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Clinical Research · English Editorial Summary

An antibody-drug conjugate nearly doubled survival in relapsed small cell lung cancer — a world-first phase 3 win for B7-H3

At the 2026 World Conference on Lung Cancer, Professor Wang Jie's team reported ARTEMIS-008: the B7-H3 antibody-drug conjugate risvutatug rezetecan extended median overall survival to 18.5 months versus 10.3 months for topotecan chemotherapy — the first phase 3 trial anywhere to show a survival benefit for a B7-H3-targeted drug.

Original report: 30 September 2026English summary: 8 October 2026Source: Medlive (medlive.cn) physician platformEdited by Wellward China
Cancer Hospital Chinese Academy of Medical SciencesBeijingCancer & TumorsSmall cell lung cancerAntibody-drug conjugateB7-H3WCLC 2026
Source and editorial note: This is an original English summary based on Medlive's Chinese-language interview with Prof. Wang Jie (WCLC 2026 report), published 30 September 2026. It is not a full translation or an independent clinical assessment. The original source is the authority for the underlying report.
The study

A decades-old ceiling in small cell lung cancer

Small cell lung cancer is aggressive: most patients respond to first-line chemotherapy, and most relapse within a year. For relapsed disease the main approved option worldwide has long been topotecan, a chemotherapy that extends survival only modestly and causes significant bone-marrow toxicity. Several drug classes have tried and failed to beat it.

At the presidential symposium of the 2026 World Conference on Lung Cancer in Seoul, on 13 September, Professor Wang Jie — director of the department of medical oncology at the Cancer Hospital, Chinese Academy of Medical Sciences — presented the interim analysis of ARTEMIS-008 as a late-breaking abstract: a randomised phase 3 trial of risvutatug rezetecan, an antibody-drug conjugate targeting B7-H3, against topotecan in relapsed small cell lung cancer.

What the trial found

The multicentre, randomised, open-label phase 3 trial enrolled patients whose disease had progressed during or after platinum chemotherapy. At a median follow-up of 12.2 months, the ADC met its primary endpoint: median overall survival was 18.5 months versus 10.3 months for topotecan, a hazard ratio of 0.46 with high statistical significance.

Key results (interim analysis, BICR-assessed)

Median progression-free survival 7.2 versus 3.0 months (HR 0.33); objective response rate about 58% versus 12.6%; nearly 65% of patients alive beyond one year. Benefit was consistent across predefined subgroups, including platinum-sensitive and platinum-resistant disease and patients with brain metastases. Grade ≥3 treatment-related adverse events were lower in the ADC arm (60.9% vs 78.2%), mostly manageable blood-count effects, with no new safety signals.

Evidence status: interim, open-label, numbers undisclosed

The data are from a prespecified interim analysis of an open-label trial, and the reports reviewed do not disclose the randomised patient count, so the results should be read with those caveats. The sponsor, Hansoh Pharma, filed a marketing application with China's NMPA on 2 September 2026 for this indication, and a global phase 3 trial is roughly one-third enrolled. Overseas rights are held by GSK.

Why it matters

This is the first randomised phase 3 trial anywhere to show an overall survival benefit from a B7-H3-targeted therapy, in a cancer where second-line survival had barely moved in decades. It is also an example of the "developed in China, for the world" pattern: the pivotal evidence was generated in Chinese hospitals first. For patients, the drug is not yet on the market — approval is under review. This summary belongs to the Cancer & Tumors health area and is not treatment advice.