Evidence map›Paper›PMID 35949896›Full record

ArticleMolecular and clinical oncology2022

Short bevacizumab infusion as an effective and safe treatment for colorectal cancer.

Koichi Taira, Shunsuke Okazaki, Kohei Akiyoshi, Hirohisa Machida, Tetsuro Ikeya, Akie Kimura, Akinobu Nakata, Yuji Nadatani, Masaki Ohminami, Shusei Fukunaga and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Molecular and clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

16 authors at 4 institutions in 1 country.

Koichi TairaDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Shunsuke OkazakiDepartment of Clinical Oncology, Osaka City General Hospital, Osaka 534-0021, Japan.
Kohei AkiyoshiDepartment of Clinical Oncology, Osaka City General Hospital, Osaka 534-0021, Japan.
Hirohisa MachidaDepartment of Gastroenterology, Machida Gastrointestinal Hospital, Osaka 557-0001, Japan.
Tetsuro IkeyaDepartment of Surgery, Osaka Ekisaikai Hospital, Osaka 550-0022, Japan.
Akie KimuraDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Akinobu NakataDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Yuji NadataniDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Masaki OhminamiDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Shusei FukunagaDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Koji OtaniDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Shuhei HosomiDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Fumio TanakaDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Noriko KamataDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Yasuaki NagamiDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Yasuhiro FujiwaraDepartment of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Osaka Metropolitan UniversityTokyo Metropolitan University · JPOsaka City General Hospital · JPOsaka Ekisaikai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bevacizumab is a humanized monoclonal antibody that contains <10% murine protein. To prevent infusion-related hypersensitivity reactions (HSRs), the initial bevacizumab infusion is delivered for 90 min, the second for 60 min and subsequent doses for 30 min. Several previous studies have shown that short bevacizumab infusions are safe and do not result in severe HSRs in patients with colorectal, lung, ovarian and brain cancer. However, the efficacy of short bevacizumab infusions for colorectal cancer management remains unclear. Therefore, to investigate this issue, a prospective multicenter study was conducted using 23 patients enrolled between June 2017 and March 2019. The initial infusion of bevacizumab was for 30 min followed by a second infusion rate of 0.5 mg/kg/min (5 mg/kg over 10 min and 7.5 mg/kg over 15 min. The primary endpoint was progression-free survival (PFS). The overall response and disease control rates were 57 and 87%, respectively. The median PFS time was 306 days (interquartile range, 204-743 days). No HSRs were noted. Adverse events associated with bevacizumab included grade 4 small intestinal perforation and grade 3 stroke in 1 patient each. These results suggest that a short bevacizumab infusion regime comprising an initial infusion for 30 min followed by a second infusion at 0.5 mg/kg/min is safe and efficacious for the management of colorectal cancer.

Indexed as

bevacizumabcolorectal cancerinfusionPFStarget therapy

Identifiers

PMID35949896
PMCPMC9353868
OpenAlexW4288068268

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.