Evidence map›Paper›PMID 40922529›Full record

Trial reportCancer science2025

Amivantamab Plus Chemotherapy in Japanese Patients With EGFR Exon 20 Insertions NSCLC.

Satoru Kitazono, Akira Ono, Tetsuji Kawamura, Osamu Hataji, Hiroshi Tanaka, Shingo Matsumoto, Naohiro Watanabe, Hiromi Nagashima, Masahide Oki, Michiko Takahashi and 9 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Cancer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04538664 (A Randomized, Open-label Phase 3 Study of Combination Amivantamab and Carboplatin-Pemetrexed Therapy, Compared With Carboplatin-Pemetrexed, in Patients With EGFR Exon 20ins Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT04538664 phase3active not recruitingnot on this map

A Randomized, Open-label Phase 3 Study of Combination Amivantamab and Carboplatin-Pemetrexed Therapy, Compared With Carboplatin-Pemetrexed, in Patients With EGFR Exon 20ins Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

TypeinterventionalSponsorJanssen Research & Development, LLCRan2020 to 2027Enrolled308ConditionsCarcinoma, Non-Small-Cell LungArmsAmivantamab, Pemetrexed, Carboplatin
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Satoru KitazonoDepartment of Medical Affairs, At Janssen Pharmaceutical K.K, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7371-2787
Akira OnoDivision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Tetsuji KawamuraDepartment of Respiratory Medicine, NHO Himeji Medical Center, Hyogo, Japan.
Osamu HatajiRespiratory Center, Matsusaka Municipal Hospital, Mie, Japan.
Hiroshi TanakaDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
Shingo MatsumotoDepartment of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Naohiro WatanabeDepartment of Thoracic Oncology, Aichi Cancer Center Hospital, Aichi, Japan.
Hiromi NagashimaDivision of Pulmonary Medicine, Department of Internal Medicine, Iwate Medical University, Iwate, Japan.
Masahide OkiDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Aichi, Japan.
Michiko TakahashiDepartment of Medical Affairs, Janssen Pharmaceutical K.K, Tokyo, Japan.
Tomoko AnazawaClinical Science Division, Research & Development, Janssen Pharmaceutical K.K, Tokyo, Japan.
Takahiro ShiraiClinical Science Division, Research & Development, Janssen Pharmaceutical K.K, Tokyo, Japan.
Aimi YamashitaDepartment of Statistics & Decision Sciences Janssen JP, Janssen Pharmaceutical K.K, Tokyo, Japan.
Honeylet Wortman-VaynJanssen R&D, Spring House, Pennsylvania, USA.
Archan BhattacharyaJanssen Research & Development, High Wycombe, UK.
Trishala AgrawalJanssen R&D, Spring House, Pennsylvania, USA.
Mahadi BaigJanssen R&D, Spring House, Pennsylvania, USA.
Roland E KnoblauchJanssen R&D, Spring House, Pennsylvania, USA.
Hidetoshi HayashiDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0001-8787-5587

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) exon 20 insertion mutations (EGFR Exon 20ins) are the third most common mutations in non-small cell lung cancer (NSCLC) and are associated with a poorer prognosis and resistance to conventional EGFR-tyrosine kinase inhibitors. This subpopulation analysis of the open-label phase 3 trial (PAPILLION) evaluates the efficacy and safety of amivantamab-chemotherapy versus chemotherapy among Japanese patients with locally advanced or metastatic NSCLC with EGFR Exon 20ins mutation (ClinicalTrials.gov, NCT04538664). Patients were randomized 1:1 to either intravenous amivantamab plus carboplatin/pemetrexed chemotherapy or chemotherapy alone. The primary endpoint was progression-free survival (PFS) by blinded independent central review; the secondary endpoints included objective response rate, duration of response, PFS after first subsequent therapy, overall survival, and safety. The overall population (n = 308) included 34 Japanese patients (amivantamab-chemotherapy, n = 19; chemotherapy, n = 15). Median PFS was 15.5 (95% CI 8.0, NE) months with amivantamab-chemotherapy compared with 5.6 (95% CI 3.0, 7.0) months (HR = 0.22 [0.09, 0.53]) for chemotherapy alone. Improvements in secondary endpoints were also greater in the amivantamab-chemotherapy arm than the chemotherapy arm. The predominant adverse events associated with amivantamab-chemotherapy were reversible hematologic and EGFR-related toxic effects; 2 of 19 patients discontinued all study agents due to treatment-emergent adverse events. Efficacy and safety results in this Japanese subpopulation were consistent with those in the overall population and support the first-line use of amivantamab-chemotherapy in this setting. Early identification of patients with EGFR Exon 20ins mutations, preferably with more sensitive next-generation sequencing-based methods, is important to ensure appropriate patient access to amivantamab-chemotherapy. Trial Registration: ClinicalTrials.gov, NCT04538664.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overAntibodies, BispecificCarboplatinEast Asian PeopleErbB ReceptorsExonsFemaleHumansJapanMaleMiddle AgedamivantamabAntibodies, BispecificCarboplatinEGFR protein, humanErbB ReceptorsPemetrexedamivantamabegfr exon20 insertionepidermal growth factor receptornon‐small cell lung cancerprogression‐free survival

Identifiers

PMID40922529
PMCPMC12580869

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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.