Evidence map›Paper›PMID 27418251›Full record

Trial reportBMC cancer2016

Results of sub-analysis of a phase 2 study on trabectedin treatment for extraskeletal myxoid chondrosarcoma and mesenchymal chondrosarcoma.

Hideo Morioka, Shunji Takahashi, Nobuhito Araki, Hideshi Sugiura, Takafumi Ueda, Mitsuru Takahashi, Tsukasa Yonemoto, Hiroaki Hiraga, Toru Hiruma, Toshiyuki Kunisada and 7 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04305548 (Phase II Study on Trabectedin in Advanced Rearranged Mesenchymal Chondrosarcoma), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 11% 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.

NCT04305548 phase2recruitingnot on this mapstarted 2021, after this paper: background citation

Phase II Study on Trabectedin in Advanced Rearranged Mesenchymal Chondrosarcoma

TypeinterventionalSponsorItalian Sarcoma GroupRan2021 to 2026Enrolled16ConditionsMesenchymal ChondrosarcomaArmsTrabectedin
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 43 citations in OpenAlex.

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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

17 authors at 11 institutions in 1 country.

Hideo MoriokaDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan. morioka.z3@keio.jp.
Shunji TakahashiDepartment of Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Nobuhito ArakiDepartment of Orthopaedic Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.
Hideshi SugiuraDepartment of Orthopaedic Surgery, Aichi Cancer Center Hospital, Aichi, Japan.
Takafumi UedaDepartment of Orthopaedic Surgery, Osaka National Hospital, Osaka, Japan.
Mitsuru TakahashiDivision of Orthopaedic Surgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Tsukasa YonemotoDivision of Orthopaedic Surgery, Chiba Cancer Center, Chiba, Japan.
Hiroaki HiragaDepartment of Orthopaedic Surgery, Hokkaido Cancer Center, Hokkaido, Japan.
Toru HirumaDepartment of Musculoskeletal Tumor Surgery, Kanagawa Cancer Center, Kanagawa, Japan.
Toshiyuki KunisadaDepartment of Medical Materials for Musculoskeletal Reconstruction, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.
Akihiko MatsumineDepartment of Orthopedic Surgery, Mie University Graduate School of Medicine, Mie, Japan.
Michiro SusaDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan.
Robert NakayamaDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan.
Kazumasa NishimotoDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan.
Kazutaka KikutaDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan.
Keisuke HoriuchiDepartment of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo, 160-8582, Japan.
Akira KawaiDepartment of Musculoskeletal Oncology, Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
Keio University Hospital · JPAichi Cancer Center · JPChiba Cancer Center · JPHokkaido University Hospital · JPJapanese Foundation For Cancer Research · JPKanagawa Prefectural Hospital Organization · JPMie University · JPOkayama University · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPOsaka National Hospital · JPShizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrabectedin is reported to be particularly effective against translocation-related sarcoma. Recently, a randomized phase 2 study in patients with translocation-related sarcomas unresponsive or intolerable to standard chemotherapy was conducted, which showed clinical benefit of trabectedin compared with best supportive care (BSC). Extraskeletal myxoid chondrosarcoma (EMCS) and Mesenchymal chondrosarcoma (MCS) are very rare malignant soft tissue sarcomas, and are associated with translocations resulting in fusion genes. In addition, the previous in vivo data showed that trabectedin affect tumor necrosis and reduction in vascularization in a xenograft model of a human high-grade chondrosarcoma. The aim of the present analysis was to clarify the efficacy of trabectedin for EMCS and MCS subjects in the randomized phase 2 study.

methodsFive subjects with EMCS and MCS received trabectedin treatment in the randomized phase 2 study. Three MCS subjects were allocated to the BSC group. Objective response and progression-free survival (PFS) were assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by central radiology imaging review.

resultsThe median follow-up time of the randomized phase 2 study was 22.7 months, and one subject with MCS was still receiving trabectedin treatment at the final data cutoff. The median PFS was 12.5 months (95 % CI: 7.4-not reached) in the trabectedin group, while 1.0 months (95 % CI: 0.3-1.0 months) in MCS subjects of the BSC group. The six-month progression-free rate was 100 % in the trabectedin group. One subject with MCS showed partial response, and the others in the trabectedin group showed stable disease. Overall survival of EMCS and MCS subjects was 26.4 months (range, 10.4-26.4 months) in the trabectedin group. At the final data cutoff, two of five subjects were still alive.

conclusionsThis sub-analysis shows that trabectedin is effective for patients with EMCS and MCS compared with BSC. The efficacy results were better than previously reported data of TRS. These facts suggest that trabectedin become an important choice of treatment for patients with advanced EMCS or MCS who failed or were intolerable to standard chemotherapy.

trial registrationThe randomized phase 2 study is registered with the Japan Pharmaceutical Information Center, number JapicCTI-121850 (May 31, 2012).

Indexed as

AdultAgedAntineoplastic Agents, AlkylatingBone NeoplasmsChondrosarcomaChondrosarcoma, MesenchymalDioxolesDisease-Free SurvivalHumansKaplan-Meier EstimateMiddle AgedNeoplasms, Connective and Soft TissueTetrahydroisoquinolinesTrabectedinTreatment OutcomeAntineoplastic Agents, AlkylatingDioxolesTetrahydroisoquinolinesTrabectedinChemotherapyExtraskeletal myxoid chondrosarcomaMesenchymal chondrosarcomaTrabectedinTranslocation-related sarcoma

Identifiers

PMID27418251
PMCPMC4946242
OpenAlexW2460409543

What OpenQuestion holds

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LicenceCC BY
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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.