Evidence map›Paper›PMID 32495514›Full record

ArticleThoracic cancer2020

Afatinib + bevacizumab combination therapy in EGFR-mutant NSCLC patients with osimertinib resistance: Protocol of an open-label, phase II, multicenter, single-arm trial.

Nobuaki Kobayashi, Hisashi Hashimoto, Chisato Kamimaki, Ryo Nagasawa, Katsushi Tanaka, Sousuke Kubo, Seigo Katakura, Hao Chen, Nobuyuki Hirama, Ryota Ushio and 12 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 40% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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

22 authors at 3 institutions in 2 countries.

Nobuaki KobayashiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0002-7064-320X
Hisashi HashimotoDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Chisato KamimakiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Ryo NagasawaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Katsushi TanakaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Sousuke KuboDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Seigo KatakuraDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Hao ChenDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Nobuyuki HiramaRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Ryota UshioRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Ayako AokiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Kentaro NakashimaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Shuhei TeranishiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Saki ManabeRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Hiroki WatanabeDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Nobuyuki HoritaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0002-8200-0340
Keisuke WatanabeDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yu HaraDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Masaki YamamotoRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.ORCID 0000-0001-7056-4192
Makoto KudoRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Hongmei PiaoDepartment of Respiratory Medicine, Affiliated Hospital of Yanbian University, Yanji, China.
Takeshi KanekoDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yokohama City University · JPYokohama City University Medical Center · JPYanbian University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAs most patients with epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) develop progressive disease after treatment with osimertinib, it is important to develop more effective treatment options. Afatinib has been shown to be more effective in in vitro studies than osimertinib when used in cancer cell lines containing some specific EGFR mutations. Therefore, afatinib may be an effective solution, especially when used in combination with an anti-VEGF agent such as bevacizumab.

methodsA phase II multicenter, open-label, single-arm trial has been initiated to evaluate the efficacy and safety of afatinib and bevacizumab combination as salvage therapy for EGFR-mutated lung cancer in patients previously treated with osimertinib. The primary endpoint will be the objective response rate (ORR) and secondary endpoints are progression-free survival (PFS), overall survival (OS), disease control rate (DCR), and adverse events (AEs). DISCUSSION: A previous study indicated that afatinib inhibits lung cancer cells with specific EGFR mutations more effectively than other EGFR-TKIs such as osimertinib. Therefore, we expect that combination therapy using afatinib and bevacizumab will be effective in patients previously treated with osimertinib (registration no. jRCTs031190077).

Indexed as

AfatinibAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCarcinoma, Non-Small-Cell LungErbB ReceptorsLung NeoplasmsClinical Trials, Phase II as TopicHumansProgression-Free SurvivalAfatinibBevacizumabErbB ReceptorsAfatinibbevacizumabEGFRnon-small cell lung cancerosimertinib

Identifiers

PMID32495514
PMCPMC7396380
OpenAlexW3029285610

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.