Evidence map›Paper›PMID 30679316›Full record

Trial reportThe oncologist2019

Phase II Study of the Triple Combination Chemotherapy of SOXIRI (S-1/Oxaliplatin/Irinotecan) in Patients with Unresectable Pancreatic Ductal Adenocarcinoma.

Takahiro Akahori, Masayuki Sho, Hiroaki Yanagimoto, Sohei Satoi, Minako Nagai, Satoshi Nishiwada, Kenji Nakagawa, Kota Nakamura, Tomohisa Yamamoto, Satoshi Hirooka and 2 more

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

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 24 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

12 authors at 2 institutions in 1 country.

Takahiro AkahoriDepartment of Surgery, Nara Medical University, Nara, Japan.
Masayuki ShoDepartment of Surgery, Nara Medical University, Nara, Japan akahorin@naramed-u.ac.jp.
Hiroaki YanagimotoDepartment of Surgery, Kansai Medical University, Osaka, Japan.
Sohei SatoiDepartment of Surgery, Kansai Medical University, Osaka, Japan.
Minako NagaiDepartment of Surgery, Nara Medical University, Nara, Japan.
Satoshi NishiwadaDepartment of Surgery, Nara Medical University, Nara, Japan.
Kenji NakagawaDepartment of Surgery, Nara Medical University, Nara, Japan.
Kota NakamuraDepartment of Surgery, Nara Medical University, Nara, Japan.
Tomohisa YamamotoDepartment of Surgery, Kansai Medical University, Osaka, Japan.
Satoshi HirookaDepartment of Surgery, Kansai Medical University, Osaka, Japan.
So YamakiDepartment of Surgery, Kansai Medical University, Osaka, Japan.
Naoya IkedaDepartment of Surgery, Nara Medical University, Nara, Japan.
Nara Medical University · JPKansai Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

lessons learnedThe triple combination chemotherapy of SOXIRI (S-1/oxaliplatin/irinotecan) in patients with unresectable pancreatic ductal adenocarcinoma was an effective treatment that appeared to be better tolerated than the widely used FOLFIRINOX regimen.SOXIRI regimen may provide an alternative approach for advanced pancreatic cancer.

backgroundIn our previous phase I study, we determined the recommended dose of a biweekly S-1, oxaliplatin, and irinotecan (SOXIRI) regimen in patients with unresectable pancreatic ductal adenocarcinoma (PDAC). This phase II study was conducted to assess the safety and clinical efficacy in patients with unresectable PDAC.

methodsPatients with previously untreated metastatic and locally advanced PDAC were enrolled. The primary endpoint was response rate (RR). Secondary endpoints were adverse events (AEs), progression-free survival (PFS), and overall survival (OS). Patients received 80 mg/m

resultsThirty-five enrolled patients received a median of six (range: 2-15) treatment cycles. The RR was 22.8% (95% confidence interval [CI]: 10.4-40.1); median OS, 17.7 months (95% CI: 9.8-22.0); and median PFS, 7.4 months (95% CI: 4.2-8.4). Furthermore, the median OS in patients with distant metastasis was 10.1 months, whereas that in patients with locally advanced PDAC was 22.6 months. Major grade 3 or 4 toxicity included neutropenia (54%), anemia (17%), febrile neutropenia (11%), anorexia (9%), diarrhea (9%), and nausea (9%). There were no treatment-related deaths.

conclusionSOXIRI is considered a promising and well-tolerated regimen in patients with unresectable PDAC.

Indexed as

AdenocarcinomaAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalCohort StudiesDrug CombinationsFemaleFollow-Up StudiesHumansIrinotecanMaleMiddle AgedOxaliplatinOxonic AcidPancreatic NeoplasmsDrug CombinationsIrinotecanOxaliplatinOxonic AcidS 1 (combination)Tegafur

Identifiers

PMID30679316
PMCPMC6656520
OpenAlexW2914606580

What OpenQuestion holds

Textmetadata
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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.