Evidence map›Paper›PMID 38165684›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2024

Phase II Study of Durvalumab Immediately after Completion of Chemoradiotherapy in Unresectable Stage III Non-small Cell Lung Cancer: TORG1937 (DATE Study).

Shinji Nakamichi, Kaoru Kubota, Toshihiro Misumi, Tetsuro Kondo, Shuji Murakami, Yoshimasa Shiraishi, Hisao Imai, Daijiro Harada, Kazutoshi Isobe, Hidetoshi Itani and 10 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 17 institutions in 1 country.

Shinji NakamichiDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.ORCID 0000-0002-2298-6945
Kaoru KubotaDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.ORCID 0000-0003-0367-2606
Toshihiro MisumiDepartment of Biostatistics, Yokohama City University School of Medicine, Yokohama, Japan.ORCID 0000-0001-8339-2895
Tetsuro KondoDepartment of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.ORCID 0000-0003-4388-4814
Shuji MurakamiDepartment of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.ORCID 0000-0001-5104-5493
Yoshimasa ShiraishiDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0001-5015-193X
Hisao ImaiDivision of Respiratory Medicine, Gunma Prefectural Cancer Center, Ota, Japan.ORCID 0000-0003-3097-4255
Daijiro HaradaDepartment of Thoracic Oncology and Medicine, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.ORCID 0000-0002-5314-2489
Kazutoshi IsobeDepartment of Respiratory Medicine, Toho University Omori Medical Center, Tokyo, Japan.ORCID 0000-0002-9995-2217
Hidetoshi ItaniDepartment of Respiratory Medicine, Japanese Red Cross Ise Hospital, Ise, Japan.ORCID 0009-0006-2007-4666
Saori TakataDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.ORCID 0009-0002-5010-7212
Hiroshi WakuiDivision of Respiratory Diseases, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.ORCID 0000-0002-3729-1716
Yuki MisumiDepartment of Respiratory Medicine and Medical Oncology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan.ORCID 0000-0001-9633-9268
Satoshi IkedaDepartment of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.ORCID 0000-0001-5203-7911
Tetsuhiko AsaoDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-9975-2282
Naoki FuruyaDepartment of Internal Medicine, Division of Respiratory Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0001-7162-5946
Shinobu HosokawaDepartment of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama, Japan.ORCID 0000-0001-5645-2434
Yumiko KobayashiDepartment of Pulmonary Medicine, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.ORCID 0009-0009-0322-1494
Yuichi TakiguchiDepartment of Medical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0001-6059-7476
Hiroaki OkamotoDepartment of Respiratory Medicine and Medical Oncology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan.ORCID 0000-0003-3110-5545
Kanagawa Prefectural Hospital Organization · JPNippon Medical School · JPYokohama Municipal Citizen's Hospital · JPChiba University · JPIse Red Cross Hospital · JPJikei University School of Medicine · JPJuntendo University · JPKanagawa Cardiovascular and Respiratory Center · JPKyorin University · JPKyushu University · JPOkayama Red Cross General Hospital · JPSaitama International Medical Center · JPSaitama Medical University · JPShikoku Cancer Center · JPSt. Marianna University School of Medicine · JPToho University · JPYokohama City University · JP

Funding

n/a
6 · The paper itself

Abstract

purposeConcurrent chemoradiotherapy (CCRT) followed by durvalumab consolidation for up to 12 months is the standard of care for patients with unresectable stage III non-small cell lung cancer (NSCLC). However, exactly when to initiate durvalumab therapy after chemoradiation completion remains unknown. We evaluated the efficacy and safety of durvalumab, administered immediately after CCRT completion, for patients with unresectable stage III NSCLC. PATIENTS AND

methodsThis study was a prospective, single-arm, open-label phase II clinical trial. Patients without disease progression after definitive CCRT (two cycles of platinum-based doublet chemotherapy with 60 Gy/30 Fr radiotherapy) received durvalumab (every 2 weeks for up to 12 months) from the next day (up to 5 days) after the final radiation dose. The primary endpoint was the 1-year progression-free survival (PFS) from registration before the start of CCRT.

resultsFrom January 2020 to August 2020, 47 of 50 enrolled patients were evaluable for treatment efficacy and safety. The 1-year PFS from registration was 75.0% [60% confidence interval (CI), 69.0-80.0 and 95% CI, 59.4-85.3]. The objective response rate throughout the study treatment and median PFS from registration were 78.7% and 14.2 months (95% CI, 13.4 to not reached), respectively. Grade 3/4 pneumonitis and febrile neutropenia were each 4.3%.

conclusionsOur study met the primary endpoint. The incidence of pneumonitis was similar to that of a Japanese subset in the PACIFIC study. Our data support the efficacy and safety of durvalumab administered immediately after the completion of CCRT for patients with unresectable stage III NSCLC.

Indexed as

Antibodies, MonoclonalCarcinoma, Non-Small-Cell LungLung NeoplasmsPneumoniaChemoradiotherapyHumansNeoplasm StagingProspective StudiesAntibodies, Monoclonaldurvalumab

Identifiers

PMID38165684
PMCPMC10940851
OpenAlexW4390511706

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.