Evidence map›Paper›PMID 33471290›Full record

ArticleInternational journal of clinical oncology2021

The prognostic impact of immune-related adverse events in metastatic renal cell carcinoma patients treated with nivolumab: a real-world multi-institutional retrospective study.

Taigo Kato, Akira Nagahara, Norihiko Kawamura, Wataru Nakata, Tetsuji Soda, Kyosuke Matsuzaki, Koji Hatano, Atsunari Kawashima, Takeshi Ujike, Ryoichi Imamura and 8 more

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Article in International journal of clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

18 authors at 6 institutions in 1 country.

Taigo KatoDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan. kato@uro.med.osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-8681-1407
Akira NagaharaDepartment of Urology, Osaka International Cancer Institute, Chuo-ku, Osaka, 541-8567, Japan.
Norihiko KawamuraDepartment of Urology, Osaka General Medical Center, Sumiyoshi-ku, Osaka, 558-8558, Japan.
Wataru NakataDepartments of Urology, Osaka Rosai Hospital, Sakai, Osaka, 591-8025, Japan.
Tetsuji SodaDepartment of Urology, Osaka Police Hospital, Tenoji-ku, Osaka, 543-0035, Japan.
Kyosuke MatsuzakiDepartment of Urology, National Hospital Organization Osaka National Hospital, Chuo-ku, Osaka, 540-0006, Japan.
Koji HatanoDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Atsunari KawashimaDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Takeshi UjikeDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Ryoichi ImamuraDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Kensaku NishimuraDepartment of Urology, National Hospital Organization Osaka National Hospital, Chuo-ku, Osaka, 540-0006, Japan.
Shingo TakadaDepartment of Urology, Osaka Police Hospital, Tenoji-ku, Osaka, 543-0035, Japan.
Masao TsujihataDepartments of Urology, Osaka Rosai Hospital, Sakai, Osaka, 591-8025, Japan.
Seiji YamaguchiDepartment of Urology, Osaka General Medical Center, Sumiyoshi-ku, Osaka, 558-8558, Japan.
Tetsuya TakaoDepartment of Urology, Osaka General Medical Center, Sumiyoshi-ku, Osaka, 558-8558, Japan.
Kazuo NishimuraDepartment of Urology, Osaka International Cancer Institute, Chuo-ku, Osaka, 541-8567, Japan.
Norio NonomuraDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Motohide UemuraDepartment of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
The University of Osaka · JPOsaka National Hospital · JPOsaka Prefectural Medical Center · JPOsaka Police Hospital · JPOsaka Rosai Hospital · JPOsaka International Cancer Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have shown that immune-related adverse events (irAEs) caused by immune checkpoint inhibitors (ICIs) were correlated with favorable clinical outcome in patients with melanoma. However, in metastatic renal cell carcinoma (mRCC) patients, there have been few reports about the correlation between irAEs and clinical efficacy of anti-programmed cell death protein-1 (PD-1) therapy.

methodsWe retrospectively investigated 160 mRCC patients who started nivolumab monotherapy between September 2016 and July 2019. IrAEs were defined as patients' AEs having a potential immunological basis that required close follow-up, or immunosuppressive therapy. We compared the data of patients who received nivolumab into two groups based on the occurrence of irAEs and assessed clinical efficacy in both groups.

resultsOf all mRCC patients, 47 patients (29.4%) developed irAEs. In patients who developed irAEs, the objective response rate and disease control rate were 38.8% and 77.6%, which were significantly higher when compared to that in patients without irAEs (p = 0.012 and p < 0.001, respectively). Furthermore, the incidence of irAEs was significantly associated with an increase in progression-free survival (PFS) [Hazard ratio (HR) = 0.4867; p = 0.0006] and overall survival (OS) (HR = 0.526; p = 0.0252). Importantly, PFS and OS seemed to be similar in patients who discontinued treatment because of irAEs and in those who did not discontinue because of irAEs (p = 0.36 and p = 0.35, respectively).

conclusionDevelopment of irAEs strongly correlates with clinical benefit for mRCC patients receiving nivolumab monotherapy in real-world settings.

Indexed as

Immune-related adverse eventsNivolumabRenal cell carcinoma

Identifiers

PMID33471290
OpenAlexW3121266104

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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.