Evidence map›Paper›PMID 39061200›Full record

ArticleCancers2024

Sequential Endoluminal Gemcitabine and Cabazitaxel with Intravenous Pembrolizumab as a Bladder-Preserving Strategy for Docetaxel-Unresponsive Non-Muscle Invasive Urothelial Carcinoma Following Transurethral Resection of Bladder Tumor.

Ian M McElree, Vignesh T Packiam, Ryan L Steinberg, Helen Y Hougen, Sarah L Mott, Mohamad Abou Chakra, Yousef Zakharia, Michael A O'Donnell

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

8 authors.

Ian M McElreeCarver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-9991-4301
Vignesh T PackiamRutgers Cancer Institute of New Jersey, Division of Urology, Department of Surgery, New Brunswick, NJ 08903, USA.ORCID 0000-0001-8397-7797
Ryan L SteinbergDepartment of Urology, University of Iowa, Iowa City, IA 52242, USA.
Helen Y HougenDepartment of Urology, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-3141-6474
Sarah L MottHolden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52242, USA.
Mohamad Abou ChakraDepartment of Urology, University of Iowa, Iowa City, IA 52242, USA.
Yousef ZakhariaHolden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-9480-2626
Michael A O'DonnellDepartment of Urology, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-7202-6427

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Mark E Burkard · 2000 to 2026
$70.0M
NCI NIH HHS P30 CA086862The John & Carol Walter Family Foundation N/A
6 · The paper itself

Abstract

Growing evidence suggests that many patients with high-risk non-muscle invasive urothelial carcinoma (NMIUC) can undergo bladder-sparing management with salvage intravesical therapies. However, inherent or developed disease resistance, particularly after multiple lines of prior salvage therapy, implores the continued pursuit of new treatment combinations. Herein, we describe the outcomes of 26 patients (31 treated units; 24 lower tract, 7 upper tract) with high-risk NMIUC treated with sequential intravesical gemcitabine and cabazitaxel with concomitant intravenous pembrolizumab (GCP) at the University of Iowa from August 2020 to February 2023. Median (IQR) follow-up was 30 (IQR: 17-35) months. Treated units had a history of high-risk NMIUC with a median of four prior endoluminal inductions. Overall, 87% of units presented with CIS or positive urine cytology. The 1- and 2-year recurrence-free survival was 77% (CI: 58-88%) and 52% (CI: 30-70%), respectively. The 2-year progression-free and cancer-specific survival was 70% (CI: 44-85%) and 96% (CI: 75-99%), respectively. In total, 22/26 (85%) patients reported any adverse event and 5/26 (19%) reported a grade ≥3 adverse event; however, all patients tolerated a full induction course. These results suggest that GCP is an effective and tolerable treatment option for patients with recurrent high-risk NMIUC.

Indexed as

cabazitaxelgemcitabinepembrolizumaburinary bladder neoplasms

Identifiers

PMID39061200
PMCPMC11274621

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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.