Evidence map›Paper›PMID 37605479›Full record

ArticleCancer science2023

Fibroblast inhibition by tocilizumab enabled gemcitabine/nab-paclitaxel rechallenge for pancreatic cancer.

Shuichi Mitsunaga, Masafumi Ikeda, Hiroshi Imaoka, Mitsuhito Sasaki, Kazuo Watanabe, Akihiro Sato, Kazunori Aoki, Atsushi Ochiai, Mayu Makikawa, Masanobu Nishidate and 7 more

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Cancer science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
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  7. STING-targeted PET imaging: unveiling tumor immunogenicity post-chemotherapy in colorectal cancer.European journal of nuclear medicine and molecular imaging · 2024
    Article
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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

17 authors at 2 institutions in 2 countries.

Shuichi MitsunagaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0001-9496-3278
Masafumi IkedaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-4050-2086
Hiroshi ImaokaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Mitsuhito SasakiDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Kazuo WatanabeDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-1810-5308
Akihiro SatoClinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
Kazunori AokiDivision of Molecular and Cellular Medicine, National Cancer Center, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-1292-3764
Atsushi OchiaiDivision of Biomarker Discovery, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.ORCID https://orcid.org/0000-0001-6857-4009
Mayu MakikawaPharmaceutical Science Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Masanobu NishidatePharmaceutical Science Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Kyoko YamaguchiPharmaceutical Science Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Kimio TeraoPharmaceutical Science Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Noriaki SawadaDiscovery Pharmacology Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Takashi FujitomoDiscovery Technology Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Etsuko FujiiPharmaceutical Science Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Atsuhiko KatoNon-clinical Safety Assessment Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Hiroyuki TsunodaDiscovery Technology Department, Chugai Pharmaceutical Co. Ltd., Tokyo, Japan.
Chugai Pharma (United States) · USNational Cancer Center Hospital East · JP

Funding

Japan Agency for Medical Research and Development JP19ak0101043h0105AJapan Agency for Medical Research and Development JP19ak0101044h0104
6 · The paper itself

Abstract

Interleukin-6 (IL-6)/signal transducer and activator of transcription 3 (STAT3) pathway inhibition may overcome chemoresistance of metastatic pancreatic cancer (MPC). We sought to determine the safety and recommended dose of tocilizumab (TCZ), an IL-6 receptor monoclonal antibody, and biological correlates of tumor shrinkage in patients with gemcitabine (GEM)/nanoparticle albumin-bound paclitaxel (nab-PTX)-refractory MPC. This phase 1 study enrolled 10 patients with MPC who had progressed after GEM/nab-PTX. Patients initially received TCZ 8 mg/kg on Day 1 and nab-PTX 100 mg/m

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCancer-Associated FibroblastsPancreatic NeoplasmsAgedAlbuminsDeoxycytidineDrug Resistance, NeoplasmFemaleGemcitabineHumansInterleukin-6MaleMiddle AgedPaclitaxelSTAT3 Transcription Factor130-nm albumin-bound paclitaxelAlbuminsAntibodies, Monoclonal, HumanizedDeoxycytidineGemcitabineInterleukin-6PaclitaxelSTAT3 protein, humanSTAT3 Transcription Factortocilizumabcancer associated fibroblastchemotherapyinterleukin-6pancreatic cancerrechallenge

Identifiers

PMID37605479
PMCPMC10551603
OpenAlexW4386046856

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.