Qiping Zhuo
Research Subjects
Qiping Zhuo has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Kainan Wang
Department of Oncology, The Second Hospital of Dalian Medical University, 116023 Dalian, Liaoning, China
1 shared publication - Man Li
Department of Oncology, the Second Hospital of Dalian Medical University
1 shared publication - Xiaomeng Jia
Department of Oncology, The Second Hospital of Dalian Medical University, Dalian, 116023, China
1 shared publication - Xueqing Wang1 shared publication
Latest Publications
- Open Access
- 21 October 2025
- Published by Wolters Kluwer Health in Annals of Medicine & Surgery
- Vol. 87 (12) , 8540-8548
Optimizing endocrine adjuvant therapy in HR+/HER2− breast cancer: supplemental strategies and innovations
Endocrine therapy (ET) is a cornerstone in adjuvant therapy for hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2−) breast cancer. However, recent research challenges the conventional 5-year adjuvant therapy duration. Patients with T1N0M0 HR+/HER2− breast cancer face a 13% risk of distant recurrence after 5 years of endocrine treatment. This risk increases to 34% over two decades for patients with 4–9 lymph node metastases. Thus, it is important to consider supplementary treatments for T1N0M0 HR+/HER2− breast cancer patients, particularly those with additional high-risk features such as young age, high tumor grade, or adverse genomic profile. We summarize intensive treatment methods for T1N0M0 HR+/HER2− breast cancer patients, which extend beyond the standard 5-year tamoxifen (TAM)-based adjuvant ET. These methods include intensive ET, poly(ADP-ribose) polymerase (PARP) inhibitors, other targeted therapies, antibody-drug conjugates, oral chemotherapy, immunotherapy, and enhanced prevention of bone metastasis. This review provides a foundation for developing personalized adjuvant treatment strategies for patients with T1N0M0 HR+/HER2− breast cancer.
- 21 October 2025
- Published by Wolters Kluwer Health in Annals of Medicine & Surgery
- Vol. 87 (12) , 8540-8548
Open AccessOptimizing endocrine adjuvant therapy in HR+/HER2− breast cancer: supplemental strategies and innovations
Endocrine therapy (ET) is a cornerstone in adjuvant therapy for hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2−) breast cancer. However, recent research challenges the conventional 5-year adjuvant therapy duration. Patients with T1N0M0 HR+/HER2− breast cancer face a 13% risk of distant recurrence after 5 years of endocrine treatment. This risk increases to 34% over two decades for patients with 4–9 lymph node metastases. Thus, it is important to consider supplementary treatments for T1N0M0 HR+/HER2− breast cancer patients, particularly those with additional high-risk features such as young age, high tumor grade, or adverse genomic profile. We summarize intensive treatment methods for T1N0M0 HR+/HER2− breast cancer patients, which extend beyond the standard 5-year tamoxifen (TAM)-based adjuvant ET. These methods include intensive ET, poly(ADP-ribose) polymerase (PARP) inhibitors, other targeted therapies, antibody-drug conjugates, oral chemotherapy, immunotherapy, and enhanced prevention of bone metastasis. This review provides a foundation for developing personalized adjuvant treatment strategies for patients with T1N0M0 HR+/HER2− breast cancer.