Evidence map›Paper›PMID 35617646›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2022

Longitudinal Molecular Profiling of Circulating Tumor Cells in Metastatic Renal Cell Carcinoma.

Matthew Bootsma, Rana R McKay, Hamid Emamekhoo, Rory M Bade, Jennifer L Schehr, Matthew C Mannino, Anupama Singh, Serena K Wolfe, Zachery D Schultz, Jamie Sperger and 19 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  7. Turning the tide: pembrolizumab's triumph in adjuvant RCC therapy.Medical oncology (Northwood, London, England) · 2024
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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

29 authors at 4 institutions in 1 country.

Matthew BootsmaDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0003-0879-5066
Rana R McKayMoores Cancer Center, University of California San Diego, La Jolla, CA.ORCID 0000-0002-0581-7963
Hamid EmamekhooDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-8506-8703
Rory M BadeDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Jennifer L SchehrDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Matthew C ManninoDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Anupama SinghDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Serena K WolfeDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Zachery D SchultzDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Jamie SpergerDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0001-8578-8033
Wanling XieDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-5995-8000
Sabina SignorettiDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-5000-9105
Christos E KyriakopoulosDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-6452-7405
David KosoffDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.
Edwin J AbelUrology, University of Wisconsin-Madison, Madison, WI.
Kyle T HelzerDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0003-3853-5564
Nicholas RydzewskiDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.
Hamza BakhtiarDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0001-7412-5525
Yue ShiDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-2860-2666
Grace BlitzerDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0003-3178-3004
Michael BassettiDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.
John FlobergDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-7635-7554
Menggang YuDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-7904-3155
Nan SethakornDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-7395-3182
Marina SharifiDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0003-0128-3033
Paul M HarariDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.
Toni K ChoueiriDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-9201-3217
Joshua M LangDepartment of Medicine, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-0943-8872
Shuang G ZhaoDepartment of Human Oncology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-9166-6507
University of Wisconsin–Madison · USDana-Farber Cancer Institute · USBrigham and Women's Hospital · USUniversity of California San Diego · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
DYNAMIC MOLECULAR EVOLUTION OF TREATMENT RESISTANT CANCERDP2CA271832 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI ZHAO, SHUANG · 2021 to 2024
$2.3M
NCI NIH HHS DP2 CA271832NCI NIH HHS P30 CA014520
6 · The paper itself

Abstract

purposeLiquid biopsies in metastatic renal cell carcinoma (mRCC) provide a unique approach to understand the molecular basis of treatment response and resistance. This is particularly important in the context of immunotherapies, which target key immune-tumor interactions. Unlike metastatic tissue biopsies, serial real-time profiling of mRCC is feasible with our noninvasive circulating tumor cell (CTC) approach.

methodsWe collected 457 longitudinal liquid biopsies from 104 patients with mRCC enrolled in one of two studies, either a prospective cohort or a phase II multicenter adaptive immunotherapy trial. Using a novel CTC capture and automated microscopy platform, we profiled CTC enumeration and expression of HLA I and programmed cell death-ligand 1 (PD-L1). Given their diametric immunological roles, we focused on the HLA I to PD-L1 ratio (HP ratio).

resultsPatients with radiographic responses showed significantly lower CTC abundances throughout treatment. Furthermore, patients whose CTC enumeration trajectory was in the highest quartile (> 0.12 CTCs/mL annually) had shorter overall survival (median 17.0 months

conclusionIn the first large longitudinal CTC study in mRCC to date to our knowledge, we identified the prognostic importance of CTC enumeration and the change over time of both CTC enumeration and the HP ratio. These insights into changes in both tumor burden and the molecular profile of tumor cells in response to different treatments provide potential biomarkers to predict and monitor response to immunotherapy in mRCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsNeoplastic Cells, CirculatingB7-H1 AntigenBiomarkers, TumorHumansPrognosisProspective StudiesB7-H1 AntigenBiomarkers, Tumor

Identifiers

PMID35617646
PMCPMC9622626
OpenAlexW4281550254

What OpenQuestion holds

Textmetadata
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.