Evidence map›Paper›PMID 39392339›Full record

Observational studyCancer research communications2024

Association between Immune-Related Adverse Events and Atezolizumab in Previously Treated Patients with Unresectable Advanced or Recurrent Non-Small Cell Lung Cancer.

Hidetoshi Hayashi, Makoto Nishio, Hiroaki Akamatsu, Yasushi Goto, Satoru Miura, Akihiko Gemma, Ichiro Yoshino, Toshihiro Misumi, Takashi Kijima, Naoto Takase and 10 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cancer research communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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. Observational
  2. Review
  3. 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

20 authors.

Hidetoshi HayashiDepartment of Medical Oncology, Faculty of Medicine, Kindai University, Osaka, Japan.ORCID 0000-0001-8787-5587
Makoto NishioDepartment of Thoracic Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID 0000-0003-4969-4165
Hiroaki AkamatsuInternal Medicine III, Wakayama Medical University, Wakayama, Japan.ORCID 0000-0001-5856-5512
Yasushi GotoDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-7437-5054
Satoru MiuraDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.ORCID 0000-0001-7868-6661
Akihiko GemmaDepartment of Pulmonary Medicine and Oncology, Nippon Medical School, Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0003-0762-2737
Ichiro YoshinoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID 0009-0003-4007-9606
Toshihiro MisumiDepartment of Biostatistics, Yokohama City University School of Medicine, Kanagawa, Japan.ORCID 0000-0001-8339-2895
Takashi KijimaDepartment of Respiratory Medicine and Hematology, Hyogo Medical University, School of Medicine, Hyogo, Japan.ORCID 0000-0003-4249-4021
Naoto TakaseDepartment of Medical Oncology, Takarazuka City Hospital, Hyogo, Japan.ORCID 0009-0005-6484-7301
Masaki FujitaDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.ORCID 0000-0003-1209-1272
Sadatomo TasakaDepartment of Respiratory Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.ORCID 0000-0003-4861-4143
Atsuto MouriDepartment of Respiratory Medicine, International Medical Center, Saitama Medical University, Saitama, Japan.ORCID 0000-0001-8704-8151
Tetsuro KondoDepartment of Thoracic Oncology, Kanagawa Cancer Center, Kanagawa, Japan.ORCID 0000-0003-4388-4814
Kei TakamuraDepartment of Respiratory Medicine, Obihiro-Kosei General Hospital, Hokkaido, Japan.ORCID 0000-0003-2707-5355
Yosuke KawashimaDepartment of Pulmonary Medicine, Sendai Kousei Hospital, Miyagi, Japan.ORCID 0000-0002-9824-6572
Kazuyoshi ImaizumiDepartment of Respiratory Medicine, Fujita Health University School of Medicine, Toyoake, Japan.ORCID 0000-0002-3790-8691
Shunichiro IwasawaChugai Pharmaceutical Co., Ltd., Tokyo, Japan.ORCID 0009-0000-1366-9676
Shintaro NakagawaChugai Pharmaceutical Co., Ltd., Tokyo, Japan.ORCID 0009-0000-8433-6801
Tetsuya MitsudomiKindai Hospital Global Research Alliance Center and Thoracic Surgery, Kindai University, Osaka, Japan.ORCID 0000-0001-9860-8505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeReal-world, large-scale studies on the association between immune-related adverse events (irAE) and immune checkpoint inhibitor therapy effectiveness are limited. We evaluated overall survival (OS) and progression-free survival based on the occurrence and grade of irAEs. PATIENTS AND

methodsWe used data from Japanese patients with unresectable advanced or recurrent non-small cell lung cancer (NSCLC) who received atezolizumab and were enrolled in J-TAIL, a multicenter, prospective, single-arm observational study.

resultsAmong the 1,002 patients, 190 (19.0%) developed irAEs. The most common irAEs were skin disorders (3.8%) of any grade and interstitial lung disease (1.5%) of grade ≥3. Patients who developed irAEs within 4 or 6 weeks of treatment initiation had higher baseline C-reactive protein levels than those without irAEs. OS was longer in patients with irAEs [HR, 0.66; 95% confidence interval (CI), 0.54-0.82], particularly in those with low-grade irAEs (HR, 0.45; 95% CI, 0.33-0.62), than in patients without irAEs. The HR (95% CI) for OS in patients with low-grade and high-grade skin or endocrine disorder-related irAEs was 0.42 (0.28-0.64) and 0.37 (0.15-0.88), respectively. The HR (95% CI) for OS in patients with low-grade and high-grade irAEs other than skin or endocrine disorders was 0.44 (0.30-0.65) and 1.27 (0.96-1.69), respectively.

conclusionsIn patients with unresectable advanced or recurrent NSCLC treated with atezolizumab in real-world settings, irAEs are associated with a clinical benefit except in those with high-grade irAEs other than skin and endocrine disorders. SIGNIFICANCE: Immune checkpoint inhibitors are useful for treating NSCLC but can cause life-threatening irAEs. This study had a large sample size and stratified the analysis by irAE type and grade. The results suggest that improved management of irAEs may improve the therapeutic effect of atezolizumab.

Indexed as

Antibodies, Monoclonal, HumanizedCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalProgression-Free SurvivalProspective StudiesAntibodies, Monoclonal, HumanizedatezolizumabImmune Checkpoint Inhibitors

Identifiers

PMID39392339
PMCPMC11528261

What OpenQuestion holds

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Registered trials

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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.