← Back to all signals
RESEARCH PAPER ANALYSIS

Benmelstobart plus anlotinib versus pembrolizumab as first-line treatment for PD-L1-positive, advanced non-small-cell lung cancer (CAMPASS): a blinded, randomised, controlled, phase 3 trial.

AI interpretation is pending for this paper.

Open original publication →
PMID41825453
JournalThe Lancet. Oncology
Publication Date2026-03-10
Ingested2026-08-02 12:06 AM
EXECUTIVE SUMMARY

What the AI sees

Not AI summarized yet.

WHY IT MATTERS

Research significance

Pending deeper interpretation.

ABSTRACT

Source abstract

BACKGROUND: PD-1 and PD-L1 inhibitors have been shown to synergise with anti-angiogenic agents in non-small-cell lung cancer (NSCLC). We aimed to compare benmelstobart plus anlotinib with pembrolizumab in patients with previously untreated, driver gene-negative, PD-L1-positive, advanced NSCLC. METHODS: The blinded, randomised, controlled, phase 3 CAMPASS trial was conducted in 79 centres across China. Patients aged 18-75 years with stage IIIB-IV squamous or non-squamous NSCLC, no previous systemic treatment for advanced, recurrent or metastatic diseases, a PD-L1 tumour proportion score of 1% or greater, a life expectancy of 3 months or longer, at least one measurable lesion, and an Eastern Cooperative Oncology Group performance status of 0 or 1 were randomly assigned (2:1) to receive intravenous benmelstobart (1200 mg once on day 1) plus oral anlotinib (12 mg daily on days 1-14) or intravenous pembrolizumab (200 mg once on day 1) plus placebo every 3 weeks. Randomisation was done centrally and stratified by tumour histology, PD-L1 tumour proportion score, and brain metastases. Treatment allocation was open label for investigators and masked to patients and statisticians. The primary endpoint was progression-free survival as assessed by a blinded independent review committee per Response Evalutation Criteria in Solid Tumours version 1.1 in the intention-to-treat population (all randomly assigned patients). Safety was assessed in all randomly assigned patients who received at least dose of study drug. Results reported here are from a preplanned final analysis for progression-free survival. This ongoing study is closed to recruitment and is registered with ClinicalTrials.gov, NCT04964479. FINDINGS: Between Aug 6, 2021, and Dec 14, 2022, 531 patients were randomly assigned (354 to the benmelstobart plus anlotinib group and 177 to the pembrolizumab plus placebo group). 449 (85%) patients were male, 82 (15%) were female, and 493 (93%) were of Han ethnicity. Two patients in the benmelstobart plus anlotinib group and one patients in the pembrolizumab plus placebo group were untreated and therefore excluded from the safety population. After a median follow-up of 11·4 months (95% CI 9·4-13·1) for the benmelstobart plus anlotinib group and 10·6 months (9·0-13·0) for the pembrolizumab plus placebo group, median progression-free survival was 11·0 months (9·2-12·6) and 7·1 months (5·8-9·5), respectively (hazard ratio [HR] 0·70 [95% CI 0·54-0·90]; log-rank p=0·0057). Grade 3 or worse treatment-related adverse events occurred in 206 (59%) of 352 patients in the benmelstobart plus anlotinib group and 51 (29%) of 176 patients in the pembrolizumab plus placebo group, and the most frequent one was hypertension (90 [26%] vs five [3%]). Serious treatment-related adverse events occurred in 89 (25%) patients in the benmelstobart plus anlotinib group and 37 (21%) patients in the pembrolizumab plus placebo group, the most common of which were haemoptysis (nine [3%] vs none) and immune-mediated pulmonary diseases (eight [2%] vs five [3%]). Five (1%) treatment-related deaths occurred in the benmelstobart plus anlotinib group (two due to haemoptysis and one each due to immune-mediated pulmonary disease, disease progression, and infection pneumonia) and four (2%) occurred in the pembrolizumab plus placebo group (one each due to respiratory failure, pulmonary inflammation, disease progression, and myocardial injury). INTERPRETATION: Benmelstobart plus anlotinib showed longer progression-free survival than pembrolizumab plus placebo and no unexpected safety signals were reported, suggesting benmelstobart plus anlotinib as a potential first-line option in driver gene-negative, PD-L1-positive, advanced NSCLC. Longer term follow-up is needed to establish effects on overall survival. FUNDING: Chia Tai Tianqing Pharmaceutical Group.

SUPPORTING PAPER SET

32 more papers to review

Ranked by current scoring engine
1 Incidence rates of non-Hodgkin lymphoma subtypes among Black Africans with and without HIV in South Africa: a national registry-based study. The Lancet regional health. Africa 67.9 2 Primary extranodal marginal zone lymphoma of gastric mucosa-associated lymphoid tissue in children: a case report and review of the literature. Journal of medical case reports 57.4 3 Neurofibromatosis Type 1: An Imaging Review of Multisystem Manifestations in Children. Journal of neuroimaging : official journal of the American Society of Neuroimaging 58.4 4 Reconstructive Strategies for Abdominal Wall Defects in Patients With Stomas: A Systematic Review of Mesh and Flap Techniques. Cureus 74.5 5 Landscape of cancer genomics and precision oncology in Japan, South Korea, China, and Australia. The Lancet regional health. Western Pacific 57.0 6 Deep learning segmentation of the cerebral ventricular system and brainstem for pediatric radiotherapy planning. Physics and imaging in radiation oncology 71.94 7 Real-world clinical outcomes and safety of anlotinib-containing regimens in pediatric solid tumors: a retrospective cohort study at a Chinese center. Frontiers in oncology 72.2 8 Regression of severe sclerotic chronic graft-versus-host disease after a second haploidentical hematopoietic stem cell transplantation: a case report. Frontiers in medicine 62.2 9 Editorial: Advances in the diagnosis and treatment of pediatric hematological disorders. Frontiers in pediatrics 50.74 10 Disability pension receipt five years after cancer diagnosis: a matched registry study of working-age cancer survivors in Norway. Frontiers in health services 64.0 11 Early discontinuation vs. continuation of empirical antibiotics in patients with cancer and febrile neutropenia: a systematic review and meta-analysis of randomized controlled trials. Frontiers in microbiology 82.0 12 Novel juxtamembrane FLT3 in-frame insertion in a child with refractory AML: a case report of durable remission following allogeneic HSCT and FLT3 inhibitor therapy. Frontiers in oncology 64.48 13 Case Report: Pallister-Hall syndrome diagnosed in adulthood during evaluation of recurrent hypoglycemia. Frontiers in endocrinology 49.0 14 Efficacy and safety of immunotherapy in pediatric malignant brain tumors: a systematic review and exploratory meta-analysis. Frontiers in oncology 84.42 15 Case Report: DICER1 mutation-associated anaplastic sarcoma of the kidney in a child. Frontiers in oncology 49.9 16 Epstein-Barr virus and hepatic failure: pathogenesis, clinical manifestations, and management. Frontiers in immunology 62.0 17 Fibrous hamartoma of infancy: a case report. Frontiers in pediatrics 49.9 18 ST6Gal2 promotes α2,6-sialylation and aggressive phenotypes in neuroblastoma cells. bioRxiv : the preprint server for biology 66.8 19 Prevalence and genotype distribution of human papillomavirus (HPV) among adolescent girls and young women in a high HIV burden rural area of South Africa: a cross-sectional survey. Research square 61.0 20 Language of Hope in Conversations between Pediatric Oncologists, Children with Advanced Cancer, and their Families. Research square 57.6 21 Fifteen-year surveillance of non-typhoidal Salmonella bloodstream infections in a tertiary care hospital in southern Türkiye. Journal of infection in developing countries 67.0 22 Understanding the Immune Response Changes to Clinical Interventions for Epstein-Barr Virus Infection Prior to Lymphoma Development in Children After Organ Transplants (UNEARTH). Pediatric transplantation 81.52 23 White matter-cognition mapping in pediatric cancer survivors: a two-cohort NODDI-Bingham study. bioRxiv : the preprint server for biology 71.9 24 Transcriptomic analysis reveals differential regulation of synaptic components in pediatric and adult brain tumors. bioRxiv : the preprint server for biology 61.1 25 Odontogenic myxoma of the mandibular angle in a pediatric patient: a rare clinical entity - case report. International journal of surgery case reports 49.9 26 Adult-onset primary retroperitoneal cystic lymphangioma displacing the inferior vena cava: laparoscopic management of a triple-rarity case from Nepal and review of recent literature. International journal of surgery case reports 57.5 27 Isolated supernumerary nipple along embryonic milk line in an adult male patient successfully treated by surgical excision: a case report. International journal of surgery case reports 49.9 28 Jejunal mesenteric cyst presenting as acute midgut volvulus in a child: a rare cause of surgical abdomen. International journal of surgery case reports 58.0 29 Langerhans cell histiocytosis presenting as a cecal mass in an adolescent: a rare surgical case report. International journal of surgery case reports 51.4 30 An unusual lead point: jejunal leiomyosarcoma causing jejuno-jejunal intussusception - a case report. International journal of surgery case reports 56.3 31 Heterotopic pancreas as a rare lead point of ileal intussusception mimicking acute appendicitis in a child: a case report and review of the literature. International journal of surgery case reports 49.0 32 The vertebral axis in retroperitoneal fetus in fetu: a case report on the definitive diagnosis. International journal of surgery case reports 49.9
PATIENT-FRIENDLY SUMMARY

Benmelstobart plus anlotinib versus pembrolizumab as first-line treatment for PD-L1-positive, advanced non-small-cell lung cancer (CAMPASS): a blinded, randomised, controlled, phase 3 trial.

For education only—not personal medical advice.

Before you continue

AI-assisted research information

Neurocompute uses AI to summarize scientific papers, interpret research signals, and suggest relevant reference links. AI-generated content can be incomplete, misleading, or wrong, and generated links may be irrelevant or unavailable.

Our reviewed outputs have performed strongly to date, but past accuracy is not a guarantee. Verify summaries, scores, claims, and links against the original publication before relying on them.

This platform is for research and education only. It does not provide medical advice, diagnosis, treatment recommendations, or clinical guidance.

Pediatric cancer research intelligence graphic
PEDIATRIC CANCER VISUAL SYSTEM

Open the Research Intelligence Map

Explore the active pediatric oncology analysis view.

Expand Intelligence View →
Full Pediatric cancer research intelligence graphic