Evidence map›Paper›PMID 27234989›Full record

ReviewAdvances in therapy2016

Trabectedin for Soft Tissue Sarcoma: Current Status and Future Perspectives.

Erlinda M Gordon, K Kumar Sankhala, Neal Chawla, Sant P Chawla

4 registry-linked trialsOpen access · hybridAbstract readReview
In one paragraph

Review in Advances in therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
8.2field-weighted citation impact, top 2% 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.

NCT03138161 phase1 / phase2recruitingnot on this mapstarted 2017, after this paper: background citation

SAINT: A Phase 1/2 Study of Safe Amounts of IPLIMUMAB, NIVOLUMAB and TRABECTEDIN for Previously Treated Advanced Soft Tissue Sarcoma (STS)

TypeinterventionalSponsorSarcoma Oncology Research Center, LLCRan2017 to 2031Enrolled250ConditionsAdvanced Soft Tissue Sarcoma, Metastatic Soft Tissue SarcomaArmsTrabectedin, Ipilimumab, Nivolumab
NCT03886311 phase2recruitingnot on this mapstarted 2019, after this paper: background citation

The TNT Protocol: A Phase 2 Study Using Talimogene Laherparepvec,Nivolumab and Trabectedin as First, Second/Third Line Therapy for Advanced Sarcoma, Including Desmoid Tumor and Chordoma

TypeinterventionalSponsorSarcoma Oncology Research Center, LLCRan2019 to 2031Enrolled200ConditionsSarcomaArmsTalimogene Laherparepvec 100000000 PFU/1 ML Injection Suspension [IMLYGIC], Nivolumab IV Soln 100 MG/10ML, Trabectedin 0.25 MG/1 VIAL Intravenous Powder for Solution
NCT04535713 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

GALLANT: A Phase 2 Study Using Metronomic Gemcitabine, Doxorubicin, Docetaxel and Nivolumab as Second/Third Line Therapy for Advanced Sarcoma

TypeinterventionalSponsorSarcoma Oncology Research Center, LLCRan2020 to 2025Enrolled260ConditionsSarcomaArmsGemcitabine, Doxorubicin, Docetaxel, Nivolumab
NCT05876715 phase1 / phase2recruitingnot on this mapstarted 2023, after this paper: background citation

LINNOVATE: A Phase 1/2 Study of Safety/Efficacy Using LURBINECTEDIN, Combined With IPILIMUMAB, and NIVOLUMAB for Advanced Soft Tissue Sarcomas

TypeinterventionalSponsorERLINDA M GORDONRan2023 to 2026Enrolled40ConditionsAdvanced Soft-tissue SarcomaArmsLurbinectedin
3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Macrophages as gatekeepers of glioma progression.Molecular therapy. Oncology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Pegylated liposomal doxorubicin combined with trabectedin as a treatment option in uterine sarcomas: a single-institution retrospective analysis.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Cancers · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Erlinda M GordonSarcoma Oncology Center/Cancer Center of Southern California, Santa Monica, CA, 90403, USA. egordon@sarcomaoncology.com.
K Kumar SankhalaSarcoma Oncology Center/Cancer Center of Southern California, Santa Monica, CA, 90403, USA.
Neal ChawlaSarcoma Oncology Center/Cancer Center of Southern California, Santa Monica, CA, 90403, USA.
Sant P ChawlaSarcoma Oncology Center/Cancer Center of Southern California, Santa Monica, CA, 90403, USA.
Sarcoma Oncology Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledTrabectedin (ET743, Yondelis(®), manufactured by Baxter Oncology GmbH, Halle/Westfalen, Germany, for Janssen Products, LP, Horsham, PA), derived from the marine ascidian, Ecteinascidia turbinata, is a natural alkaloid with multiple complex mechanisms of action. On 23 October 2015, 15 years after the results of the first Phase 1 clinical trial using trabectedin for chemotherapy-resistant solid malignancies was reported, and 8 years after its approval in Europe, the United States Food and Drug Administration (USFDA) finally approved trabectedin for the treatment of unresectable or metastatic liposarcoma or leiomyosarcoma that has failed a prior anthracycline-containing regimen. Approval was based on the results of a pivotal Phase 3 trial involving a 2:1 randomization of 518 patients (who were further stratified by soft tissue sarcoma subtype), in which a significant improvement in progression-free survival was reported in the trabectedin-treated group vs. the dacarbazine-treated group (p < 0.001). In this trial, the most common adverse reactions were nausea, fatigue, vomiting, constipation, anorexia, diarrhea, peripheral edema, dyspnea, and headache, while the most serious were neutropenic sepsis, rhabdomyolysis, cardiomyopathy, hepatotoxicity, and extravasation leading to tissue necrosis. The most common grade 3-4 adverse events were laboratory abnormalities of myelosuppression in both arms and transient transaminitis in the trabectedin arm. In a recent Phase 2 trial, trabectedin had a similar outcome as doxorubicin when given as a single agent in the first-line setting. Studies are also being conducted to expand the use of trabectedin not only as a first-line cancer drug, but also for a number of other clinical indications, for example, in the case of mesenchymal chondrosarcoma, for which trabectedin has been reported to be exceptionally active. The possibility of combining trabectedin with targeted therapies, immune checkpoint inhibitors or virotherapy would also be an interesting concept. In short, trabectedin is an old new drug with proven potential to impact the lives of patients with soft tissue sarcoma and other solid malignancies.

fundingSarcoma Oncology Center, Santa Monica, CA 90405.

Indexed as

Antineoplastic Agents, AlkylatingDioxolesDisease-Free SurvivalEuropeGermanyHumansNeutropeniaRandomized Controlled Trials as TopicSarcomaTetrahydroisoquinolinesTrabectedinAntineoplastic Agents, AlkylatingDioxolesTetrahydroisoquinolinesTrabectedinAlkylating agentChemotherapyClinical trialsDNA minor groove binderET-743OncologySoft tissue sarcomaTrabectedin

Identifiers

PMID27234989
PMCPMC4939148
OpenAlexW2398621244

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.