Evidence map›Paper›PMID 39797702›Full record

Trial reportFuture oncology (London, England)2025

CASE (CemiplimAb-rwlc Survivorship and Epidemiology): a study in advanced basal cell carcinoma.

Soo J Park, David M Ellison, Ryan Weight, Jade Homsi, Guilherme Rabinowits, Emily S Ruiz, John Strasswimmer, Josh Simmons, Timothy Panella, Ruben Gw Quek and 2 more

Registry-linked trialAbstract readClinical Trial, Phase IVMulticenter Study
In one paragraph

Trial report in Future oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03836105 (Cemiplimab Survivorship Epidemiology), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT03836105 completednot on this map

Cemiplimab Survivorship Epidemiology (CASE) Study

TypeobservationalSponsorRegeneron PharmaceuticalsRan2019 to 2025Enrolled287ConditionsCutaneous Squamous Cell Carcinoma, Basal Cell CarcinomaArmscemiplimab
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Soo J ParkDepartment of Medicine, Division of Hematology and Oncology, University of California San Diego, La Jolla, CA, USA.
David M EllisonCharleston Oncology, Charleston, SC, USA.
Ryan WeightThe Melanoma and Skin Cancer Institute, Denver, CO, USA.
Jade HomsiDivision of Hematology and Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Guilherme RabinowitsDepartment of Hematology and Oncology, Miami Cancer Institute/Baptist Health South Florida, Miami, FL, USA.
Emily S RuizDepartment of Dermatology, Brigham and Women's Hospital, Boston, MA, USA.
John StrasswimmerCollege of Medicine (Dermatology) and College of Sciences (Biochemistry), Florida Atlantic University, Boca Raton, FL, USA.
Josh SimmonsDepartment of Hematology/Medical Oncology, Archbold Cancer Center, Thomasville, GA, USA.
Timothy PanellaDivision of Hematology and Oncology, University of Tennessee Medical Center, Knoxville, TN, USA.
Ruben Gw QuekRegeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
Jean-Francois PouliotRegeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
Nikhil I KhushalaniDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients diagnosed with metastatic basal cell carcinoma (BCC) have a poor prognosis. The current standard of care for adults with locally advanced or metastatic BCC who are not candidates for surgery or radiation therapy is treatment with hedgehog pathway inhibitors (HHIs). For patients who progress while on this therapy, further treatment options are limited. There is also a need for real-world clinical practice data on the clinical characteristics, management, disease progression, and survivorship of these patients. The ongoing CemiplimAb-rwlc Survivorship and Epidemiology (CASE) study is a phase IV, multicenter, prospective, noninterventional survivorship and epidemiology cohort study evaluating the effectiveness and safety of cemiplimab, a fully human immunoglobulin G4 monoclonal antibody that blocks the interaction between the programmed cell death-1 (PD-1) receptor and its ligands. This paper describes one cohort of the CASE study of patients with locally advanced or metastatic BCC who have failed or are intolerant of HHIs or for whom HHI therapy is not appropriate. Outcome measures of the study include response to treatment, quality of life, safety, treatment patterns, patient experience, and survival. This study could provide a more complete characterization of this patient population and fill knowledge gaps related to real-world treatment utilization and patient outcomes.Clinical Trial registration: NCT03836105.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBasal Cell CarcinomaSkin NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesQuality of LifeTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalcemiplimabBasal cell carcinomacemiplimabclinical trialepidemiologyPD-1 inhibitorprotocolsurvivorship

Identifiers

PMID39797702
PMCPMC11812358

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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.