Core Viewpoint - Junshi Biosciences (君实生物) announced that its product JS207, a recombinant humanized anti-PD-1 and VEGF bispecific antibody, has received FDA approval for a clinical trial in patients with resectable, AGA-negative non-small cell lung cancer [1] Group 1: Product Information - JS207 is a self-developed bispecific antibody targeting PD-1 and VEGFA, primarily used for the treatment of advanced malignancies [1] - The drug binds with high affinity to both PD-1 and VEGFA, effectively blocking the interaction between PD-1 and PD-L1/PD-L2, as well as inhibiting the binding of VEGF to its receptors [1] - JS207 exhibits both immunotherapeutic and anti-angiogenic properties, neutralizing VEGF to inhibit endothelial cell proliferation, improve the tumor microenvironment, and enhance the infiltration of cytotoxic T lymphocytes in the tumor microenvironment, leading to better anti-tumor activity [1] Group 2: Clinical Trial Details - The clinical trial is an open-label, two-arm, randomized, positive-controlled Phase II/III study comparing JS207 to Nivolumab for neoadjuvant treatment [1] - The study focuses on patients with resectable, AGA-negative non-small cell lung cancer [1]

Core Viewpoint - The article narrates the journey of a family dealing with a cancer diagnosis, highlighting the emotional and medical challenges faced by the family as they seek treatment options for the mother diagnosed with duodenal adenocarcinoma and multiple liver metastases. Group 1: Diagnosis and Initial Findings - The mother, previously healthy, was diagnosed with duodenal adenocarcinoma with multiple liver metastases after a routine health check-up revealed a 4.7 cm lesion on the liver [4][5][8] - Initial assessments indicated no surgical options available due to the extent of the disease [4][10] Group 2: Diagnostic Journey - The family sought further evaluations, leading to a series of tests including ultrasound and MRI, which confirmed the presence of malignant lesions [6][8][20] - Tumor markers showed elevated CA199 levels at 736, indicating a poor prognosis [7][8] Group 3: Treatment Options and Decisions - The family explored treatment options, including participation in clinical trials for chemotherapy and targeted therapy [14][27] - The mother expressed a desire for a PET CT scan to assess the extent of metastasis, which revealed a primary tumor in the duodenum with liver metastases [17][19] Group 4: Pathological Confirmation - Biopsy results confirmed the diagnosis of duodenal cancer with liver metastases, leading to a revised treatment plan [22][25] Group 5: Treatment Strategy - The treatment plan included a combination of chemotherapy and targeted therapy, with the potential for surgery if the tumor responded well [27][28] - The family joined a support group that provided valuable information and emotional support during the treatment process [28][29] Group 6: Surgical Considerations - After successful chemotherapy, the mother was evaluated for surgical options, with a focus on minimizing risks associated with the complex surgery [39][56] - The surgical team emphasized the importance of thorough imaging to guide the surgical approach, leading to a decision to proceed with surgery [49][50] Group 7: Surgical Outcome - The surgery was successful, with the removal of both the primary tumor and liver metastases, and pathology indicated no active disease in the liver [59][60] - Post-operative recovery was complicated by fever and other issues, but the medical team remained optimistic about the mother's recovery [67][70]