Evidence map›Paper›PMID 33774697›Full record

ArticleCancer immunology, immunotherapy : CII2021

Clinical outcome of patients with metastatic melanoma of unknown primary in the era of novel therapy.

Danielle Verver, Dirk J Grünhagen, Alexander C J van Akkooi, Maureen J B Aarts, Franchette W P J van den Berkmortel, Alfonsus J M van den Eertwegh, Jan Willem B de Groot, Marye J Boers-Sonderen, John B A G Haanen, Geke A P Hospers and 8 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. 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. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Melanoma of unknown primary presenting as intestinal obstruction: a diagnostic challenge.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

18 authors.

Danielle VerverDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Dr Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands. d.verver@erasmusmc.nl.ORCID http://orcid.org/0000-0003-0034-3575
Dirk J GrünhagenDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Dr Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Alexander C J van AkkooiDepartment of Surgical Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Maureen J B AartsDepartment of Medical Oncology, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Franchette W P J van den BerkmortelDepartment of Medical Oncology, Zuyderland Medical Centre, Sittard-Geleen, The Netherlands.
Alfonsus J M van den EertweghDepartment of Medical Oncology, Amsterdam UMC, Location VU University Medical Centre (VUmc), Cancer Centre Amsterdam, Amsterdam, The Netherlands.
Jan Willem B de GrootOncology Centre Isala, Isala, Zwolle, The Netherlands.
Marye J Boers-SonderenDepartment of Medical Oncology, Radboud University Medical Centre, Nijmegen, The Netherlands.
John B A G HaanenDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Geke A P HospersDepartment of Medical Oncology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Ellen KapiteijnDepartment of Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
Djura PiersmaDepartment of Internal Medicine, Medisch Spectrum Twente, Enschede, The Netherlands.
Rozemarijn S van RijnDepartment of Internal Medicine, Medical Centre Leeuwarden, Leeuwarden, The Netherlands.
Karijn P M SuijkerbuijkDepartment of Medical Oncology, University Medical Centre Utrecht Cancer Centre, Utrecht, The Netherlands.
Albert J Ten TijeDepartment of Internal Medicine, Amphia Hospital, Breda, The Netherlands.
Gerard VreugdenhilDepartment of Internal Medicine, Maxima Medical Centre, Eindhoven, The Netherlands.
Cornelis VerhoefDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Dr Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Astrid A M van der VeldtDepartments of Medical Oncology and Radiology and Nuclear Medicine, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Funding

ZonMw 836002002
6 · The paper itself

Abstract

Melanoma of unknown primary (MUP) is considered different from melanoma of known primary (MKP), and it is unclear whether these patients benefit equally from novel therapies. In the current study, characteristics and overall survival (OS) of patients with advanced and metastatic MUP and MKP were compared in the era of novel therapy. Patients were selected from the prospective nation-wide Dutch Melanoma Treatment Registry (DMTR). The following criteria were applied: diagnosis of stage IIIc unresectable or IV cutaneous MKP (cMKP) or MUP between July 2012 and July 2017 and treatment with immune checkpoint inhibition and/or targeted therapy. OS was estimated using the Kaplan-Meier method. The stratified multivariable Cox regression model was used for adjusted analysis. A total of 2706 patients were eligible including 2321 (85.8%) patients with cMKP and 385 (14.2%) with MUP. In comparative analysis, MUP patients more often presented with advanced and metastatic disease at primary diagnosis with poorer performance status, higher LDH, and central nervous system metastases. In crude analysis, median OS of cMKP or MUP patients was 12 months (interquartile range [IQR] 5 - 44) and 14 months (IQR 5 - not reached), respectively (P = 0.278). In adjusted analysis, OS in MUP patients was superior (hazard rate 0.70, 95% confidence interval 0.58-0.85; P < 0.001). As compared to patients with advanced and metastatic cMKP, MUP patients have superior survival in adjusted analysis, but usually present with poorer prognostic characteristics. In crude analysis, OS was comparable indicating that patients with MUP benefit at least equally from treatment with novel therapies.

Indexed as

AgedAntineoplastic AgentsFemaleHumansImmune Checkpoint InhibitorsMaleMelanomaMiddle AgedMolecular Targeted TherapyNeoplasms, Unknown PrimarySkin NeoplasmsAntineoplastic AgentsImmune Checkpoint InhibitorsKnown primaryMelanomaNovel therapyUnknown primary

Identifiers

PMID33774697
PMCPMC8505371

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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.