Evidence map›Paper›PMID 35305098›Full record

ArticleThe oncologist2022

Evaluation of Targeted Next-Generation Sequencing for the Management of Patients Diagnosed with a Cancer of Unknown Primary.

Michael J Fusco, Todd C Knepper, Juliana Balliu, Alex Del Cueto, Jose M Laborde, Sharjeel M Hooda, Andrew S Brohl, Marilyn M Bui, J Kevin Hicks

Abstract read
In one paragraph

Article in The oncologist, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. When neck lymph nodes metastases do not origin from a head and neck unknown primary.Current opinion in otolaryngology & head and neck surgery · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. 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

9 authors.

Michael J FuscoDepartment of Individualized Cancer Management, Section for Precision Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.ORCID 0000-0002-5883-7466
Todd C KnepperDepartment of Individualized Cancer Management, Section for Precision Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Juliana BalliuDepartment of Individualized Cancer Management, Section for Precision Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Alex Del CuetoDepartment of Individualized Cancer Management, Section for Precision Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Jose M LabordeDepartment of Biostatistics and Bioinformatics, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Sharjeel M HoodaDepartment of Satellite and Community Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Andrew S BrohlSarcoma Department, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
Marilyn M BuiDepartment of Pathology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.
J Kevin HicksDepartment of Individualized Cancer Management, Section for Precision Oncology, Moffitt Comprehensive Cancer Center, Tampa, FL, USA.

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Moffitt Cancer Center P30-CA076292NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

backgroundCancer of unknown primary (CUP) comprises a heterogeneous collection of malignancies that are typically associated with a poor prognosis and a lack of effective treatment options. We retrospectively evaluated the clinical utility of targeted next-generation sequencing (NGS) among CUP patients to assist with diagnosis and identify opportunities for molecularly guided therapy. PATIENTS AND

methodsPatients with a CUP at Moffitt Cancer Center who underwent NGS between January 1, 2014 and December 31, 2019, were eligible for study inclusion. Next-generation sequencing results were assessed to determine the frequency of clinically actionable molecular alterations, and chart reviews were performed to ascertain the number of patients receiving molecularly guided therapy.

resultsNinety-five CUP patients were identified for analysis. Next-generation sequencing testing identified options for molecularly guided therapy for 55% (n = 52) of patients. Among patients with molecularly guided therapy options, 33% (n = 17) were prescribed a molecularly guided therapy. The median overall survival for those receiving molecularly guided therapy was 23.6 months. Among the evaluable patients, the median duration of treatment for CUP patients (n = 7) receiving molecular-guided therapy as a first-line therapy was 39 weeks. The median duration of treatment for CUP patients (n = 8) treated with molecularly guided therapy in the second- or later-line setting was 13 weeks. Next-generation sequencing results were found to be suggestive of a likely primary tumor type for 15% (n = 14) of patients.

conclusionNext-generation sequencing results enabled the identification of treatment options in a majority of patients and assisted with the identification of a likely primary tumor type in a clinically meaningful subset of patients.

Indexed as

Neoplasms, Unknown PrimaryHigh-Throughput Nucleotide SequencingHumansRetrospective StudiesTreatment Outcomecancer geneticscancer of unknown primarynext generation sequencingpharmacogeneticsprecision medicine

Identifiers

PMID35305098
PMCPMC8842368

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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.