Evidence map›Paper›PMID 32821373›Full record

ArticleMelanoma management2020

Observational study of talimogene laherparepvec use in the anti-PD-1 era for melanoma in the US (COSMUS-2).

James Sun, Brian R Gastman, Lucy McCahon, Elizabeth I Buchbinder, Igor Puzanov, Michele Nanni, James M Lewis, Richard D Carvajal, Shahnaz Singh-Kandah, Anupam M Desai and 4 more

Abstract read
In one paragraph

Article in Melanoma management, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Tuning epigenetics to enhance cancer virotherapy.Acta pharmaceutica Sinica. B · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Therapy with oncolytic viruses: progress and challenges.Nature reviews. Clinical oncology · 2023
    Review
  7. Intratumoral therapies and in-situ vaccination for melanoma.Human vaccines & immunotherapeutics · 2022
    Review
  8. 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

14 authors.

James SunDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL 33612, USA.ORCID https://orcid.org/0000-0002-9915-6974
Brian R GastmanDepartment of Plastic Surgery, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Lucy McCahonDepartment of Plastic Surgery, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Elizabeth I BuchbinderDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Igor PuzanovDepartment of Medical Oncology, Roswell Park Cancer Institute, Buffalo, NY 14203, USA.
Michele NanniDepartment of Medical Oncology, Roswell Park Cancer Institute, Buffalo, NY 14203, USA.
James M LewisDepartment of Surgical Oncology, University of Tennessee Graduate School of Medicine, Knoxville, TN 37920, USA.
Richard D CarvajalDepartment of Medical Oncology, Columbia University Irving Medical Center, New York, NY 37996, USA.
Shahnaz Singh-KandahDepartment of Medical Oncology, Columbia University Irving Medical Center, New York, NY 37996, USA.
Anupam M DesaiDepartment of Medical Oncology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Leon RaskinAmgen Inc., Thousand Oaks, CA 91320, USA.
Carrie M NielsonAmgen Inc., Thousand Oaks, CA 91320, USA.
Rubina IsmailAmgen Inc., Thousand Oaks, CA 91320, USA.
Jonathan S ZagerDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL 33612, USA.ORCID https://orcid.org/0000-0002-6886-4468

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTalimogene laherparepvec (T-VEC) is an intralesional therapy for unresectable, metastatic melanoma. T-VEC real-world use in the context of anti-PD1-based therapy requires further characterization. MATERIALS &

methodsA retrospective review of T-VEC use from 1 January 2017 and 31 March 2018 for melanoma patients was conducted at seven US institutions.

resultsAmong 83 patients, three categories of T-VEC and anti-PD-1 therapy were identified: T-VEC used without anti-PD-1 (n = 29, 35%), T-VEC after anti-PD-1-based therapy (n = 22, 27%) and concurrent T-VEC and anti-PD-1-based therapy (n = 32, 39%). 25% of patients discontinued T-VEC therapy due to no remaining injectable lesions, 37% discontinued T-VEC due to progressive disease. Discontinuation of T-VEC did not differ by anti-PD-1-based therapy use or timing.

conclusionIn real-world settings, T-VEC may be used concurrently with or after anti-PD-1-based therapy.

Indexed as

combination therapyimmunotherapymetastatic melanomaoncolytic virusreal-world evidencetalimogene laherparepvecT-VEC

Identifiers

PMID32821373
PMCPMC7426742

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.