Evidence map›Paper›PMID 30420974›Full record

ArticleEuropean urology oncology2018

Neoadjuvant Dose-dense Gemcitabine and Cisplatin in Muscle-invasive Bladder Cancer: Results of a Phase 2 Trial.

Fern Anari, John O'Neill, Woonyoung Choi, David Y T Chen, Mohammed Haseebuddin, Alexander Kutikov, Essel Dulaimi, R Katherine Alpaugh, Karthik Devarajan, Richard E Greenberg and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in European urology oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  14. Update on bladder cancer molecular subtypes.Translational andrology and urology · 2020
    Review
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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

24 authors at 4 institutions in 1 country.

Fern AnariFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
John O'NeillFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Woonyoung ChoiJohns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.
David Y T ChenFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Mohammed HaseebuddinFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Alexander KutikovFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Essel DulaimiFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
R Katherine AlpaughFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Karthik DevarajanFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Richard E GreenbergFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Marijo BilusicFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Yu-Ning WongFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Rosalia ViterboFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Jean H Hoffman-CensitsSidney Kimmel Cancer Center at Jefferson, Philadelphia, PA, USA.
Costas D LallasSidney Kimmel Cancer Center at Jefferson, Philadelphia, PA, USA.
Edouard J TrabulsiSidney Kimmel Cancer Center at Jefferson, Philadelphia, PA, USA.
Marc SmaldoneFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Daniel M GeynismanFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Matthew ZibelmanFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Jianqing LinSidney Kimmel Cancer Center at Jefferson, Philadelphia, PA, USA.
W Kevin KellySidney Kimmel Cancer Center at Jefferson, Philadelphia, PA, USA.
Robert UzzoFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
David McConkeyJohns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.
Elizabeth R PlimackFox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Temple University Health System · USFox Chase Cancer Center · USSidney Kimmel Cancer Center · USBladder Cancer Advocacy Network · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHARNITA M. ZEIGLER-JOHNSON · 1985 to 2026
$138.8M
NIH Hematology Oncology Fellowship ProgramZIEBC010843 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HILL, ELIZABETH · 2009 to 2025
$104.7M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

backgroundAccelerated (also termed dose-dense, DD) chemotherapy regimens such as accelerated methotrexate, vinblastine, doxorubicin, and cisplatin have shown better efficacy and tolerability in the metastatic setting, and shortened the time to surgery in the neoadjuvant setting compared to standard-schedule regimens. We hypothesized that a DD schedule of gemcitabine and cisplatin (GC) would shorten the time to surgery and yield similar pathologic complete response rates (pT0) in patients with muscle-invasive bladder cancer (MIBC) compared with historical controls with standard GC.

objectiveTo determine the safety and efficacy of neoadjuvant DDGC in MIBC. DESIGN SETTING AND

participantsPatients with cT2-4a, N0-1, M0 MIBC were eligible and received three 14-d cycles of DDGC with pegfilgrastim support followed by radical cystectomy with lymph node dissection. The primary end point was the pT0 rate. Molecular subtypes were assigned and correlated with survival. RESULTS AND LIMITATIONS: Thirty-one patients were evaluable for toxicity and response, of whom 58% had baseline clinical stage >T2N0M0; the median age was 69 yr. Ten patients (32%, 95% confidence interval [CI] 16-49%) achieved ypT0N0 status at cystectomy. Another four patients (13%, 95% CI 1-25%) were downstaged to non-muscle-invasive (<pT2N0) disease. Most patients (54.8%) experienced only grade 1-2 treatment-related toxicities. However, seven patients (23%) had clinically significant vascular events, leading to early closure of the study. Thirty patients (94%) underwent cystectomy. The median time from the start of chemotherapy to cystectomy was 9.3 wk. There was no correlation between molecular subtypes and survival.

conclusionsDDGC yielded a similar pT0 rate to that noted retrospectively with standard GC. Vascular events precluded, delayed, or increased the risk of surgery for 23% of patients, resulting in early closure of the study. Additional prospective studies with embedded biomarker correlatives of GC in the neoadjuvant setting are critical to accurately define both the activity and toxicity of this combination in MIBC. PATIENT SUMMARY: Neoadjuvant chemotherapy before cystectomy is the standard of care for muscle-invasive bladder cancer (MIBC). This prospective phase 2 study tested a dose-dense schedule of gemcitabine and cisplatin in MIBC. The study was closed early because of a higher than expected rate of vascular events. These data suggest that caution is required in using this regimen, particularly when there is better prospective evidence for the safety and efficacy of alternative regimens such as dose-dense or accelerated methotrexate, vinblastine, doxorubicin, and cisplatin.

Identifiers

PMID30420974
PMCPMC6226048
OpenAlexW2807188318

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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.