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DRUG CLASS:

VEGFR-3 inhibitor

2d
New P2 trial
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Sulanda (surufatinib)
5d
New P4 trial • Real-world evidence
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Sulanda (surufatinib)
9d
Locoregional gemcitabine plus surufatinib and camrelizumab in FGFR2-non-altered intrahepatic cholangiocarcinoma. (PubMed, Cell Rep Med)
Exploratory analysis indicates that responders show significantly higher tumor PD-L1 expression than non-responders do, with median tumor proportion scores of 8% and 2%, respectively. The study is registered at ClinicalTrials.gov (NCT05236699).
Journal • PD(L)-1 Biomarker • IO biomarker
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PD-L1 (Programmed death ligand 1) • FGFR2 (Fibroblast growth factor receptor 2)
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PD-L1 expression
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gemcitabine • AiRuiKa (camrelizumab) • Sulanda (surufatinib)
22d
PTPN9 dephosphorylates IGF1RY1165/1166 and alleviates IGF1R-mediated resistance to tyrosine kinase inhibitor in cholangiocarcinoma. (PubMed, J Exp Clin Cancer Res)
Increasing evidence suggests that a subset of CCA patients can benefit from multiple tyrosine kinase inhibitors (mTKIs) such as surufatinib...Furthermore, cancer-associated fibroblasts (CAFs) were identified as the major source of IGF1 in CCA microenvironment, essential for IGF1R-driven tumor progression.In summary, the PTPN9-IGF1R axis plays a pivotal role in modulating mTKI sensitivity and tumor progression in CCA. This axis serves as a promising biomarker for identifying potential mTKI beneficiaries and represents a potential therapeutic target to enhance mTKI efficacy and overcome resistance.
Journal
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IGF1 (Insulin-like growth factor 1)
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Sulanda (surufatinib)
1m
A case report: enhanced somatostatin receptor expression in metastatic pancreatic neuroendocrine tumor following everolimus therapy. (PubMed, Front Cell Dev Biol)
From August 2019 to October 2020, he received long-acting octreotide and transarterial chemoembolization (TACE), achieving stable disease...In September 2022, oral surufatinib was initiated but paused in September 2023 due to adverse effects...This case demonstrates that everolimus can induce SSTR re-expression in advanced, SSTR-negative pNETs, offering new therapeutic possibilities. The "induction plus re-evaluation" approach could guide personalized treatment strategies in late-stage pNETs, although further studies are needed to validate this approach.
Journal
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SSTR (Somatostatin Receptor) • SSTR2 (Somatostatin Receptor 2)
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everolimus • Sulanda (surufatinib) • octreotide acetate
1m
Surufatinib plus paclitaxel as second-line therapy for advanced gastric cancer: a single-arm, phase 2 clinical trial. (PubMed, Cell Oncol (Dordr))
Surufatinib plus paclitaxel showed promising efficacy and manageable safety as second-line treatment for advanced gastric cancer, especially in patients who had failed prior immunotherapy.
P2 data • Journal
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HER-2 (Human epidermal growth factor receptor 2)
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HER-2 negative
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paclitaxel • Sulanda (surufatinib)
1m
Exploring the efficacy and safety of famitinib combined with epalrestat and torivirine in the treatment of advanced and recurrent/metastatic cervical cancer (ChiCTR2500111354)
P2, N=90, Not yet recruiting, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine; Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of
New P2 trial
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PD-L1 (Programmed death ligand 1)
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famitinib (SHR 1020) • iparomlimab (QL1604)
1m
New P2 trial
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AiRuiKa (camrelizumab) • famitinib (SHR 1020)
2ms
Study to Assess the Efficacy & Safety of KHK4951 in Patients With Neovascular Age-Related Macular Degeneration (clinicaltrials.gov)
P2, N=180, Active, not recruiting, Kyowa Kirin Co., Ltd. | Recruiting --> Active, not recruiting
Enrollment closed
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Eylea (aflibercept intravitreal)
2ms
Study to Assess the Efficacy & Safety of KHK4951 in Patients With Diabetic Macular Edema (clinicaltrials.gov)
P2, N=150, Active, not recruiting, Kyowa Kirin Co., Ltd. | Recruiting --> Active, not recruiting
Enrollment closed
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Eylea (aflibercept intravitreal)
2ms
New P2 trial
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Fotivda (tivozanib) • sturlimogene erparepvec (RP2)
2ms
Olaparib-Cediranib Hybrid as Dual PARP-VEGFR3 Inhibitor Elicits Antitumor Efficacy: Rational Design, Synthesis, Biological Evaluation and Construction of a Charge Convertible pH Responsive Nanoformulation. (PubMed, Bioorg Chem)
Further, a charge-convertible polymer-based nanoformulation (18-PEG-PLL/DMMA nanoparticles) for targeted drug delivery of 18 was developed. Encouragingly, the nanoformulation demonstrated a cytotoxicity-devoid profile towards normal cells owing to its pH-sensitive behavior and manifested selective cell growth inhibition against solid tumor cells, possibly due to the EPR effect.
Journal
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FLT4 (Fms-related tyrosine kinase 4) • PARP2 (Poly(ADP-Ribose) Polymerase 2)
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Lynparza (olaparib) • Recentin (cediranib)