Evidence map›Paper›PMID 39139592›Full record

ArticleBone reports2024

Are bone targeted agents still useful in times of immunotherapy? The SAKK 80/19 BTA pilot study.

Michael Mark, Alfonso Rojas Mora, Thomas Winder, Anastasios Stathis, Andreas Jakob, Gisela Müller, Stefanie Hayoz, Patrick Reimann, Ulf Petrausch, Roger von Moos and 1 more

Abstract read
In one paragraph

Article in Bone reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Michael MarkDivision of Oncology/Hematology, Cantonal Hospital Graubuenden, Chur, Switzerland.
Alfonso Rojas MoraCompetence Center Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Thomas WinderDepartment of Internal Medicine II, Divison of Oncology/Hematology, Hospital Feldkirch, Feldkirch, Austria.
Anastasios StathisOncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Andreas JakobDivison of Oncology, Hirslanden Aarau, Aarau, Switzerland.
Gisela MüllerCompetence Center Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Stefanie HayozCompetence Center Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Patrick ReimannDepartment of Internal Medicine II, Divison of Oncology/Hematology, Hospital Feldkirch, Feldkirch, Austria.
Ulf PetrauschDivison of Oncology/Hematology, Hirslanden Zurich, Zurich, Switzerland.
Roger von MoosCancer Centre, Cantonal Hospital Graubuenden, Chur, Switzerland.
Swiss Group for Clinical Cancer Research (SAKK)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with bone metastases from solid tumors often have additional treatment with bone targeted agents (BTAs) to avoid symptomatic skeletal events (SSEs) such as clinically significant pathological fracture leading toradiation therapy or surgery to the bone, spinal cord compression, or hypercalcemia. The absolute value of BTA treatment in the era of immunotherapy (IO) is unknown. Methods: Patients with bone metastases treated with immunotherapy within the Alpine Tumor Immunology Registry were compared based on whether they received an additional BTA such as denosumab or zoledronic acid. The primary endpoint was time to first SSE. Continuous data were summarized as median and range, categorical data using frequency counts and percentages. Kaplan-Meier estimates were used to describe and visualize the effect of categorical variables. Results: One hundred and ninety-seven patients with bone metastases and treatment with immunotherapy such as nivolumab (48 %), pembrolizumab (40 %), atezolizumab (12 %), ipilimumab (9 %) and other immunotherapy (5 %) were included. The most frequent tumor types were lung cancer (50 %), malignant melanoma (11 %), renal cell cancer (10 %) and bladder cancer (9 %), respectively. One hundred and twenty-two patients (62 %) received a BTA treatment (91 % denosumab). The median treatment duration of a BTA was 178 days (min: 1 day, max: 2010 days). Out of the 197 patients, 47 (24 %) experienced at least one SSE, 100 (51 %) had bone pain. Ten of the 122 patients (8 %) receiving a BTA developed osteonecrosis of the jaw (ONJ). The percentage of patients without an SSE at fixed time points was higher if treated with a BTA (e.g., at 6 months, 92 % [95 % CI: 84 % - 96 %] versus 88 % [95 % CI: 77 % - 94 %]), but no significant difference in time to first SSE (HR 0.69; 95 % CI 0.34-1.39, log-rank Conclusion: No significant difference in time to first SSE or bone pain was observed between patients who have received a BTA or not when treated with immunotherapy. Based on these retrospective results the indication of BTAs to reduce SSEs in cancer patients under treatment with immunotherapy needs further evaluation.

Indexed as

Bone metastasesBone-targeting agentsImmunotherapySkeletal-related eventsSymptomatic skeletal events

Identifiers

PMID39139592
PMCPMC11321436

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.