Xiaoqiong Tang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Xiaoqiong Tang has a total of 30 co-authors. Here are the top co-authors by number of shared publications:
- Apeng Yang
Department of Hematology The First Affiliated Hospital of Fujian Medical University Fuzhou China
10 shared publications - Chan Long
17Department of Hematology, The First People’s Hospital of Huizhou City, Huizhou, China
10 shared publications - Chongyang Wu
Lanzhou University Second Hospital 18 Department of Hematology Lanzhou, China
10 shared publications - Danyang Wu
10Department of Hematology, The First Hospital of China Medical University, Shenyang, China
10 shared publications - Fengmin Li
20Department of Hematology, The First Hospital of Qinhuangdao, Qinhuangdao, China
10 shared publications - Hui Zhou
23Department of Lymphoma and Hematology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha, China
10 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
- 11 August 2026
- Published by American Association for Cancer Research (AACR) in Blood Cancer Discovery
- Vol. 7 (6) , 909-920
Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Relapsed or refractory central nervous system lymphoma (R/R CNSL) has limited treatment options. This multicenter retrospective study enrolled 84 consecutive patients with R/R CNSL [median age, 59 years; median of 2.5 prior lines of therapy; 53 primary CNSL (PCNSL) and 31 secondary CNSL (SCNSL)] to evaluate the efficacy and safety profiles of glofitamab therapy. For PCNSL, the objective response rate (ORR) was 88% and complete response rate (CRR) was 59% with glofitamab monotherapy (n = 32) and 100% and 81% with combination therapy (n = 21), respectively. For SCNSL, ORR and CRR were 88% and 75% with glofitamab monotherapy (n = 8) and 91% and 65% with combination therapy (n = 23). At 14.7 months of follow-up, median progression-free survival was 19.5 months for PCNSL and 13.5 months for SCNSL. Cytokine release syndrome occurred in 40% (all grades 1–2) of patients, and immune effector cell–associated neurotoxicity syndrome occurred in 8%. Glofitamab-based therapy demonstrated substantial activity with manageable toxicity in this study, offering a promising treatment paradigm for patients with R/R CNSL. Significance: Effective therapies are urgently needed for R/R CNSL. Glofitamab-based therapy demonstrated high response rates in PCNSL (ORR, 92%; CRR, 68%) and SCNSL (ORR, 90%; CRR, 68%) with manageable toxicity in 84 consecutive, heavily pretreated patients, establishing a promising treatment option for this high-risk population.
- 11 August 2026
- Published by American Association for Cancer Research (AACR) in Blood Cancer Discovery
- Vol. 7 (6) , 909-920
Glofitamab-Based Therapy for Relapsed or Refractory CNS Lymphoma: A Multicenter Retrospective Study
Relapsed or refractory central nervous system lymphoma (R/R CNSL) has limited treatment options. This multicenter retrospective study enrolled 84 consecutive patients with R/R CNSL [median age, 59 years; median of 2.5 prior lines of therapy; 53 primary CNSL (PCNSL) and 31 secondary CNSL (SCNSL)] to evaluate the efficacy and safety profiles of glofitamab therapy. For PCNSL, the objective response rate (ORR) was 88% and complete response rate (CRR) was 59% with glofitamab monotherapy (n = 32) and 100% and 81% with combination therapy (n = 21), respectively. For SCNSL, ORR and CRR were 88% and 75% with glofitamab monotherapy (n = 8) and 91% and 65% with combination therapy (n = 23). At 14.7 months of follow-up, median progression-free survival was 19.5 months for PCNSL and 13.5 months for SCNSL. Cytokine release syndrome occurred in 40% (all grades 1–2) of patients, and immune effector cell–associated neurotoxicity syndrome occurred in 8%. Glofitamab-based therapy demonstrated substantial activity with manageable toxicity in this study, offering a promising treatment paradigm for patients with R/R CNSL. Significance: Effective therapies are urgently needed for R/R CNSL. Glofitamab-based therapy demonstrated high response rates in PCNSL (ORR, 92%; CRR, 68%) and SCNSL (ORR, 90%; CRR, 68%) with manageable toxicity in 84 consecutive, heavily pretreated patients, establishing a promising treatment option for this high-risk population.