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Profil bibliographique

Hong‐Hong Yan

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

237Publications signalées
7773Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Lung Cancer Treatments and MutationsLung Cancer Diagnosis and TreatmentLung Cancer Research StudiesCancer Immunotherapy and BiomarkersCancer Genomics and Diagnostics

Les publications récentes

2026 conference-abstract OpenAlex

Abstract PS5-02-16: Clinical outcomes and treatment attrition rates of HER2 positive metastatic breast cancer (MBC) patients at a tertiary referral cancer centre in London: the Guy’s Cancer experience

Hong‐Hong Yan, M. Toki, Hartmut Kristeleit

Abstract Background: Treatment options for HER2 positive MBC are increasing and trastuzumab deruxtecan (T-DXd) is now used in earlier lines of treatment, having shown superiority to trastuzumab emtansine (T-DM1) in DESTINY-Breast03 and to THP in DESTINY-Breast09. Uncertainty remains on the optimal sequencing …

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0 citations Clinical Cancer Research
Accès ouvert 2025 article OpenAlex

Comparing the efficacy and safety of the ABC-14 regimen (azacitidine, venetoclax, and chidamide) with traditional “3 + 7” intensive induction regimen or AB-14 regimen (venetoclax combined with azacitidine) in newly diagnosed AML: study protocol for a prospective, multicenter, randomized, open-label clinical trial

Hong‐Hong Yan, Xin Li Huang, Ping Wu, Chengxin Deng et autres

BACKGROUND: Induction therapy is the first critical step in the overall treatment of Acute myeloid leukemia (AML). The "3 + 7" regimen remains the backbone treatment for newly diagnosed AML patients suitable for intense chemotherapy (IC). However, its efficacy, toxicity, high complications …

cn (code pays fourni par la source)

0 citations Trials
Accès ouvert 2025 article OpenAlex

Cellular dynamics in cerebrospinal fluid unveils the key regulators of intracranial response to immune checkpoint inhibitors in NSCLC brain metastases

Yang-Si Li, Wenpu Lai, Kai Yin, Hai‐Yan Tu et autres

Background Brain metastases (BrM) in non-small cell lung cancer (NSCLC) present a significant challenge due to poor prognosis. While immune checkpoint inhibitors (ICIs) have been standard treatments for NSCLC, their efficacy in BrM is variable, emphasizing the urgent need for predictive biomarkers …

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2 citations Journal for ImmunoTherapy of Cancer
2025 conference-abstract OpenAlex

Molecular profiling of neoadjuvant immunochemotherapy and identification of residual cancer cells in pCR NSCLC: A single-cell analysis of CTONG 1804 clinical trial.

SiYang Maggie Liu, Song Dong, Xue‐Ning Yang, Ri-Qiang Liao et autres

8025 Background: Previously, we reported the clinical findings of stage-one enrollment from a phase II trial of neoadjuvant immunochemotherapy (IO) in untreated patients with resectable non-small cell lung cancer (NSCLC) (CTONG1804, NCT04015778). Recently, two-stage enrollment has been completed. This trial provided an …

cn (code pays fourni par la source)

0 citations Journal of Clinical Oncology
Accès ouvert 2025 supplementary-materials OpenAlex

Supplementary Figure S3 from Follow-up Analysis Enhances Understanding of Molecular Residual Disease in Localized Non–Small Cell Lung Cancer

Jia‐Tao Zhang, Si‐Yang Liu, Xuan Gao, Si‐Yang Maggie Liu et autres

Supplementary Figure S3. (A) Kaplan–Meier analysis of disease-free survival (DFS) stratified by landmark MRD status for LUAD patients. (B) Kaplan–Meier analysis of DFS stratified by longitudinal MRD status for LUAD patients. (C) Kaplan-Meier analysis of the survival time since last blood, comparing …

0 citations
Accès ouvert 2025 supplementary-materials OpenAlex

Supplementary Figure S4 from Follow-up Analysis Enhances Understanding of Molecular Residual Disease in Localized Non–Small Cell Lung Cancer

Jia‐Tao Zhang, Si‐Yang Liu, Xuan Gao, Si‐Yang Maggie Liu et autres

Supplementary Figure S4. Kaplan-Meier analysis of the survival time since last blood, comparing patients with longitudinal undetectable MRD to those with longitudinal detectable MRD (last blood draw positive), excluding synchronous recurrences.

0 citations

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