Wenping Wang's research while affiliated with First Affiliated Hospital of China Medical University and other places

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Publications (2)


(A–D) PET/CT showed that there were large hypermetabolic lesions in the right mediastinum, which straddled the anterior, middle and posterior mediastinum, and protruded into the lung field and involved the adjacent pleura. (E) The histology of adenocarcinoma with poor differentiation. (F) ALK (+) IHC using the D5F3 ALK antibody.
(A) Integrative Genomics Viewer snapshot of CCDC85A‐ALK by next‐generation sequencing (NGS). (B) A schematic representation of the CCDC85A‐ALK fusion. Exons 1‐2 (1‐413aa) region of CCDC85A gene and ALK (exon 20), with a hypothetical CCDC85A‐ALK fusion. (C) We used the Coils server (https://embnet.vitalit.ch/software/COILS_form.html) to compare the amino acid sequence of CCDC85A gene to a database of proteins known to form coiled coils and found that the probability of a coiled coil domain at the exons 1‐2 (1‐ 413aa) region of CCDC85A gene being present is almost 100%. The x‐axis represents the position in the protein by amino acid number, and the y‐axis shows how strongly that region is predicted to form a coiled coil domain. ‘Window’ refers to the width of the amino acid ‘Window’ that is scanned at one time.
Significant reduction in the tumour volume was observed by the follow‐up CT scans from 2 weeks to 25 months post‐alectinib therapy. The most recent CT scan showed that the patient's lung tumour was close to disappearing, and he had almost achieved a clinical complete response (CCR).
Lung adenocarcinoma with an uncommon CCDC85A‐ALK fusion responding to alectinib: A case report
  • Article
  • Full-text available

September 2022

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15 Reads

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2 Citations

Journal of Cellular and Molecular Medicine

Journal of Cellular and Molecular Medicine

Jieheng Lin

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Wenping Wang

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[...]

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Yang Cao

A 55‐year‐old Chinese man with a right lung mass and lymph node metastasis (T4N3M0 IIIB) was diagnosed with lung adenocarcinoma after a CT‐guided biopsy. With the wide application of next‐generation sequencing (NGS) in tumour detection, we found a rare CCDC85A‐ALK fusion. The patient received alectinib, which had marked efficacy. This is the first report of a lung adenocarcinoma patient harbouring a new uncommon anaplastic lymphocyte kinase fusion that showed a remarkable response to alectinib. NGS aids in selecting treatment in non‐small cell lung cancer patients.

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(A) In the excised specimen of gastric tumor, a hard region of 5x7cm was observed 6cm from the distal margin. (B) The retinal tissue excised during the operation was 25x13x1.5cm in size. (C–E) Hematoxylin and eosin staining suggested poorly differentiated adenocarcinoma, infiltrating the whole gastric wall (T3), carcinoma infiltration in the nerve bundle, no tumor thrombus in the vascular, no cancer involvement in the distal resection margin, and no cancer metastasis in the omentum tissue. The lymph nodes in the greater curvature of the stomach showed cancer metastasis. (F) Programmed cell death ligand 1 (PD-L1) staining was negative.
PET-CT and follow-up CT images. Arrows indicate tumors. (A) After the patient’s tumor recurred, pre-treatment positron emission tomography (PET)-computed tomography (CT) scan suggested metastatic lesions in the right lower chest wall, invasion of the adjacent peritoneum, and hepatic S4 involvement. Multiple patchy and nodular metastases in peritoneum of abdomen and pelvis. (B) After camrelizumab combined with CAPOX for 6 courses, positron emission tomography (PET)-computed tomography (CT) scan showed that the original metastatic lesions on the right lower chest wall disappeared, and the original multiple metastatic lesions on the peritoneum disappeared. No new tumors were observed in other organs. (C–G) During the period of camrelizumab plus capecitabine as maintenance therapy, regular CT scans suggested that the condition was stable, the original tumor lesions disappeared, and no new tumor lesions were found.
We closely followed the patient’s tumor markers, but unfortunately there were no significant abnormalities and no specific changes in the patient’s tumor markers during the onset and treatment.
Clinical Complete Remission of An Advanced Gastric Adenocarcinoma After Camrelizumab Plus Chemotherapy Followed by Camrelizumab Plus Capecitabine: A Case Report

December 2021

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11 Reads

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1 Citation

We report a rare case of PDL1-negative advanced gastric adenocarcinoma that improved significantly after camrelizumab plus chemotherapy followed by camrelizumab plus capecitabine as first-line therapy. A 65-year-old woman was diagnosed with a gastric adenocarcinoma in 2017 via contrast-enhanced computed tomography (CT) and endoscopic biopsy. She stabilised after preoperative neoadjuvant chemotherapy, surgery, and postoperative adjuvant chemotherapy. In September 2019, positron emission tomography (PET)/CT re-examination suggested a peritoneal metastasis and multiple lymph node metastases. She then received six cycles of camrelizumab plus chemotherapy. PET/CT indicated that the metastatic foci had disappeared and that she had achieved a clinical complete response(CCR). She was followed-up with camrelizumab plus capecitabine (maintenance therapy). At the time of writing, her progression-free survival is more than 14 months and her quality of life is good. Thus, camrelizumab plus chemotherapy is a useful first-line treatment for HER2- and PD-L1-negative advanced gastric adenocarcinoma.