Ou Bai
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Ou Bai has a total of 319 co-authors. Here are the top co-authors by number of shared publications:
Wei Guo
Department of Hematology, The First Hospital of Jilin University
34 shared publicationsYangzhi Zhao
Department of Hematology, The First Hospital of Jilin University
16 shared publicationsHaotian Wang
Department of Hematology, The First Hospital of Jilin University
14 shared publications- Wei Guo
Department of Hematology the First Hospital of Jilin University Changchun China
14 shared publications Jia Li
Department of Hematology, The First Hospital of Jilin University
13 shared publicationsXin Wan
Department of Hematology, The First Hospital of Jilin University
12 shared publications
Latest Publications
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S7 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Univariate and Multivariable Analysis of PFS in Overall
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S7 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Univariate and Multivariable Analysis of PFS in Overall
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Figure S1 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Kaplan–Meier survival curves comparing CR and non-CR patients by disease subtype
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Kaplan–Meier survival curves comparing CR and non-CR patients by disease subtype
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S6 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Univariate and Multivariate Logistic Regression Analysis of CR in Overall
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S6 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Univariate and Multivariate Logistic Regression Analysis of CR in Overall
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S1 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Sites of CNS and other tissue involvement in SCNSL patients
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S1 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Sites of CNS and other tissue involvement in SCNSL patients
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S3 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Prior and Glofitamab Treatments
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S3 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Prior and Glofitamab Treatments
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S2 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S4 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Characteristics and Response of patients with glofitamab monotherapy or combination therapy
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S4 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Characteristics and Response of patients with glofitamab monotherapy or combination therapy
- Open Access
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Table S5 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Characteristics in CR and non-CR patients
- 3 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S5 from Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Characteristics in CR and non-CR patients
- Open Access
- 13 August 2026
- Published by Wiley in American Journal of Hematology
- Vol. 101 (S3) , 50-64
Development and Validation of a Novel Geriatric Risk Score for Prognostication in Older Patients With Hodgkin Lymphoma: A Multicenter Retrospective Study
Outcomes in older patients with Hodgkin lymphoma (HL) are compromised by the interplay of patient frailty and disease aggressiveness; however, current stratification tools, including the International Prognostic Score (IPS) and Comprehensive Geriatric Assessment (CGA), lack sufficient prognostic discrimination in the older HL population. We developed and validated a prognostic model integrating metabolic tumor burden and geriatric assessment. In this retrospective study across 14 centers in China between 2006 and 2024, we enrolled 306 patients aged ≥ 60 years with histologically confirmed HL. Patients were randomly partitioned into training ( n = 250) and validation ( n = 56) cohorts. Among the 306 patients, 98 deaths and 130 progression events were recorded during follow‐up. We analyzed 21 candidate variables. The least absolute shrinkage and selection operator (LASSO) analysis and multivariable Cox regression identified five independent predictors for 5‐year overall survival (OS): age > 73 years, baseline 18F‐FDG PET/CT‐derived total lesion glycolysis (TLG) > 200, hemoglobin ≤ 101 g/L, activities of daily living (ADL) dependence, and lymphocyte‐depleted classical Hodgkin lymphoma (LDCHL). A weighted Geriatric Risk Score stratified patients into low‐, intermediate‐, and high‐risk groups. In the validation cohort, the Geriatric Risk Score showed higher discriminatory accuracy than the CGA for both OS (C‐index, 0.770 [95% CI, 0.674–0.867] vs. 0.671 [0.581–0.762]) and PFS (0.761 [0.668–0.853] vs. 0.635 [0.535–0.735]). Among advanced‐stage (Ann Arbor stage III–IV) patients, it also outperformed the IPS‐7 and IPS‐3. By integrating metabolic tumor burden and geriatric assessment, the Geriatric Risk Score improves risk stratification over existing tools in older patients with HL.
- 13 August 2026
- Published by Wiley in American Journal of Hematology
- Vol. 101 (S3) , 50-64
Open AccessDevelopment and Validation of a Novel Geriatric Risk Score for Prognostication in Older Patients With Hodgkin Lymphoma: A Multicenter Retrospective Study
Outcomes in older patients with Hodgkin lymphoma (HL) are compromised by the interplay of patient frailty and disease aggressiveness; however, current stratification tools, including the International Prognostic Score (IPS) and Comprehensive Geriatric Assessment (CGA), lack sufficient prognostic discrimination in the older HL population. We developed and validated a prognostic model integrating metabolic tumor burden and geriatric assessment. In this retrospective study across 14 centers in China between 2006 and 2024, we enrolled 306 patients aged ≥ 60 years with histologically confirmed HL. Patients were randomly partitioned into training ( n = 250) and validation ( n = 56) cohorts. Among the 306 patients, 98 deaths and 130 progression events were recorded during follow‐up. We analyzed 21 candidate variables. The least absolute shrinkage and selection operator (LASSO) analysis and multivariable Cox regression identified five independent predictors for 5‐year overall survival (OS): age > 73 years, baseline 18F‐FDG PET/CT‐derived total lesion glycolysis (TLG) > 200, hemoglobin ≤ 101 g/L, activities of daily living (ADL) dependence, and lymphocyte‐depleted classical Hodgkin lymphoma (LDCHL). A weighted Geriatric Risk Score stratified patients into low‐, intermediate‐, and high‐risk groups. In the validation cohort, the Geriatric Risk Score showed higher discriminatory accuracy than the CGA for both OS (C‐index, 0.770 [95% CI, 0.674–0.867] vs. 0.671 [0.581–0.762]) and PFS (0.761 [0.668–0.853] vs. 0.635 [0.535–0.735]). Among advanced‐stage (Ann Arbor stage III–IV) patients, it also outperformed the IPS‐7 and IPS‐3. By integrating metabolic tumor burden and geriatric assessment, the Geriatric Risk Score improves risk stratification over existing tools in older patients with HL.