achieved complete remission, 32 patients (11.2%) were evaluated as treatment refractory, and 37 patients (12.8%) were deceased. Median overall survival was 47.7 months (95% confidence interval: 36.1-59.2) and median disease-free survival was 23.4 months (95% confidence interval: 6.7-40.0) for all patients. Conclusion: Multicenter studies are extremely important for defining the specific clinical features of a particular disease. The results of this study will make a significant contribution to the literature as they reflect real-life data providing valuable information about the Turkish ALL patient profile.
Anahtar Kelimeler (Scopus)
Acute lymphoblastic leukemia
Pediatric regimen
Pediatric-inspired regimen
Philadelphia chromosome
Scimago Dergi Bilgisi
Otomatik ISSN Eşleştirmesi
2019 yılı verileri
Turkish Journal of Haematology
Q3
SJR Quartile
0,312
SJR Skoru
25
H-Index
🔓
Açık Erişim
Kategoriler: Hematology (Q3)
Alanlar: Medicine
Ülke: Turkey
· AVES
Bu bilgiler makale yılına göre Scimago veritabanından ISSN eşleştirmesiyle otomatik getirilmektedir.
Dergi sıralama verileri Scimago'nun ilgili yılı baz alınmaktadır.
Anahtar Kelimeler
Acute lymphoblastic leukemia
Pediatric regimen
Pediatric-inspired regimen
Philadelphia chromosome
Makale Bilgileri
Dergi
Turkish Journal of Hematology
ISSN
1300-7777
Yıl
2019
/ 5. ay
Cilt / Sayı
36
/ 3
Sayfalar
169 – 177
Makale Türü
Özgün Makale
Hakemlik
Hakemli
Endeks
SCI-Expanded
Yayın Dili
İngilizce
Kapsam
Uluslararası
Toplam Yazar
13 kişi
Erişim Türü
Basılı+Elektronik
Erişim Linki
Makaleye Git
Alan
Sağlık Bilimleri Temel Alanı-
Hematoloji
YÖKSİS Yazar Kaydı
Yazar Adı
ÇİFTÇİLER RAFİYE,SEVİNDİK ÖMÜR GÖKMEN,TEKGÜNDÜZ ALİ İRFAN EMRE,ERKURT MEHMET ALİ,VURAL FİLİZ,TURGUT BURHAN,KAYNAR LEYLAGÜL,PAYZIN KADRİYE BAHRİYE,DOĞU MEHMET HİLMİ,KARAKUŞ VOLKAN,ALTUNTAŞ FEVZİ,BÜYÜKAŞIK YAHYA,DEMİRKAN FATİH
YÖKSİS ID
4544231
Hızlı Erişim
Metrikler
Scopus Atıf
2
Yazar Sayısı
13