- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group, Focus V (anlotinib) / Advenchen
Biomarker, Journal, PD(L)-1 Biomarker, IO biomarker: ERBB2 I655V mutation correlates with efficacy of immunotherapy in gallbladder cancer. (Pubmed Central) - Mar 7, 2026 Moreover, the radiomics nomogram is a valuable tool for refining patient selection and advancing personalized treatment strategies for individuals with uHCC. The ERBB2 I655V mutation may be associated with improved treatment response to immunotherapy in gallbladder cancer.
- |||||||||| zeprumetostat (SHR-2554) / Treeline Biosci
Journal: Zeprumetostat: First Approval. (Pubmed Central) - Mar 7, 2026 1 line of systemic therapy. This article summarizes the milestones in the development of zeprumetostat leading to this first approval for the treatment of r/r PTCL.
- |||||||||| Journal, PD(L)-1 Biomarker, IO biomarker: Recent highlights and breakthroughs in immunotherapy for head and neck cancers. (Pubmed Central) - Mar 6, 2026
Lipo-IRI may be a good option as a component of standard second-line for patients with relapsed/metastatic colorectal cancer. Recent advances highlight a rapid surge in positive immunotherapy trials across different head and neck cancer entities, with clinical benefit observed both when immune checkpoint inhibitors are moved earlier in the disease course and when they are combined with agents targeting resistance mechanisms or enabling more precise drug delivery to tumors.
- |||||||||| Review, Journal, Benefit-risk assessment: First-Line Serplulimab versus Other Anti-PD-1/PD-L1 Antibodies Plus Chemotherapy for Esophageal Squamous Cell Carcinoma: A Systematic Review with Benefit-Risk Assessment via Matching-Adjusted Indirect Comparison. (Pubmed Central) - Mar 6, 2026
The pooled adjusted PFS HR was 0.91 (95% CI, 0.81-1.02), significantly favoring serplulimab over nivolumab (HR, 0.56; 95% CI, 0.33-0.96), with favorable trends versus pembrolizumab (HR, 0.83; 95% CI, 0.63-1.10) and sugemalimab (HR, 0.86; 95% CI, 0.63-1.16)...This indirect comparison provides comparative benefit-risk evidence to inform first?line treatment selection for locally advanced or metastatic ESCC. Serplulimab plus chemotherapy demonstrated a clinically meaningful PFS benefit, comparable OS after matching, and a manageable safety profile consistent with the PD-1/PD-L1 inhibitor class.
- |||||||||| FROM FEASIBILITY TO FINDINGS: SUPPORTING INDIRECT TREATMENT COMPARISONS WITH GENERATIVE AI () - Mar 6, 2026 - Abstract #ISPOR2026ISPOR_1397;
Bayesian NMA results showed significant overall survival benefits for sintilimab plus bevacizumab (HR 0.38; 95% CrI 0.21-0.79), camrelizumab plus rivoceranib (HR 0.42; 0.21-0.82), and atezolizumab plus bevacizumab (HR 0.45; 0.23-0.87) compared with placebo. GenAI can streamline ITC workflows by supporting feasibility assessment, analysis planning, and result interpretation, and when combined with standard NMA tools and expert review enhances efficiency while preserving rigor and enabling faster evidence generation for HTA and JCA use cases.
- |||||||||| Do SGLT2 Inhibitors Influence Parkinson's Disease Risk? A Meta-analysis of Randomized Trials (McCormick Place West | Hall F; In-Person; Virtual) - Mar 5, 2026 - Abstract #AAN2026AAN_4436;
Building on its efficacy advantages, trastuzumab rezetecan offers a novel therapeutic option for HER2-mutant NSCLC patients, thereby enhancing their overall health outcomes. No eligible data were found for ertugliflozin, enavogliflozin, henagliflozin, ipragliflozin, luseogliflozin, or tofogliflozin...Subgroup analyses showed no significant effect for individual agents: empagliflozin 10 mg (OR 0.64, 95% CI 0.17
- |||||||||| SHR-1819 / Jiangsu Hengrui Pharma
Trial completion, Enrollment change: A Study to Extend Efficacy and Safety of SHR-1819 Injection in Adult Patients With Moderate to Severe Atopic Dermatitis (clinicaltrials.gov) - Mar 5, 2026 P2, N=79, Completed, No eligible data were found for ertugliflozin, enavogliflozin, henagliflozin, ipragliflozin, luseogliflozin, or tofogliflozin...Subgroup analyses showed no significant effect for individual agents: empagliflozin 10 mg (OR 0.64, 95% CI 0.17 Enrolling by invitation --> Completed | N=240 --> 79
- |||||||||| remimazolam tosylate (HR-7056) / Jiangsu Hengrui Pharma
Trial completion, Trial completion date, Trial primary completion date: Application of Low-dose Muscle Relaxants in Bronchoscopic Interventional Procedures (clinicaltrials.gov) - Mar 4, 2026 P=N/A, N=153, Completed, The combination of adebrelimab, bevacizumab, and cisplatin/carboplatin was the first regimen to demonstrate promising intracranial antitumor activity and prolonged PFS and CNS-PFS, along with a manageable safety profile, warranting further investigation. Recruiting --> Completed | Trial completion date: Jan 2028 --> Jul 2025 | Trial primary completion date: Jun 2026 --> Jul 2025
- |||||||||| Aqupla (nedaplatin) / Simcere, AiRuiKa (camrelizumab) / Elevar Therapeutics
A Unique Case of Multiple Primary Lung Cancer With Three Distinct Histological Tumor Subtypes and Different Gene Mutations (W314 (Level III, OCCC West Concourse); Poster Board # 720) - Mar 3, 2026 - Abstract #ATS2026ATS_8520; Patient received four cycles of postoperative adjuvant chemotherapy [Docetaxel + Nedaplatin]...Six cycles of adjuvant chemotherapy [Etoposide+ Nedaplatin] and five cycles of immunotherapy [Camrelizumab] were administered postoperatively...Genetic results reveal completely different origins, and potentially treatment options for various lesions. Smoking is a risk factor for MPLC, but additional mechanistic research is required.
- |||||||||| Comparative Efficacy of Targeted Therapies for Moderate-to-Severe Atopic Dermatitis without Topical Corticosteroids: an updated network meta-analysis () - Mar 2, 2026 - Abstract #AAD2026AAD_2675;
Objective: To compare the relative efficacy of targeted systemic therapies (Dupilumab, Stapokibart, Tralokinumab, Lebrikizumab, Nemolizumab, Upadacitinib, Abrocitinib, Baricitinib, Ivarmacitinib) for moderate-to-severe AD without topical corticosteroids through network meta-analysis... Among targeted therapies for moderate-to-severe AD without concomitant topical TCS for 12 or 16 weeks, upadacitinib 30 mg demonstrated the most efficacious in this NMA.
- |||||||||| AiRuiLi (adebrelimab) / Jiangsu Hengrui Pharma
Adebrelimab plus chemotherapy for extensive-stage small-cell lung cancer: A real-world study (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2071; For safety analysis, one patient experienced grade 3 intestinal obstruction, and two patients experienced grade 2 hepatic dysfunction. [Conclusions] In real-world settings, adebrelimab combined with chemotherapy showed promising efficacy and acceptable safety for treating ES-SCLC.
- |||||||||| AiRuiLi (adebrelimab) / Jiangsu Hengrui Pharma
Adebrelimab plus chemotherapy as first-line treatment for ES-SCLC: A real-world retrospective study (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2066; The most common adverse event was myelosuppression, observed in 12 patients (63.2%) of any grade, including grade ?3 in 3 patients (15.8%). [Conclusions] In real-world settings, adebrelimab combined with chemotherapy demonstrated encouraging efficacy and acceptable safety as a first-line treatment for ES-SCLC.
- |||||||||| First-Line Treatment Recommended by the Chinese National Guidelines for Primary Liver Cancer: A Network Meta-Analysis (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2050;
Compared to sorafenib, atezolizumab + bevacizumab, camrelizumab + apatinib, and donafenib significantly reduced mortality additionally, compared to lenvatinib, both atezolizumab + bevacizumab and camrelizumab + apatinib demonstrated survival benefit. [Conclusions] Camrelizumab + apatinib may offer the most favorable PFS and OS among first-line therapies currently recommended in the Chinese guidelines for liver cancer.
- |||||||||| First-Line Systemic Therapies for Hepatocellular Carcinoma with MVI and EHS: A Network Meta-Analysis (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2040;
The top three ranked treatment regimens for overall survival benefit were Camrelizumab plus apatinib (41.3%), Sintilimab plus bevacizumab biosimilar (36.3%), and Atezolizumab plus bevacizumab (19.1%). [Conclusions] For HCC with MVI and EHS, Camrelizumab plus apatinib may be considered the preferred first-line treatment option.
- |||||||||| AiRuiKa (camrelizumab) / Elevar Therapeutics
Camrelizumab plus chemotherapy achieved long-term survival in advanced non-small cell lung cancer: A case series (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2023; Treatment switched to camrelizumab, albumin-bound paclitaxel, and carboplatin for five cycles, followed by 37 cycles of camrelizumab plus anlotinib...Case 4 A patient with lung adenocarcinoma started camrelizumab, pemetrexed, and carboplatin in February 2023, followed by maintenance with pemetrexed plus camrelizumab...Conclusions Camrelizumab plus chemotherapy yielded long-term survival in some advanced NSCLC patients in real-world practice. Further studies are needed to elucidate the mechanisms driving these responses.
- |||||||||| Tevimbra (tislelizumab-jsgr) / BeOne Medicines, Tyvyt (sintilimab) / Innovent Biologics, Eli Lilly, AiRuiKa (camrelizumab) / Elevar Therapeutics
Immune Checkpoint Inhibitor Plus Chemotherapy as First-Line Treatment for Squamous NSCLC: A Network Meta-Analysis (Poster venue | Pacifico Yokohama Exhibition Hall D) - Mar 2, 2026 - Abstract #JSMO2026JSMO_2018; probabilities of OS benefit from sintilimab plus chemotherapy and camrelizumab plus chemotherapy as first-line treatments for sqNSCLC were similar. [Conclusions] Considering the PFS and OS benefits of camrelizumab plus chemotherapy as first-line treatment for sqNSCLC, it may be regarded as a preferred therapeutic option.
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