Evidence map›Paper›PMID 32935617›Full record

ArticleThe Journal of urology2021

Sequencing of PD-1/L1 Inhibitors and Carboplatin Based Chemotherapy for Cisplatin Ineligible Metastatic Urothelial Carcinoma.

Xiao X Wei, Lillian Werner, Min Y Teo, Jonathan E Rosenberg, Vadim S Koshkin, Petros Grivas, Bernadett Szabados, Laura Morrison, Thomas Powles, Lucia Carril-Ajuria and 12 more

Open access · greenAbstract readHistorical ArticleMulticenter Study
In one paragraph

Article in The Journal of urology, 2021. 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
0.6field-weighted citation impact, top 30% 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, 3 citations in OpenAlex.

  1. Article
  2. Article
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

22 authors at 13 institutions in 6 countries.

Xiao X WeiDana-Farber Cancer Institute, Boston, Massachusetts.
Lillian WernerDana-Farber Cancer Institute, Boston, Massachusetts.
Min Y TeoMemorial Sloan Kettering Cancer Center, New York, New York.
Jonathan E RosenbergMemorial Sloan Kettering Cancer Center, New York, New York.
Vadim S KoshkinUniversity of California San Francisco, San Francisco, California.
Petros GrivasUniversity of Washington School of Medicine and Fred Hutchinson Cancer Research Center, Seattle, Washington.
Bernadett SzabadosBarts Cancer Centre, Queen Mary University of London, London, United Kingdom.
Laura MorrisonBarts Cancer Centre, Queen Mary University of London, London, United Kingdom.
Thomas PowlesBarts Cancer Centre, Queen Mary University of London, London, United Kingdom.
Lucia Carril-AjuriaUniversitario de Octubre, Madrid, Spain.
Daniel CastellanoUniversitario de Octubre, Madrid, Spain.
Pedro Isaacsson VelhoSidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland.
Noah M HahnSidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland.
Rana R McKayUniversity of California San Diego, La Jolla, California.
Daniele RaggiFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Andrea NecchiFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Ravindran KanesvaranNational Cancer Centre Singapore, Singapore, Singapore.
Parissa AlerasoolTisch Cancer Institute at Mount Sinai, New York, New York.
Jacob GainesTisch Cancer Institute at Mount Sinai, New York, New York.
Matthew GalskyTisch Cancer Institute at Mount Sinai, New York, New York.
Joaquim BellmuntDana-Farber Cancer Institute, Boston, Massachusetts.
Guru SonpavdeDana-Farber Cancer Institute, Boston, Massachusetts.
Dana-Farber Cancer Institute · USQueen Mary University of London · GBFondazione IRCCS Istituto Nazionale dei Tumori · ITHospital Universitario 12 De Octubre · ESMemorial Sloan Kettering Cancer Center · USTisch Cancer InstituteHospital Moinhos de Vento · BRNational Cancer Centre Singapore · SGSidney Kimmel Comprehensive Cancer Center · USTisch Hospital · USUniversity of California, San Diego · USUniversity of California, San Francisco · USUniversity of Washington · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeCurrent first line treatment options in patients with metastatic urothelial carcinoma unfit to receive cisplatin containing chemotherapy include PD-1/L1 inhibitors and carboplatin containing chemotherapy. However, the optimal sequencing of these therapies remains unclear. MATERIALS AND

methodsWe conducted a multicenter retrospective analysis. Consecutive cisplatin ineligible patients with metastatic urothelial carcinoma treated with first line carboplatin containing chemotherapy followed sequentially by second line PD-1/L1 inhibitor, or the reverse order, were included. Patient demographics, objective response, time to treatment failure for first line and second line therapy, interval between end of first line and initiation of second line treatment (Interval

resultsIn this multicenter retrospective study we identified 146 cisplatin ineligible patients with metastatic urothelial carcinoma treated with first line PD-1/L1 inhibitor therapy followed by second line carboplatin containing chemotherapy (group 1, 43) or the reverse sequence (group 2, 103). In the overall cohort median age was 72, 76% were men and 18% had liver metastasis. In both groups objective response rates were higher with carboplatin containing chemotherapy (45.6% first line, 44.2% second line) compared to PD-1/L1 inhibitors (9.3% first line, 21.3% second line). On multivariate analysis treatment sequence was not associated with overall survival (HR 1.05, p=0.85). Site of metastasis was the only factor significantly associated with overall survival (p=0.002).

conclusionsIn this biomarker unselected cohort of cisplatin ineligible patients with metastatic urothelial carcinoma, PD-1/L1 inhibitor followed by carboplatin containing chemotherapy and the reverse sequence had comparable overall survival.

Indexed as

Antineoplastic AgentsCarboplatinCarcinoma, Transitional CellDrug Therapy, CombinationFemaleHistory, 18th CenturyHumansImmune Checkpoint InhibitorsMaleRetrospective StudiesUrinary Bladder NeoplasmsAntineoplastic AgentsCarboplatinImmune Checkpoint Inhibitorscarboplatincarcinomaprogrammed cell death 1 receptortransitional cellurinary bladder neoplasms

Identifiers

PMID32935617
PMCPMC8715311
OpenAlexW3087500946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.