Evidence map›Paper›PMID 37675546›Full record

ArticleThoracic cancer2023

Phase II study of IRInotecan treatment after COmbined chemo-immunotherapy for extensive-stage small cell lung cancer: Protocol of IRICO study.

Hiromi Tomono, Hirokazu Taniguchi, Minoru Fukuda, Takaya Ikeda, Seiji Nagashima, Kazumasa Akagi, Sawana Ono, Yasuhiro Umeyama, Midori Shimada, Hiroshi Gyotoku and 13 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

23 authors at 7 institutions in 1 country.

Hiromi TomonoDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.ORCID 0009-0006-2748-9418
Hirokazu TaniguchiDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.ORCID 0000-0003-2414-8344
Minoru FukudaClinical Oncology Center, Nagasaki University Hospital, Nagasaki, Japan.ORCID 0000-0002-5321-1843
Takaya IkedaDepartment of Respiratory Medicine, National Hospital Organization Nagasaki Medical Center, Nagasaki, Japan.
Seiji NagashimaDepartment of Respiratory Medicine, National Hospital Organization Nagasaki Medical Center, Nagasaki, Japan.
Kazumasa AkagiDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Sawana OnoDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Yasuhiro UmeyamaDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Midori ShimadaDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Hiroshi GyotokuDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Shinnosuke TakemotoDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.ORCID 0000-0003-0373-0618
Yasushi HisamatsuDepartment of Thoracic Medical Oncology, Oita Prefectural Hospital, Oita, Japan.
Ryotaro MorinagaDepartment of Thoracic Medical Oncology, Oita Prefectural Hospital, Oita, Japan.
Ryuta TagawaDepartment of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.
Ryosuke OgataDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Yosuke DotsuDepartment of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.
Hiroaki SenjuDepartment of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.
Hiroshi SodaDepartment of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.ORCID 0000-0003-4993-1837
Katsumi NakatomiDepartment of Respiratory Medicine, National Hospital Organization Ureshino Medical Center, Saga, Japan.
Fumiko HayashiDepartment of Respiratory Medicine, Nagasaki Prefecture Shimabara Hospital, Nagasaki, Japan.
Nanae SugasakiDepartment of Respiratory Medicine, Nagasaki Prefecture Shimabara Hospital, Nagasaki, Japan.
Akitoshi KinoshitaDepartment of Respiratory Medicine, Nagasaki Prefecture Shimabara Hospital, Nagasaki, Japan.
Hiroshi MukaeDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Nagasaki University · JPSasebo City General Hospital · JPNagasaki Prefectural Shimabara High School · JPNagasaki Medical Center · JPNagasaki University Hospital · JPOita Prefectural Hospital · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCombined treatment using anti-programmed death-ligand 1 antibody (anti-PD-L1) and platinum-etoposide is the current standard first-line treatment for patients with extensive-stage (ES) small cell lung cancer (SCLC). However, the best treatment for relapsed ES-SCLC after the first-line treatment remains unclear. There are some approved chemotherapeutic agents that can be used against ES-SCLC, and treatment with irinotecan is well established as both a monotherapy and a combined therapy, in combination with platinum. Therefore, we conduct a phase II study with irinotecan in the second- or later-line setting for patients with ES-SCLC who have been previously treated with combined treatment.

methodsOur study will enroll total 30 patients who are diagnosed with ES-SCLC and have experienced disease progression after the combined treatment. Patients will receive irinotecan on days 1, 8, and 15, which will be repeated every 4 weeks. Doses of irinotecan (100/80/60 mg/m DISCUSSION: Since the present first-line treatment has been changed to the combined treatment, the second- or later-line treatment should be re-evaluated for patients with relapsed SCLC. Irinotecan is a major chemotherapeutic agent used for SCLC. This study demonstrates and re-evaluates the clinical benefits of irinotecan after combined treatment with anti-PD-L1 and platinum-etoposide for patients with ES-SCLC. REGISTRATION DETAILS: This study was registered in the Japan Registry of Clinical Trials (no. jRCT s071210090) on November 4, 2021.

Indexed as

Lung NeoplasmsSmall Cell Lung CarcinomaAntineoplastic Combined Chemotherapy ProtocolsCamptothecinCisplatinClinical Trials, Phase II as TopicDisease ProgressionEtoposideHumansImmunotherapyIrinotecanNeoplasm Recurrence, LocalPlatinumCamptothecinCisplatinEtoposideIrinotecanPlatinumcombined chemo-immunotherapyirinotecansmall cell lung cancer

Identifiers

PMID37675546
PMCPMC10542459
OpenAlexW4386503155

What OpenQuestion holds

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LicenceCC BY
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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.