Evidence map›Paper›PMID 40011378›Full record

Observational studyInternational journal of clinical oncology2025

A multicenter prospective observational study for health assessment questionnaires EQ-5D-5L and G8 in unresectable advanced pancreatic cancer treated with first-line gemcitabine plus nab-paclitaxel therapy.

Kaori Hino, Tomohiro Nishina, Mitsuhito Koizumi, Kaori Marui, Masahito Kokubu, Yuki Numata, Yoshiki Imamura, Kozue Kanemitsu-Okada, Toru Otsuru, Taira Kuroda and 8 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in International journal of clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kaori HinoDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Tomohiro NishinaDepartment of Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, 160 Kou, Minami-Umemoto, Matsuyama, Ehime, 791-0280, Japan. nishina.tomohiro.nj@mail.hosp.go.jp.ORCID http://orcid.org/0000-0002-4073-3757
Mitsuhito KoizumiDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Kaori MaruiEndoscopy Center, Ehime University Hospital, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Masahito KokubuDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Yuki NumataDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Yoshiki ImamuraDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Kozue Kanemitsu-OkadaDepartment of Gastroenterology, Ehime Prefectural Central Hospital, 83 Kasuga-Machi, Matsuyama, Ehime, 790-0024, Japan.
Toru OtsuruDepartment of Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, 160 Kou, Minami-Umemoto, Matsuyama, Ehime, 791-0280, Japan.
Taira KurodaDepartment of Gastroenterology, Ehime Prefectural Central Hospital, 83 Kasuga-Machi, Matsuyama, Ehime, 790-0024, Japan.
Yoshinori OhnoDepartment of Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, 160 Kou, Minami-Umemoto, Matsuyama, Ehime, 791-0280, Japan.
Akinori AsagiDepartment of Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, 160 Kou, Minami-Umemoto, Matsuyama, Ehime, 791-0280, Japan.
Hideki MiyataDepartment of Gastroenterology, Ehime Prefectural Central Hospital, 83 Kasuga-Machi, Matsuyama, Ehime, 790-0024, Japan.
Tomoyuki YokotaCenter for Liver-Biliary-Pancreatic Diseases, Matsuyama Red Cross Hospital, 1 Bunkyo-Cho, Matsuyama, Ehime, 790-8524, Japan.
Teru KumagiDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Ichinosuke HyodoDepartment of Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, 160 Kou, Minami-Umemoto, Matsuyama, Ehime, 791-0280, Japan.
Yoshio IkedaEndoscopy Center, Ehime University Hospital, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Yoichi HiasaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn chemotherapy for unresectable advanced pancreatic cancer (UPC), the clinical utility of pre-treatment health assessment questionnaires, EuroQoL 5-Dimension 5-Level (EQ-5D-5L) and G8, is unknown. This study aimed to fill this gap.

methodsThis multicenter, prospective, observational study investigated the association of EQ-5D-5L and G8 with the clinical outcomes of first-line gemcitabine plus nab-paclitaxel (GnP) for UPC. Differences in survival were analyzed using the log-rank test, and multivariate analyses were performed using the Cox proportional hazards model.

resultsBetween April 2022 and September 2023, 60 patients were enrolled, and their data were analyzed. When patients were classified into two groups using the median EQ-5D-5L utility value (0.824), progression-free survival (PFS) and overall survival (OS) were significantly longer in patients with high EQ-5D-5L utility values than in those with low utility values (median PFS 7.0 vs. 4.7 months, P < 0.01; median OS 12 vs. 8.0 months, P = 0.023). Such differences were not observed in the EQ-5D-5L Visual Analog Scale or G8 scores. There was no association between the occurrence of severe adverse events and EQ-5D-5L or G8 scores. Multivariate analyses showed that high EQ-5D-5L utility value (≥ 0.824), high albumin (≥ 3.8 g/dl), and low carcinoembryonic antigen (CEA) (< 5.4 ng/mL) were preferable independent efficacy predictors for PFS and also independent prognostic factors for OS.

conclusionPre-treatment EQ-5D-5L utility value, along with albumin and CEA, was an independent efficacy predictor and prognostic factor in patients with UPC treated with first-line GnP. Their usefulness should be validated in future studies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDeoxycytidinePancreatic NeoplasmsAdultAgedAged, 80 and overAlbuminsFemaleGemcitabineHumansMaleMiddle AgedPaclitaxelProspective StudiesQuality of LifeSurveys and Questionnaires130-nm albumin-bound paclitaxelAlbuminsDeoxycytidineGemcitabinePaclitaxelEfficacy predictorEQ-5D-5LG8Prognostic factorUnresectable advanced pancreatic cancer

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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.