Publications by authors named "Hui-yan Luo"

This phase 2/3 trial (NCT04856787) assessed the efficacy and safety of SHR-1701, a bifunctional protein targeting PD-L1 and TGF-β, in combination with BP102 (a bevacizumab biosimilar) and XELOX (capecitabine plus oxaliplatin) as a first-line treatment for unresectable metastatic colorectal cancer (mCRC). In this phase 2 study, a total of 62 patients with untreated, histologically confirmed colorectal adenocarcinoma and no prior systemic therapy for metastatic disease were enrolled. Patients received SHR-1701 (30 mg/kg), bevacizumab (7.

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Colorectal adenomas (CRAs) represent precancerous lesions that precede the development of colorectal cancer (CRC). Regular monitoring of CRAs can hinder the progression into carcinoma. To explore the utility of tissue DNA and circulating cell-free DNA (cfDNA) in early diagnosis of CRC, we retrospectively sequenced paired tissue and plasma samples from 85 patients with conventional CRAs.

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Background: Peritoneal metastasis is the most common metastasis pattern of gastric cancer. Patients with gastric cancer peritoneal metastasis (GCPM) have a poor prognosis and respond poorly to conventional treatments. Recently, immune checkpoint blockade (ICB) has demonstrated favourable efficacy in the treatment of GCPM.

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Anaplastic lymphoma kinase (ALK) fusion-positive colorectal cancer (CRC) is a rare and chemotherapy-refractory subtype that lacks established and effective treatment strategies. Additionally, the efficacy and safety of ALK inhibitors (ALKi) in CRC remain undetermined. Herein, we examined a series of ALK-positive CRC patients who underwent various lines of ALKi treatment.

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  • A clinical trial was conducted to compare the effectiveness and safety of two treatments—cetuximab plus FOLFOXIRI (triplet therapy) and cetuximab plus FOLFOX (doublet therapy)—in RAS/BRAF wild-type colorectal cancer patients who had unresectable liver metastases.
  • The study enrolled 146 patients across seven medical centers in China between April 2018 and December 2022, assessing their objective response rate and other outcomes such as tumor response and survival.
  • Results showed that the response rates were similar between the two treatment groups (84.7% for triplet vs. 79.7% for doublet), indicating no significant difference in efficacy, and the trial also monitored
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  • The study focuses on neoadjuvant and adjuvant immunotherapies for cancer, analyzing their similarities and differences using informatics and extensive literature reviews from 2014 to 2023.
  • It involved a detailed retrospective analysis of 1373 studies, assessing variables like publication volume, citation volume, and connection strength to detect trends and research clusters.
  • Results showed significant growth in neoadjuvant therapies (25.18% annually) compared to adjuvant therapies (6.52%), with emerging research areas identified, particularly around efficacy, safety, and key biomarkers impacting these therapy strategies.
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  • - The CAPability-01 trial studied the effectiveness of combining the PD-1 antibody sintilimab with the HDAC inhibitor chidamide, with or without the VEGF antibody bevacizumab, in patients who have advanced colorectal cancer resistant to chemotherapy.
  • - Results showed that the combination therapy (triplet arm) significantly improved progression-free survival and overall response rates compared to the dual therapy (doublet arm), indicating increased treatment efficacy.
  • - Patients experienced various adverse side effects, with two treatment-related deaths reported; however, the analysis suggested the triplet therapy led to enhanced immune activity in the tumor environment.
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Epstein‒Barr virus (EBV)-associated gastric cancer (GC) manifests an intriguing immunotherapy response. However, the cellular basis for EBV-imprinted tumour immunity and on-treatment response remains undefined. This study aimed to finely characterize the dynamic tumour immune contexture of human EBV (+) GC treated with immunochemotherapy by longitudinal scRNA-seq and paired scTCR/BCR-seq.

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Background: Predictive biomarkers for oesophageal squamous cell carcinoma (ESCC) immunotherapy are lacking, and immunotherapy resistance remains to be addressed. The role of long noncoding RNA (lncRNA) in ESCC immune escape and immunotherapy resistance remains to be elucidated.

Methods: The tumour-associated macrophage-upregulated lncRNAs and the exosomal lncRNAs highly expressed in ESCC immunotherapy nonresponders were identified by lncRNA sequencing and polymerase chain reaction assays.

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  • - Gastric mixed adenoneuroendocrine carcinoma (MANEC) is a complex and aggressive tumor consisting of two types: adenocarcinoma (ACA) and neuroendocrine carcinoma (NEC), but its genetic evolution is not well understood.
  • - Analysis of 101 samples from 33 patients revealed four key mutated genes (TP53, RB1, APC, CTNNB1) and indicated that MANEC tends to have whole-genome doubling, reflecting traits similar to certain other gastric cancers.
  • - The study confirmed that MANEC tumors have a single clonal origin, with NEC components exhibiting more aggressive genetic traits, and it found a sequence of transitions from ACA to NEC, providing new insights into how these tumors
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Background: SHR7390 is a novel, selective MEK1/2 inhibitor. Here, we report results from two phase I trials conducted to evaluate the tolerability, safety and antitumor activity of SHR7390 monotherapy for advanced solid tumors and SHR7390 plus camrelizumab for treatment-refractory advanced or metastatic colorectal cancer (CRC).

Patients And Methods: Patients received SHR7390 alone or combined with fixed-dose camrelizumab (200 mg every 2 weeks) in an accelerated titration scheme to determine the maximum tolerated dose (MTD).

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  • The study investigated the consistency and prognostic value of tumor regression grade (TRG) compared to Response Evaluation Criteria in Solid Tumors (RECIST 1.1) in gastric cancer patients who underwent preoperative treatment.
  • Only 19.6% of patients showed consistent results between the two evaluation methods, indicating a poor agreement between them.
  • TRG was found to be a better predictor of disease-free survival (DFS) and overall survival (OS) than RECIST 1.1, with results showing significant correlations with patient outcomes.
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  • - The study aimed to assess whether adding high-dose vitamin C to the standard chemotherapy (FOLFOX ± bevacizumab) would improve outcomes for patients with metastatic colorectal cancer (mCRC).
  • - Results showed that there was no significant difference in progression-free survival (PFS), overall survival (OS), or response rates between the vitamin C group and the control group, although patients with RAS mutations did experience longer PFS with vitamin C.
  • - Overall, high-dose vitamin C did not provide a clear benefit over standard chemotherapy for mCRC, except potentially for patients with specific genetic mutations (RAS mutation).
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Esophageal squamous cell carcinoma (ESCC) is one of the most life- and health-threatening malignant diseases worldwide, especially in China. Long noncoding RNAs (lncRNAs) have emerged as important regulators of tumorigenesis and tumor progression. However, the roles and mechanisms of lncRNAs in ESCC require further exploration.

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Metabolic inhibition via PFKFB3 inhibition has demonstrated considerable tumor inhibitory effects in various studies; however, PFKFB3 inhibition did not show satisfactory tumor inhibition when used in clinical trials. PFKFB3 is a crucial metabolic enzyme that is highly upregulated in cancer cells and directly affects tumor glycolysis. Here, we showed that PFKFB3 inhibition suppresses tumors in vitro and in vivo in immune-deficient xenografts.

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Background: Although immune checkpoint inhibitor (ICI) is regarded as a breakthrough in cancer therapy, only a limited fraction of patients benefit from it. Cancer stemness can be the potential culprit in ICI resistance, but direct clinical evidence is lacking.

Methods: Publicly available scRNA-Seq datasets derived from ICI-treated patients were collected and analyzed to elucidate the association between cancer stemness and ICI response.

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The genetic basis of colorectal cancer (CRC) and its clinical associations remain poorly understood due to limited samples or targeted genes in current studies. Here, we perform ultradeep whole-exome sequencing on 1015 patients with CRC as part of the ChangKang Project. We identify 46 high-confident significantly mutated genes, 8 of which mutate in 14.

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Background: The number of elderly individuals with diabetes is dramatically increasing. Diabetes is a long-term condition and a noncommunicable disease and requires intensive daily self-management. Understanding of self-management from the patients' perspectives is important to nurses, healthcare providers, and researchers and benefits people by improving their self-management skills.

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Background: Circulating tumor DNA (ctDNA) is a promising diagnostic and prognostic marker for many cancers and has been actively investigated in recent years. Previous studies have already demonstrated the potential use of ctDNA methylation markers in the diagnosis and prognostication of colorectal cancer (CRC). This retrospective study validated the value of methylation biomarker MYO1-G (cg10673833) in CRC diagnosis and disease monitoring using digital droplet PCR (ddPCR), a biomarker selected from our previous study due to its highest diagnostic efficiency.

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  • - This study evaluates the combination of regorafenib and toripalimab in treating colorectal cancer, showing an objective response rate (ORR) of 15.2% and a disease control rate of 36.4% at the recommended phase II dose.
  • - Median progression-free survival (PFS) is 2.1 months and overall survival is 15.5 months, with lower response rates in patients with liver metastases compared to those without (8.7% vs. 30.0%).
  • - Adverse events were common, with 94.9% of patients experiencing grade 1 and 38.5% grade 3 complications, and gut microbiome analysis suggests that higher abundance
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  • The study examines how circulating tumor DNA (ctDNA) sequencing can be used to manage colorectal cancer, focusing on the variation of genetic mutations during treatment.
  • 171 patients with unresectable metastatic colorectal cancer were analyzed through blood samples over time, revealing a significant consistency in RAS/BRAF mutation detection between blood and tissue samples.
  • Results indicate that patients who cleared RAS/BRAF mutations during treatment experienced similar survival rates to those without these mutations, emphasizing the importance of monitoring ctDNA changes for better clinical outcomes.
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Background: Sidedness (right/left) of colorectal cancer (CRC) is essential for treatment. Whether carcinogenesis of tobacco varies by sidedness remains unclear. The present study aims to evaluate the sidedness tendency of cigarette smoking and to explore its impact on prognosis.

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  • * A total of 248 young women (aged ≤50) were enrolled in a randomized, double-blind, placebo-controlled trial, receiving either the aprepitant regimen or a placebo regimen alongside standard anti-nausea medications.
  • * The main outcome measured was the complete response rate, which indicates the percentage of patients who experienced no vomiting or need for rescue medication during the first cycle of chemotherapy.
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