Evidence map›Paper›PMID 38037752›Full record

ReviewCancer medicine2023

Novel immunotherapeutic options for BCG-unresponsive high-risk non-muscle-invasive bladder cancer.

Zein Alabdin Hannouneh, Amjad Hijazi, Alaa Aldeen Alsaleem, Siwan Hami, Nina Kheyrbek, Fadi Tanous, Karam Khaddour, Abdulfattah Abbas, Zuheir Alshehabi

Open access · goldAbstract readReview
In one paragraph

Review in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 31 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

9 authors at 3 institutions in 2 countries.

Zein Alabdin HannounehFaculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.ORCID 0000-0002-4516-9526
Amjad HijaziFaculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.ORCID 0009-0007-7054-6155
Alaa Aldeen AlsaleemFaculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.ORCID 0009-0001-6585-0255
Siwan HamiFaculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.ORCID 0009-0002-1220-7722
Nina KheyrbekCancer Research Center, Tishreen University, Lattakia, Syrian Arab Republic.ORCID 0000-0002-3435-6385
Fadi TanousCancer Research Center, Tishreen University, Lattakia, Syrian Arab Republic.ORCID 0009-0002-2749-7363
Karam KhaddourDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0001-6697-3516
Abdulfattah AbbasProfessor of Nephrology, Faculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.
Zuheir AlshehabiCancer Research Center, Tishreen University, Lattakia, Syrian Arab Republic.ORCID 0000-0002-6519-7954
Latakia University · SYAl Andalus University · SYHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-risk non-muscle-invasive bladder cancer (HR-NMIBC) presents a challenge to many physicians due to its ability to resist Bacillus Calmette-Guérin (BCG) intravesical therapy and the substantial rate of progression into muscle-invasive bladder cancer (MIBC). Patients who are BCG-unresponsive have worse prognosis and thus require further management including radical cystectomy (RC), which significantly impacts quality of life. Moreover, the ongoing worldwide shortage of BCG warrants the need for policies that prioritize drug use and utilize alternative treatment strategies. Hence, there is a significant unmet need for bladder preserving therapy in this subset of patients.

methodsTo address this issue, we searched the relevant literature in PUBMED for articles published from 2019 through May of 2023 using appropriate keywords. All clinical trials of patients with HR-NMIBC treated with immune-related agents were retrieved from clinicaltrials.gov. FINDINGS AND FUTURE PERSPECTIVES: Exploratory treatments for BCG-Unresponsive HR-NMIBC included immune checkpoint inhibitors (ICI), oncolytic viral therapy, cytokine agonists, and other immunomodulators targeting TLR, EpCaM, FGFR, MetAP2, and IDO1. Some combination therapies have been found to work synergistically and are preferred therapeutically over monotherapy. Three drugs-pembrolizumab, valrubicin, and most recently, nadofaragene firadenovec-vncg-have been FDA approved for the treatment of BCG-unresponsive NMIBC in patients who are ineligible for or decline RC. However, all explored treatment options tend to postpone RC rather than provide long-term disease control. Additional combination strategies need to be studied to enhance the effects of immunotherapy. Despite the challenges faced in finding effective therapies, many potential treatments are currently under investigation. Addressing the landscape of biomarkers, mechanisms of progression, BCG resistance, and trial design challenges in HR-NMIBC is essential for the discovery of new targets and the development of effective treatments.

Indexed as

Non-Muscle Invasive Bladder NeoplasmsUrinary Bladder NeoplasmsBCG VaccineHumansImmunotherapyNeoplasm InvasivenessNeoplasm Recurrence, LocalQuality of LifeBCG VaccineBacillus Calmette-Guérin-unresponsivegene therapyimmune checkpoint inhibitorsimmunotherapynon-muscle-invasive bladder canceroncolytic viral therapytargeted therapy

Identifiers

PMID38037752
PMCPMC10757155
OpenAlexW4389238191

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.