Evidence map›Paper›PMID 28008452›Full record

Trial reportCancer immunology, immunotherapy : CII2017

Combined treatment with ipilimumab and intratumoral interleukin-2 in pretreated patients with stage IV melanoma-safety and efficacy in a phase II study.

Benjamin Weide, Alexander Martens, Kilian Wistuba-Hamprecht, Henning Zelba, Ludwig Maier, Hans-Peter Lipp, Bernhard D Klumpp, Daniel Soffel, Thomas K Eigentler, Claus Garbe

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer immunology, immunotherapy : CII, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Plasmid DNA ionisable lipid nanoparticles as non-inert carriers and potent immune activators for cancer immunotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Article
  7. Review
  8. Melanoma therapeutics: a literature review.Journal of biomedical research · 2022
    Article
  9. Article
  10. Cytokines: Signalling Improved Immunotherapy?Current oncology reports · 2021
    Review
  11. Review
  12. Cutaneous melanoma and the immunotherapy revolution (Review).International journal of oncology · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Melanoma treatment in review.ImmunoTargets and therapy · 2018
    Review
  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

10 authors.

Benjamin WeideDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany. benjamin.weide@med.uni-tuebingen.de.
Alexander MartensDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Kilian Wistuba-HamprechtDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Henning ZelbaDepartment of Immunology, Institute for Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Ludwig MaierUniversity Hospital Ulm Pharmacy, University Hospital Ulm, Ulm, Germany.
Hans-Peter LippDepartment of Hospital Pharmacy, University Hospital Tübingen, Tübingen, Germany.
Bernhard D KlumppDepartment for Diagnostic and Interventional Radiology, University Hospital Tübingen, Tübingen, Germany.
Daniel SoffelDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Thomas K EigentlerDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Claus GarbeDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of advanced melanoma patients with ipilimumab results in improved survival. However, only about 20% of treated patients experience long-term benefit. Combining treatment of ipilimumab with other drugs may improve immune activation and potentially enhance clinical efficacy. The aims of the phase II clinical trial reported here were to investigate tolerability and efficacy of a combined immunotherapeutic strategy comprising standard systemic ipilimumab at 3 mg/kg four times at 3-week intervals and intratumorally injected IL-2 at 9 MIU daily twice weekly for four weeks in pretreated melanoma patients with distant metastasis. The primary endpoint was the disease control rate according to immune-related response criteria at week 12; tolerability according to Common Terminology Criteria for Adverse Events criteria was secondary endpoint. No objective responses were observed in the 15 enrolled patients. Three patients had stable disease 12 weeks after starting treatment, yielding a disease control rate of 20%. Tolerability of this combination treatment was acceptable. Observed adverse events were those expected from the respective monotherapies. Autoimmune colitis was observed in two patients. Grade III/IV adverse events were observed in 40% of patients, and no treatment-related deaths occurred. Thus, this combined immunotherapy is associated with adverse events similar to those associated with the respective monotherapies. However, this study does not provide any evidence of improved efficacy of the combination over ipilimumab alone.

Indexed as

Antibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsColitisFemaleHumansImmunotherapyInterleukin-2IpilimumabMaleMelanomaMiddle AgedNeoplasm MetastasisNeoplasm StagingProspective StudiesSkin NeoplasmsTreatment OutcomeAntibodies, MonoclonalInterleukin-2IpilimumabClinical trialInterleukin-2IpilimumabMelanoma

Identifiers

PMID28008452
PMCPMC11029278

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.