Evidence map›Paper›PMID 36751477›Full record

ArticleGastroenterology report2023

Oxaliplatin plus irinotecan vs irinotecan as second-line treatment in pancreatic cancer patients: a randomized-controlled open-label Phase II study.

Hangyu Zhang, Zhou Tong, Lulu Liu, Qihan Fu, Xudong Zhu, Xiaomeng Dai, Xuanwen Bao, Weijia Fang, Yi Zheng, Peng Zhao

Open access · diamondAbstract read
In one paragraph

Article in Gastroenterology report, 2023. 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, top 71% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

10 authors at 1 institution in 1 country.

Hangyu ZhangDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Zhou TongDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Lulu LiuDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Qihan FuDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Xudong ZhuDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Xiaomeng DaiDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Xuanwen BaoDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Weijia FangDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Yi ZhengDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.
Peng ZhaoDepartment of Medical Oncology, School of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, P. R. China.ORCID https://orcid.org/0000-0002-5479-899X
First Affiliated Hospital Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Limited second-line therapeutic options are available for metastasis pancreatic cancer (mPC). We aimed to explore the efficacy and safety of oxaliplatin plus irinotecan (IROX) in mPC patients. Methods: This is an open-label, Phase 2, randomized study of mPC patients (aged 18-75 years) who failed when using gemcitabine plus S-1 as first-line therapy. Block randomization with a block size of four was used to randomly assign patients (1:1) between October 2015 and December 2017 to receive either IROX (oxaliplatin 85 mg/m Results: A total of 74 patients were enrolled in this study, including 44 males and 30 females, with an average age of 61 years. The median overall survival was 10.2 and 6.7 months (adjusted hazard ratio [HR], 0.7; 95% confidence interval [CI], 0.4-1.2; Conclusions: IROX had no significant survival benefit over irinotecan monotherapy in our study. However, IROX reduced the risk of disease progression by 60%, with acceptable toxicity.

Indexed as

irinotecanIROXpancreatic cancerrandomized control trialsecond-line chemotherapy

Identifiers

PMID36751477
PMCPMC9897170
OpenAlexW4319078758

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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.