Evidence map›Paper›PMID 33219618›Full record

ArticleThe oncologist2021

Comprehensive Genomic Profiling of Carcinoma of Unknown Primary Origin: Retrospective Molecular Classification Considering the CUPISCO Study Design.

Jeffrey S Ross, Ethan S Sokol, Holger Moch, Linda Mileshkin, Giulia Baciarello, Ferran Losa, Andreas Beringer, Marlene Thomas, Julia A Elvin, Nhu Ngo and 2 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03498521 (A Phase II, Randomized, Active-Controlled, Multi-Center Study Comparing the Efficacy and Safety of Targeted Therapy or Cancer Immunotherapy Guided by Genomic Profiling Versus Platinum-Based Chemotherapy in Patients With Cancer of Unknown Primary Site Who Have Received Three Cycles of Platinum Doublet Chemotherapy), which is not on this map. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
3.3field-weighted citation impact, top 6% 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.

NCT03498521 phase2completednot on this map

A Phase II, Randomized, Active-Controlled, Multi-Center Study Comparing the Efficacy and Safety of Targeted Therapy or Cancer Immunotherapy Guided by Genomic Profiling Versus Platinum-Based Chemotherapy in Patients With Cancer of Unknown Primary Site Who Have Received Three Cycles of Platinum Doublet Chemotherapy

TypeinterventionalSponsorHoffmann-La RocheRan2018 to 2024Enrolled529ConditionsCancer of Unknown Primary SiteArmsAlectinib, Vismodegib, Ipatasertib, Olaparib, Erlotinib
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 3 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. SEOM-GECOD clinical guideline for cancer of unknown primary (update 2025).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Guideline
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  3. SEOM-GECOD clinical guideline for unknown primary cancer (2021).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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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

12 authors at 7 institutions in 6 countries.

Jeffrey S RossFoundation Medicine, Inc., Cambridge, Massachusetts, USA.ORCID 0000-0001-8494-2596
Ethan S SokolFoundation Medicine, Inc., Cambridge, Massachusetts, USA.ORCID 0000-0002-2988-0537
Holger MochUniversity of Zurich and University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-7986-2839
Linda MileshkinPeter MacCallum Cancer Centre, Melbourne, Victoria, Australia.ORCID 0000-0001-6826-6014
Giulia BaciarelloGustave Roussy, Villejuif, France.ORCID 0000-0002-5396-5071
Ferran LosaHospital de Sant Joan Despí Moisès Broggi, Barcelona, Spain.ORCID 0000-0003-4355-6626
Andreas BeringerF. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0002-3893-8606
Marlene ThomasF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Julia A ElvinFoundation Medicine, Inc., Cambridge, Massachusetts, USA.ORCID 0000-0001-9476-9563
Nhu NgoFoundation Medicine, Inc., Cambridge, Massachusetts, USA.ORCID 0000-0001-5054-0281
Dexter X JinFoundation Medicine, Inc., Cambridge, Massachusetts, USA.ORCID 0000-0003-1533-6730
Alwin KrämerGerman Cancer Research Center (DKFZ) and University of Heidelberg, Heidelberg, Germany.
Foundation Medicine (United States)Roche (Switzerland) · CHHeidelberg University · DEHospital de Sant Joan Despí Moisès Broggi · ESInstitut Gustave Roussy · FRPeter MacCallum Cancer Centre · AUUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarcinoma of unknown primary origin (CUP) accounts for 2%-5% of newly diagnosed advanced malignancies, with chemotherapy as the standard of care. CUPISCO (NCT03498521) is an ongoing randomized trial using comprehensive genomic profiling (CGP) to assign patients with CUP to targeted or immunotherapy treatment arms based on genomic profiling. We performed a retrospective analysis of CUP cases referred for CGP to determine how many were potentially eligible for enrollment into an experimental CUPISCO arm. MATERIALS AND

methodsCentrally reviewed adenocarcinoma and undifferentiated CUP specimens in the FoundationCore database were analyzed using the hybrid capture-based FoundationOne CDx assay (mean coverage, >600×). Presence of genomic alterations, microsatellite instability (MSI), tumor mutational burden (TMB), genomic loss of heterozygosity (gLOH), and programmed death-ligand 1 (PD-L1) positivity were determined.

resultsA total of 96 of 303 patients (31.7%) could be matched to an experimental CUPISCO arm. Key genomic alterations included ERBB2 (7.3%), PIK3CA (6.3%), NF1 (5.6%), NF2 (4.6%), BRAF (4.3%), IDH1 (3.3%), PTEN, FGFR2, EGFR (3.6% each), MET (4.3%), CDK6 (3.0%), FBXW7, CDK4 (2.3% each), IDH2, RET, ROS1, NTRK (1.0% each), and ALK (0.7%). Median TMB was 3.75 mutations per megabase of DNA; 34 patients (11.6%) had a TMB ≥16 mutations per megabase. Three patients (1%) had high MSI, and 42 (14%) displayed high PD-L1 expression (tumor proportion score ≥50%). gLOH could be assessed in 199 of 303 specimens; 19.6% had a score of >16%.

conclusionsThirty-two percent of patients would have been eligible for targeted therapy in CUPISCO. Future studies, including additional biomarkers such as PD-L1 positivity and gLOH, may identify a greater proportion potentially benefiting from CGP-informed treatment. Clinical trial identification number. NCT03498521 IMPLICATIONS FOR PRACTICE: The findings of this retrospective analysis of carcinoma of unknown primary origin (CUP) cases validate the experimental treatment arms being used in the CUPISCO study (NCT03498521), an ongoing randomized trial using comprehensive genomic profiling to assign patients with CUP to targeted or immunotherapy treatment arms based on the presence of pathogenic genomic alterations. The findings also suggest that future studies including additional biomarkers and treatment arms, such as programmed death-ligand 1 positivity and genomic loss of heterozygosity, may identify a greater proportion of patients with CUP potentially benefiting from comprehensive genomic profiling-informed treatment.

Indexed as

CarcinomaLung NeoplasmsNeoplasms, Unknown PrimaryBiomarkers, TumorGene Expression ProfilingGenomicsHumansMutationProtein-Tyrosine KinasesProto-Oncogene ProteinsRetrospective StudiesBiomarkers, TumorProtein-Tyrosine KinasesProto-Oncogene ProteinsGenetic profilingLoss of heterozygosityMolecular targeted therapyUnknown primary tumors

Identifiers

PMID33219618
PMCPMC7930409
OpenAlexW3105588600

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Registered trials

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.