Evidence map›Paper›PMID 41818162›Full record

Trial reportCA: a cancer journal for clinicians

Aumolertinib with carboplatin-pemetrexed versus aumolertinib for nonsmall cell lung cancer with EGFR and concomitant tumor suppressor genes (ACROSS2): An open-label, multicenter, randomized phase 3 study.

Jian-Chun Duan, Jia Zhong, Bo-Yang Sun, Wen-Hua Zhao, Lin Wu, Kai-Lun Fei, Qian Chu, Qi-Sen Guo, Qi-Bin Song, Yan Yu and 16 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in CA: a cancer journal for clinicians. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04500717 (Almonertinib Alone Versus Almonertinib Plus Chemotherapy as First-Line Treatment in Locally Advanced Or Metastatic NSCLC Patients With Concomitant EGFR and Tumor Suppressor Gene Mutation), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04500717 phase3unknown statusnot on this map

Almonertinib Alone Versus Almonertinib Plus Chemotherapy as First-Line Treatment in Locally Advanced Or Metastatic NSCLC Patients With Concomitant EGFR and Tumor Suppressor Gene Mutation: A Multicenter, Open-Label, Randomized, Controlled Phase III Study (ACROSS2)

TypeinterventionalSponsorCancer Institute and Hospital, Chinese Academy of Medical SciencesRan2020 to 2023Enrolled460ConditionsNon Small Cell Lung CancerArmsAlmonertinib, Almonertinib plus carboplatin and pemetrexed
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Targeting ClassicalCancers · 2026
    Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Jian-Chun DuanState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0003-3300-1707
Jia ZhongState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0002-0464-3754
Bo-Yang SunState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0001-9529-7932
Wen-Hua ZhaoDepartment of Respiratory Oncology, Guangxi Medical University Cancer Hospital, Nanning, China.ORCID https://orcid.org/0009-0004-6468-6635
Lin WuThe Department of Thoracic Medical Oncology, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.ORCID https://orcid.org/0000-0001-7078-7767
Kai-Lun FeiState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0002-6813-9362
Qian ChuDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0001-8192-7630
Qi-Sen GuoDepartment of Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Jinan, China.ORCID https://orcid.org/0009-0009-5193-5475
Qi-Bin SongCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0002-4350-0916
Yan YuDepartment of Respiratory Oncology, Harbin Medical University Cancer Hospital, Harbin, China.ORCID https://orcid.org/0000-0001-5598-763X
Da-Xing ZhuLung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID https://orcid.org/0009-0004-1916-3122
Xin-Yan LiuDepartment of Oncology, Hebei Chest Hospital, Shijiazhuang, China.ORCID https://orcid.org/0000-0003-0481-9104
Jun ZhaoDepartment of Thoracic Oncology, Beijing Cancer Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-1464-7158
Zhi-Xiang ZhanDepartment of Oncology, Xinyang Central Hospital, Xinyang, China.ORCID https://orcid.org/0009-0008-0410-8648
Shi LiDepartment of Oncology, Shenyang Chest Hospital, Shenyang, China.ORCID https://orcid.org/0009-0004-2973-9885
Lei NieDepartment of Oncology, Shanxi Provincial Cancer Hospital, Xian, China.ORCID https://orcid.org/0009-0004-4052-5511
Jie LinDepartment of Oncology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID https://orcid.org/0000-0003-3784-8120
Xiao-Dong PengDepartment of Oncology, Chengdu Second People's Hospital, Chengdu, China.ORCID https://orcid.org/0009-0009-1806-4145
Dian-Sheng ZhongDepartment of Oncology, Tianjin Medical University General Hospital, Tianjin, China.ORCID https://orcid.org/0000-0001-6483-8134
Jin ZhouDepartment of Oncology, Sichuan Cancer Hospital, Chengdu, China.ORCID https://orcid.org/0000-0001-9984-7137
Li-Hua LiDepartment of Oncology, The First People's Hospital of Yunnan Province, Kunming, China.ORCID https://orcid.org/0009-0009-9797-1308
Yun-Fang ChenDepartment of Oncology, Zhumadian Central Hospital Affiliated to Huanghuai University, Zhumadian, China.ORCID https://orcid.org/0009-0003-9034-8878
Chen HuDivision of Quantitative Sciences, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-4672-1981
Tony MokState Key Laboratory of Translational Oncology, Department of Clinical Oncology, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.ORCID https://orcid.org/0000-0002-8251-0551
Zhi-Jie WangState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0002-7722-4956
Jie WangState Key Laboratory of Molecular Oncology, Beijing Key Laboratory, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0002-5602-0487

Funding

National High Level Hospital Clinical Research Funding 2025-LYZX-D-A01National Natural Science Foundation of China 82272796National Natural Science Foundation of China 82303969The Noncommunicable Chronic Diseases-National Science and Technology Major Project 2024ZD0519700The Noncommunicable Chronic Diseases-National Science and Technology Major Project 2024ZD0520200The Noncommunicable Chronic Diseases-National Science and Technology Major Project 2024ZD0520202
6 · The paper itself

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.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarboplatinCarcinoma, Non-Small-Cell LungLung NeoplasmsPemetrexedAdultAgedErbB ReceptorsFemaleHumansMaleMiddle AgedMutationProgression-Free SurvivalProspective StudiesCarboplatinEGFR protein, humanErbB ReceptorsPemetrexedaumolertinibconcomitant tumor suppressor gene mutationsEGFR mutationnonsmall cell lung cancer

Identifiers

PMID41818162
PMCPMC12981368

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.