Characteristics and predictive model for diffuse large B-cell lymphoma with early chemoimmunotherapy failure
- Ying-Yu Dong 1, Qing Shi 1, Wen Wu 1, Bing-Bing Zhao 2, Di Fu 1, Peng-Peng Xu 1, Shu Cheng 1, Guilhem Bousquet 3,4,5, Wei-Li Zhao 1,5, Li Wang 1,5
- Ying-Yu Dong 1, Qing Shi 1, Wen Wu 1
- 1Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics; National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
- 2Shanghai 411 Hospital, Shanghai, China.
- 3Université Sorbonne Paris Nord, Villetaneuse, France.
- 4Assistance Publique Hôpitaux de Paris, Hôpital Avicenne, Service d'Oncologie Médicale, Bobigny, France.
- 5Pôle de Recherches Sino-Français en Science du Vivant et Génomique, Laboratory of Molecular Pathology, Shanghai, China.
- 0Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics; National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Identifying early chemoimmunotherapy failure (ECF) in diffuse large B-cell lymphoma is crucial. This study developed a predictive model for ECF, identifying key clinical and molecular factors to improve patient outcomes.
Area Of Science
- Hematology
- Oncology
- Genetics
Background
- Refractory or relapsed diffuse large B-cell lymphoma (DLBCL) has poor outcomes.
- Early chemoimmunotherapy failure (ECF) within 12 months of diagnosis has a dismal 2-year overall survival (OS) of 24.7%.
Purpose Of The Study
- To identify predictors of ECF in DLBCL patients.
- To develop a predictive model for early recognition of ECF.
- To improve therapeutic strategies and outcomes for chemo-resistant DLBCL patients.
Main Methods
- Retrospective analysis of 2038 newly diagnosed DLBCL patients treated with R-CHOP/RminiCHOP or R-CHOP-based immunochemotherapy.
- Multivariate analysis to identify independent predictors of ECF.
- Development and validation of a nomogram-based ECF prediction model.
Main Results
- ECF patients were associated with elderly age, advanced Ann Arbor stage, elevated LDH, poor performance status, extranodal involvement, double expressor lymphoma (DEL), and non-GCB subtype.
- TP53, FOXO1, and FBXW7 mutations were frequent in ECF.
- Elderly age, advanced stage, elevated LDH, DEL, and TP53 or FOXO1 mutations were independent predictors of ECF.
Conclusions
- A nomogram predicting ECF was established with good predictive power in both Chinese and Western cohorts.
- The ECF prediction model enables early identification of high-risk patients.
- Optimizing therapeutic strategies for early identified ECF patients can improve outcomes.
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