Evidence map›Paper›PMID 37291587›Full record

ArticleWorld journal of surgical oncology2023

Gastrointestinal perforation after bevacizumab: a multi-site, single-institution study with a focus on survival.

Michael H Storandt, Nguyen H Tran, Christopher J Ehret, Mina Hanna, Jacob Jochum, Michael R Moynagh, Aminah Jatoi

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 5 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

7 authors at 2 institutions in 1 country.

Michael H StorandtDepartment of Medicine, 200 First Street SW, Rochester, MN, 55905, USA.
Nguyen H TranDepartment of Oncology, 200 First Street SW, Rochester, MN, 55905, USA.
Christopher J EhretDepartment of Oncology, 200 First Street SW, Rochester, MN, 55905, USA.
Mina HannaDepartment of Oncology, Mayo Clinic, 404 W. Fountain Street, Albert Lea, MN, 56007, USA.
Jacob JochumDepartment of Oncology, 200 First Street SW, Rochester, MN, 55905, USA.
Michael R MoynaghDepartment of Radiology, 200 First Street SW, Rochester, MN, 55905, USA.
Aminah JatoiDepartment of Oncology, 200 First Street SW, Rochester, MN, 55905, USA. jatoi.aminah@mayo.edu.
Mayo Clinic · USMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBevacizumab-induced gastrointestinal perforation is a rare but potentially devastating adverse event that has generated limited data on overall survival. Yet, such survival data are critical in guiding management.

methodsThis multi-site, single-institution retrospective study focused on all cancer patients who had received bevacizumab and who had suffered a well-documented gastrointestinal perforation from January 1, 2004 through January 20, 2022.The main goal was to report survival outcomes; Kaplan Meier curves and Cox survival models were used for this purpose.

resultsEighty-nine patients are included in this report with a median age of 62 years (range 26-85). Colorectal cancer was the most common malignancy (n = 42). Thirty-nine patients underwent surgery for the perforation. Seventy-eight were deceased at the time of reporting with an overall median survival of all patients of 2.7 months (range 0-45 months), and 32 (36%) died within 30 days of perforation. In univariable survival analyses, no statistically significant associations were observed for age, gender, corticosteroid use, and time since last bevacizumab dose. However, surgically treated patients manifested a better survival (hazard ratio (HR) 0.49 (95% CI 0.31-0.78); p = 0.003). In multivariable analyses, surgery continued to be associated with improved survival (HR 0.47 (95% CI 0.29-0.74); p = 0.002), and corticosteroid use was associated with worse survival (HR 1.75 (95% CI 1.02-2.99); p = 0.04).

conclusionAlthough gastrointestinal perforation after bevacizumab should be managed on a case-by-case basis, these descriptive survival data can help inform patients, their families, and healthcare providers as challenging management decisions arise.

Indexed as

Colorectal NeoplasmsNeoplasmsAdrenal Cortex HormonesAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabHumansMiddle AgedRetrospective StudiesAdrenal Cortex HormonesAntibodies, Monoclonal, HumanizedBevacizumabBevacizumabPerforationSurvival

Identifiers

PMID37291587
PMCPMC10249159
OpenAlexW4379966203

What OpenQuestion holds

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LicenceCC BY
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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.