Skip to content
DraconiticResearch
Search Sources API
194,067 studies31 sourcesUpdated 50 min ago
Peer-reviewedCC BY-NC-NDZhongguo linchuang yanjiu

Construction of a risk prediction model for chemotherapy-induced taste alteration in patients with hematological malignancies

  1. 1Tianjin Medical University Cancer Institute and Hospital,National Clinical Research Center for Cancer,Tianjin ClinicalResearch Center for Cancer,Tianjin Key Laboratory of Cancer Prevention and Therapy,Tianjin 300060,China

Abstract

Objective To analyze the influencing factors of chemotherapy-induced taste alteration(CITA)in patients with hematological malignancies,and construct a risk prediction model,so as to develop a risk screening tool for this adverse reaction. Methods A total of 301 patients receiving chemotherapy in the Department of Hematology of a tertiary A hospital in Tianjin from April 2025 to December 2025 were enrolled,and their clinical data were collected.Univariate analysis and multivariate logistic regression analysis were performed to screen independent risk factors,followed by the establishment of a prediction model and nomogram plotting. Results Among the 301 enrolled patients,191 cases developed CITA with an incidence rate of 63.46%. Based on the results of multivariate logistic regression analysis,a prediction model of CITA in patients with hematological tumors was established: logit(P)=-3.839+1.852×age 29-49 years+2.006×age 50-70 years+2.443×age≥71 years+2.933×2 cycles of chemotherapy+2.767×3 cycles of chemotherapy+3.397×4 cycles of chemotherapy+2.759×5 cycles of chemotherapy+2.655×6 cycles of chemotherapy+1.467×diabetes+1.733×xerostomia or thirst+1.294× moderate oral frailty+2.605×severe oral frailty. The area under the curve(AUC)of the model was 0.906. The Hosmer-Lemeshow test(χ2=2.073,P=0.979)indicated good model calibration.After 1 000 times of Bootstrap resampling,the bias-corrected AUC was 0.884. Conclusion The established risk prediction model exhibits favorable predictive performance for CITA in patients with hematological malignancies,which can accurately identify high-risk individuals and provide an evidence for clinical prevention and targeted intervention.

Related

  1. Vaccination of patients with hematological malignancies: barriers and strategies to improve uptake
    Toni Valković, Paolo Salamon, Vanja Vasiljev +1
    Frontiers in medicinePeer-reviewedCC BYFull textGeneral medicineEurope PMC
  2. Correlates of Caregiver Burden Among Informal Caregivers of Patients With Hematological Malignancies: The Roles of Coping, Resilience, and Perceived Social Support
    Nasrin Akhter, Amin Lutful Kabir, Adnan Hasan Masud +7
    CureusPeer-reviewedCC BYFull textGeneral medicineEurope PMC
  3. Social Inequalities, Geographical Accessibility to Care, and Excess Mortality for Patients With Hematological Malignancies in France: Results From French Cancer Registries
    J. Gardy, X. Troussard, M. Maynadié +17
    Hematological OncologyPeer-reviewedLicence not statedFull textGeneral biologyOncologyHAL
  4. Prophylaxis Strategies for SARS‐CoV‐2 Infection in Adults With Hematological Malignancies in Saudi Arabia: Consensus Statements From the Working Group on COVID‐19 Management in Hematological Malignancies
    Mubarak Al‐Mansour, Ayman Alhejazi, Manal Ahmed Alsaggaf +6
    Cancer ReportsPeer-reviewedCC BY 4.0Full textInfectious diseasePMC
  5. CAR T-Cell Therapy in Hematological Malignancies: Mechanisms, Innovations, and Challenges
    Alaa A. A. Aljabali, Mohammad A. Obeid, Abdelrahim Alqudah +9
    CancersPeer-reviewedCC BY 4.0Full textOncologyCrossrefEurope PMC
BibTeX
@article{mengpei2026construction,
  title = {{Construction of a risk prediction model for chemotherapy-induced taste alteration in patients with hematological malignancies}},
  author = {ZHA Mengpei and CHEN Jing and WANG Aihong and WEI Xiaoxu and ZHOU Jing and FAN Yuanyuan},
  journal = {Zhongguo linchuang yanjiu},
  year = {2026},
  month = oct,
  doi = {10.13429/j.cnki.cjcr.2026.10.020},
  url = {https://doi.org/10.13429/j.cnki.cjcr.2026.10.020},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Construction of a risk prediction model for chemotherapy-induced taste alteration in patients with hematological malignancies
AU  - ZHA Mengpei
AU  - CHEN Jing
AU  - WANG Aihong
AU  - WEI Xiaoxu
AU  - ZHOU Jing
AU  - FAN Yuanyuan
PY  - 2026
DA  - 2026/10/26
JO  - Zhongguo linchuang yanjiu
DO  - 10.13429/j.cnki.cjcr.2026.10.020
UR  - https://doi.org/10.13429/j.cnki.cjcr.2026.10.020
AB  - Objective To analyze the influencing factors of chemotherapy-induced taste alteration(CITA)in patients with hematological malignancies,and construct a risk prediction model,so as to develop a risk screening tool for this adverse reaction. Methods A total of 301 patients receiving chemotherapy in the Department of Hematology of a tertiary A hospital in Tianjin from April 2025 to December 2025 were enrolled,and their clinical data were collected.Univariate analysis and multivariate logistic regression analysis were performed to screen independent risk factors,followed by the establishment of a prediction model and nomogram plotting. Results Among the 301 enrolled patients,191 cases developed CITA with an incidence rate of 63.46%. Based on the results of multivariate logistic regression analysis,a prediction model of CITA in patients with hematological tumors was established: logit(P)=-3.839+1.852×age 29-49 years+2.006×age 50-70 years+2.443×age≥71 years+2.933×2 cycles of chemotherapy+2.767×3 cycles of chemotherapy+3.397×4 cycles of chemotherapy+2.759×5 cycles of chemotherapy+2.655×6 cycles of chemotherapy+1.467×diabetes+1.733×xerostomia or thirst+1.294× moderate oral frailty+2.605×severe oral frailty. The area under the curve(AUC)of the model was 0.906. The Hosmer-Lemeshow test(χ2=2.073,P=0.979)indicated good model calibration.After 1 000 times of Bootstrap resampling,the bias-corrected AUC was 0.884. Conclusion The established risk prediction model exhibits favorable predictive performance for CITA in patients with hematological malignancies,which can accurately identify high-risk individuals and provide an evidence for clinical prevention and targeted intervention.
SN  - 1674-8182
ER  -