Evidence map›Paper›PMID 31187176›Full record

ArticleCancer immunology, immunotherapy : CII2019

Combination of denosumab and immune checkpoint inhibition: experience in 29 patients with metastatic melanoma and bone metastases.

Yenny Angela, Sebastian Haferkamp, Carsten Weishaupt, Selma Ugurel, Jürgen C Becker, Florian Oberndörfer, Vesna Alar, Imke Satzger, Ralf Gutzmer

Abstract readMulticenter Study
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
–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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Response rate specific to bone metastasis of various cancers for immune checkpoint inhibitors: a systematic review.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2024
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  11. Denosumab Induces Neoplastic Stromal Cell ApoptosisCurrent cancer drug targets · 2024
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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

9 authors.

Yenny AngelaDepartment of Dermatology and Allergy, Skin Cancer Center Hannover, Medizinische Hochschule Hannover, Carl Neuberg Str. 1, 30625, Hannover, Germany. angela.yenny@mh-hannover.de.ORCID http://orcid.org/0000-0002-6643-7286
Sebastian HaferkampDepartment of Dermatology, University of Regensburg, Regensburg, Germany.
Carsten WeishauptDepartment of Dermatology, University of Münster, Münster, Germany.
Selma UgurelDepartment of Dermatology, University of Duisburg-Essen, Essen, Germany.
Jürgen C BeckerDepartment of Dermatology, University of Duisburg-Essen, Essen, Germany.
Florian OberndörferDepartment of Dermatology and Allergy, Skin Cancer Center Hannover, Medizinische Hochschule Hannover, Carl Neuberg Str. 1, 30625, Hannover, Germany.
Vesna AlarDepartment of Dermatology and Allergy, Skin Cancer Center Hannover, Medizinische Hochschule Hannover, Carl Neuberg Str. 1, 30625, Hannover, Germany.
Imke SatzgerDepartment of Dermatology and Allergy, Skin Cancer Center Hannover, Medizinische Hochschule Hannover, Carl Neuberg Str. 1, 30625, Hannover, Germany.
Ralf GutzmerDepartment of Dermatology and Allergy, Skin Cancer Center Hannover, Medizinische Hochschule Hannover, Carl Neuberg Str. 1, 30625, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPD-1 inhibition (PD-1i) is the standard of care in melanoma and other malignancies. In patients with bone metastases of solid tumors, the monoclonal antibody denosumab directed against RANKL is approved for the prevention of skeletal-related events. However, RANKL is not only relevant in osteoclastogenesis, but also has immunological effects. Hence, we aimed at investigating, whether the combination of PD-1i and denosumab produces synergistic effects in metastatic melanoma treatment.

methodsWe retrospectively collected and analyzed clinical data of metastatic melanoma patients with bone metastases, who received PD-1i and denosumab therapy.

results29 patients were identified with a median age of 60.7 years: 20 were male and 9 were female. 20 patients (69%) were in stage IV M1c and 9 (31%) in stage IV M1d; 52% had an increased serum LDH. 24 patients (83%) received PD-1i as first-line therapy and five patients (17%) as second- or third-line therapy. 13 patients received the triple combination nivolumab, ipilimumab and denosumab (N + I+D), 16 patients received PD-1i and denosumab (PD-1i + D). Within a median follow-up time of 19.8 months, 17 patients progressed with a median time to progression of 6 months. The objective response rate was 54% in the N + I + D group and 50% in the PD-1i + D group. Recalcification of bone metastases was radiologically observed in 18 (62%) patients. No unexpected treatment-related adverse events emerged.

conclusionsThe combination therapy of metastatic melanoma with PD-1i and denosumab was feasible without unexpected safety issues and showed a promising efficacy signal. Further investigation in prospective studies is needed.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsDenosumabFemaleHumansIpilimumabKaplan-Meier EstimateMaleMelanomaMiddle AgedNivolumabProgrammed Cell Death 1 ReceptorProgression-Free SurvivalDenosumabIpilimumabNivolumabPDCD1 protein, humanProgrammed Cell Death 1 ReceptorRANK LigandTNFSF11 protein, humanAdverse eventsBone metastasisImmunotherapyMelanomaRANK/RANKL

Identifiers

PMID31187176
PMCPMC11028174

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.