Evidence map›Paper›PMID 29478343›Full record

ReviewExpert review of clinical pharmacology2018

PD-L1 inhibition with avelumab for metastatic Merkel cell carcinoma.

Maria Rita Gaiser, Michelle Bongiorno, Isaac Brownell

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Expert review of clinical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02155647 (A Phase II, Open-Label, Multicenter Trial to Investigate the Clinical Activity and Safety of Avelumab), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 13% 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.

NCT02155647 phase2completednot on this map

A Phase II, Open-Label, Multicenter Trial to Investigate the Clinical Activity and Safety of Avelumab (MSB0010718C) in Subjects With Merkel Cell Carcinoma

TypeinterventionalSponsorEMD Serono Research & Development Institute, Inc.Ran2014 to 2023Enrolled204ConditionsCarcinoma, Merkel CellArmsAvelumab
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Immune Checkpoint Inhibitors in Cancer Therapy.Current oncology (Toronto, Ont.) · 2022
    Review
  11. Review
  12. [Local tumor control of metastatic Merkel cell carcinoma in a 90-year-old woman].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 3 institutions in 2 countries.

Maria Rita Gaisera Skin Cancer Unit , German Cancer Research Center (DKFZ) , Heidelberg , Germany.
Michelle Bongiornoc Naval Health Clinic Hawaii , Pearl Harbor , HI , USA.
Isaac Brownelld Dermatology Branch , Center for Cancer Research, National Cancer Institute, National Institutes of Health , Bethesda , MD , USA.
Bay Clinic · USNational Cancer Institute · USUniversity Hospital Heidelberg · DE

Funding

Development and regulation of stem cell lineages in skinZIABC011393 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BROWNELL, ISAAC · 2011 to 2021
$6.7M
Ipilimumab for treatment of advanced Merkel cell carcinomaZIABC011450 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BROWNELL, ISAAC · 2012 to 2021
$1.0M
Intramural NIH HHS ZIA BC011450
6 · The paper itself

Abstract

introductionMerkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine skin cancer that lacks durable responses to traditional chemotherapy. Areas covered: After MCC was shown to be an immunogenic tumor, small trials revealed high objective response rates to PD-1/PD-L1 checkpoint inhibitors. The JAVELIN Merkel 200 (NCT02155647) trial tested the use of avelumab, a human IgG1 monoclonal antibody against PD-L1, in metastatic MCC. Avelumab recently became the first approved drug for metastatic MCC. Expert commentary: By conducting broad phase I studies assessing the safety of avelumab and a small phase II study demonstrating efficacy in this rare orphan tumor type, avelumab gained accelerated approval for the treatment of metastatic MCC. Additional studies are needed to determine how the antibody-dependent cellular cytotoxicity (ADCC) competent Fc region of avelumab contributes to disease control. Remaining questions: Longer follow-up will determine the durability of checkpoint blockade in controlling metastatic MCC. Additional studies will assess the utility and safety of adjuvant checkpoint blockade in patients with excised MCC. How to increase response rates by combining PD-1/PD-L1 blockade with other treatment approaches needs to be explored. In addition, treatment options for MCC patients who fail or do not respond to avelumab need to be identified.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsB7-H1 AntigenCarcinoma, Merkel CellHumansMiceNeoplasm MetastasisSkin NeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsavelumabB7-H1 AntigenCD274 protein, humanAnti-PD-1anti-PD-L1avelumabBavenciocheckpoint inhibitorimmunotherapyMerkel cell carcinomapembrolizumab

Identifiers

PMID29478343
PMCPMC6360093
OpenAlexW2791527593

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.