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Clinical use and adverse effects of tyrosine kinase inhibitors in patients with chronic myeloid leukemia: The role of comorbidities.

2/5 보강
Leukemia research 2026 Vol.166() p. 108235 Chronic Myeloid Leukemia Treatments
Retraction 확인
출처
PubMed DOI OpenAlex 마지막 보강 2026-04-30

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
102 patients with chronic-phase CML who were diagnosed between 1997 and 2023 and followed at a single outpatient clinic.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] Comorbidities, particularly hypothyroidism and cardiovascular diseases, significantly influence the development of TKI-related adverse effects in patients with CML. Careful assessment of comorbidities and concomitant medications is essential for optimal TKI selection and toxicity management in clinical practice.
OpenAlex 토픽 · Chronic Myeloid Leukemia Treatments Acute Myeloid Leukemia Research HER2/EGFR in Cancer Research

Kır S, Abdullayeva N, Yılmazer A, Saydam G, Hekimgil M, Demirci Z, Soyer N

📝 환자 설명용 한 줄

[OBJECTIVE] Chronic myeloid leukemia (CML) is frequently accompanied by comorbidities that may influence the tolerability of tyrosine kinase inhibitors (TKIs).

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p = 0.037
  • p-value p = 0.031

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↓ .bib ↓ .ris
APA Selin Kır, Nigar Abdullayeva, et al. (2026). Clinical use and adverse effects of tyrosine kinase inhibitors in patients with chronic myeloid leukemia: The role of comorbidities.. Leukemia research, 166, 108235. https://doi.org/10.1016/j.leukres.2026.108235
MLA Selin Kır, et al.. "Clinical use and adverse effects of tyrosine kinase inhibitors in patients with chronic myeloid leukemia: The role of comorbidities.." Leukemia research, vol. 166, 2026, pp. 108235.
PMID 41996824

Abstract

[OBJECTIVE] Chronic myeloid leukemia (CML) is frequently accompanied by comorbidities that may influence the tolerability of tyrosine kinase inhibitors (TKIs). This study aimed to evaluate TKI-related adverse effects and their association with comorbidities in patients with CML.

[MATERIALS AND METHODS] This retrospective study analyzed clinical data from 102 patients with chronic-phase CML who were diagnosed between 1997 and 2023 and followed at a single outpatient clinic.

[RESULTS] Among the 102 patients, the most common comorbidities were hypertension, diabetes mellitus, coronary artery disease, hypothyroidism, hyperlipidemia, chronic kidney disease, and chronic obstructive pulmonary disease. Hypothyroidism was significantly associated with the development of adverse effects in patients receiving first-line imatinib therapy (p = 0.037). In system-based analyses, adverse effects were more frequently observed in imatinib-treated patients with oncological comorbidities compared with those without (p = 0.031). Additionally, adverse effects were significantly less frequent in patients treated with imatinib than in those receiving other TKIs (p = 0.048). When all TKIs were evaluated together, cardiovascular comorbidities were the only system significantly associated with an increased risk of adverse effects (p = 0.015).

[CONCLUSION] Comorbidities, particularly hypothyroidism and cardiovascular diseases, significantly influence the development of TKI-related adverse effects in patients with CML. Careful assessment of comorbidities and concomitant medications is essential for optimal TKI selection and toxicity management in clinical practice.