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Aumolertinib with carboplatin–pemetrexed versus aumolertinib for nonsmall cell lung cancer with <i>EGFR</i> and concomitant tumor suppressor genes (ACROSS2): An open‐label, multicenter, randomized phase 3 study

CA: A Cancer Journal for Clinicians Jian‐Chun Duan, Jia Zhong, Bo‐Yang Sun et al. Mar 01, 2026 DOI: 10.3322/caac.70071

ABSTRACT Third‐generation epidermal growth factor receptor–tyrosine kinase inhibitors (EGFR‐TKIs) are standard first‐line therapy for advanced, EGFR ‐mutated nonsmall cell lung cancer (NSCLC). However, their benefit is limited in patients who have co‐existing tumor suppressor gene (TSG) mutations, highlighting a need for intensified strategies to improve outcomes. ACROSS2 (ClinicalTrials.gov identifier NCT04500717) is the first prospective, multicenter, randomized phase 3 study to compare the third‐generation EGFR‐TKI aumolertinib in combination with carboplatin–pemetrexed versus aumolertinib monotherapy in patients who had NSCLC with EGFR mutations and concomitant TSG mutations. In total, 126 patients were enrolled and randomly assigned to either combination therapy ( n  = 62) or monotherapy ( n  = 64). The primary end point was median progression‐free survival (PFS). At a median follow‐up of 25.3 months, combination therapy significantly prolonged median PFS compared with monotherapy (19.78 vs 16.53 months; hazard ratio, 0.58; 95% confidence interval, 0.34–0.97). Landmark PFS rates at 12, 18, and 24 months were 78.7% versus 65.3%, 67.2% versus 40.8%, and 41.0% versus 29.9%, respectively. Subgroup analyses demonstrated a clear PFS benefit in patients who had co‐existing tumor protein p53 ( TP53 ) mutations. Grade 3 or greater adverse events occurred in 25.9% of patients who received combination therapy versus 17.2% of those who received monotherapy; no drug‐related deaths were observed. Overall survival data were immature (data maturity, 4%). The ACROSS2 trial provides the first prospective evidence supporting a genotype‐directed, chemotherapy‐targeted intensification approach favoring aumolertinib plus carboplatin–pemetrexed for this molecularly defined population.

Adding carboplatin to sequential taxane–anthracycline neoadjuvant chemotherapy shows improved event‐free and overall survival benefits in premenopausal women with triple‐negative breast cancer

CA: A Cancer Journal for Clinicians Carrie Printz Mar 01, 2026 DOI: 10.3322/caac.70077

Integrating multimodal management and molecular profiling in a patient with BRAF V600E–positive melanoma and brain metastases

CA: A Cancer Journal for Clinicians David Gritsch, Riley M. Fadden, Maura K. Mahar et al. Mar 01, 2026 DOI: 10.3322/caac.70079

Global cancer statistics for children: Two decades of change and projections to 2050

CA: A Cancer Journal for Clinicians Wangzhong Li, Shanzhou Huang, Qiyue Chen et al. Mar 01, 2026 DOI: 10.3322/caac.70069

Abstract Reliable, contemporary estimates of the global childhood cancer burden remain scarce, particularly in the post‐coronavirus disease 2019 (COVID‐19) era. By using data from the Global Burden of Disease 2021 and Global Cancer Observatory 2022 projects, the authors evaluated the childhood cancer burden at global, regional, and national levels, characterizing temporal and projected trends, and analyzed the data according to disparities by geography and socioeconomic development. From 2000 to 2021, the age‐standardized incidence rate (ASIR) and the age‐standardized mortality rate (ASMR) of childhood cancer declined overall (average annual percent change, −0.88 and −2.13, respectively), especially during the COVID‐19 pandemic. During this period, the disparities in childhood cancer burden were mainly concentrated in countries/territories with a lower Sociodemographic Index. In 2022, an estimated 202,164 new cases and 77,182 deaths from childhood cancer occurred worldwide (ASIR and ASMR, 10.3 and 3.9 per 100,000 children, respectively). Countries/territories with higher a Human Development Index (HDI) had a higher incidence (ASIR, 8.0 [low HDI] vs. 15.3 [very high HDI] per 100,000), whereas those with a lower HDI had higher mortality (ASMR, 4.4 [low HDI] vs. 2.8 [very high HDI] per 100,000). Analyses indicated that, by 2050, there will be 204,925 projected new cases and 78,210 deaths globally, with increases only in low HDI countries/territories, exacerbating existing health inequities. Childhood cancer remains a global health challenge, with notable geographic and socioeconomic disparities. These data serve as the impetus for governments and policymakers to prioritize resources and equitable access to interventions, particularly in regions with lower levels of development, while addressing health care vulnerabilities exposed by global crises like the COVID‐19 pandemic.

Improved survival, disparate outcomes contemporaneously define the modern worldwide burden of childhood cancers

CA: A Cancer Journal for Clinicians Matthew R. Kudek, Hao Wang Mar 01, 2026 DOI: 10.3322/caac.70073

PIP4K2C: an emerging fulcrum for multiple diseases

Nature Reviews Drug Discovery Luca Pozzetti, Manjari Mishra, Shirit Einav et al. Mar 01, 2026 DOI: 10.1038/d41573-026-00030-8

TIGIT’s immuno-oncology teachings

Nature Reviews Drug Discovery Asher Mullard Mar 01, 2026 DOI: 10.1038/d41573-026-00031-7

Approvals by the China NMPA in 2025

Nature Reviews Drug Discovery Ran Jing, Xiecheng Zhi, Liming Shao Mar 01, 2026 DOI: 10.1038/d41573-026-00028-2

2025’s FDA approvals by regulatory designations

Nature Reviews Drug Discovery Asher Mullard Mar 01, 2026 DOI: 10.1038/d41573-026-00026-4

PD1 blockers work best when used in the morning, suggests cancer chronotherapy trial

Nature Reviews Drug Discovery Asher Mullard Mar 01, 2026 DOI: 10.1038/d41573-026-00025-5

GSK pays US$2 billion for prophylactic food allergen antibody

Nature Reviews Drug Discovery Asher Mullard Mar 01, 2026 DOI: 10.1038/d41573-026-00024-6

Antibody–lectin chimeras: new checkpoint inhibitors in the toolbox

Nature Reviews Drug Discovery M. Teresa Villanueva Mar 01, 2026 DOI: 10.1038/d41573-026-00023-7

Two-step screen for CARD9 inhibitors

Nature Reviews Drug Discovery Alex Eccleston Mar 01, 2026 DOI: 10.1038/d41573-026-00022-8

Lipid flippase inhibitor tackles drug-resistant fungi

Nature Reviews Drug Discovery Sarah Crunkhorn Mar 01, 2026 DOI: 10.1038/d41573-026-00018-4

Predicting small-molecule–RNA interactions

Nature Reviews Drug Discovery Sarah Crunkhorn Mar 01, 2026 DOI: 10.1038/d41573-026-00021-9

Mapping covalent drug targets

Nature Reviews Drug Discovery Sarah Crunkhorn Mar 01, 2026 DOI: 10.1038/d41573-026-00019-3

Spatiotemporal in vivo protein degradation

Nature Reviews Drug Discovery Sarah Crunkhorn Mar 01, 2026 DOI: 10.1038/d41573-026-00020-w

Olfactory receptor activation overcomes obesity

Nature Reviews Drug Discovery Sarah Crunkhorn Mar 01, 2026 DOI: 10.1038/d41573-026-00015-7

The Biomarkers Consortium: 20 years of advancing precision medicine

Nature Reviews Drug Discovery Amanda Klein, Jeffrey Siegel, Steve Hoffmann et al. Mar 01, 2026 DOI: 10.1038/d41573-025-00187-8

Hunting for biopharma’s innovation sweet spot

Nature Reviews Drug Discovery Asher Mullard Mar 01, 2026 DOI: 10.1038/d41573-026-00011-x