Evidence map›Paper›PMID 28489919›Full record

ArticlePloS one2017

Efficacy and safety of gemcitabine plus docetaxel in Japanese patients with unresectable or recurrent bone and soft tissue sarcoma: Results from a single-institutional analysis.

Masanobu Takahashi, Keigo Komine, Hiroo Imai, Yoshinari Okada, Ken Saijo, Masahiro Takahashi, Hidekazu Shirota, Hisatsugu Ohori, Shin Takahashi, Natsuko Chiba and 3 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. lncRNAOncology letters · 2021
    Article
  9. Systemic Options for Malignant Peripheral Nerve Sheath Tumors.Current treatment options in oncology · 2021
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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

13 authors.

Masanobu TakahashiDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Keigo KomineDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Hiroo ImaiDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Yoshinari OkadaDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Ken SaijoDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Masahiro TakahashiDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Hidekazu ShirotaDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Hisatsugu OhoriDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Shin TakahashiDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Natsuko ChibaDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Takahiro MoriDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Hideki ShimodairaDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.
Chikashi IshiokaDepartment of Medical Oncology, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.ORCID http://orcid.org/0000-0002-3023-1227

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCombination therapy with gemcitabine and docetaxel has been reported to be a good therapeutic strategy for patients with soft tissue sarcoma. The aim of the present study was to analyze the efficacy and toxicity of gemcitabine with docetaxel in Japanese patients with advanced bone and soft tissue sarcoma. PATIENTS AND

methodsWe retrospectively analyzed the effect of gemcitabine and docetaxel therapy on overall response, progression-free survival, overall survival, and toxicity in 42 patients with bone or soft tissue sarcoma who had received the therapy between October 2006 and September 2015, at Tohoku University Hospital.

resultsThe median age was 55 years; 23 patients were men, and 19 were women. Eight had bone sarcoma and 34 had soft tissue sarcoma. Forty patients (95%) had previously been treated with one or more chemotherapeutic regimens. The overall response rate was 6.9% and the disease control rate was 55%. The median progression-free survival was 2.3 months and the median overall survival was 14.3 months. Grade 3 or more neutropenia and febrile neutropenia were observed in 74% and 4.8% of all patients, respectively.

conclusionThe response rate was lower and myelosuppression was more frequently observed than in other previous reports. On the other hand, most of toxicities were enough manageable. In addition, some patients had long survival with a good response. Our study supports the notion that gemcitabine and docetaxel therapy is a good therapeutic option for treating patients with advanced soft tissue sarcoma as well as bone sarcoma, also in Asian populations.

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticAntineoplastic AgentsBone NeoplasmsDeoxycytidineDisease-Free SurvivalDocetaxelDrug Administration ScheduleDrug Therapy, CombinationFemaleGemcitabineHumansJapanMaleAntimetabolites, AntineoplasticAntineoplastic AgentsDeoxycytidineDocetaxelGemcitabineTaxoids

Identifiers

PMID28489919
PMCPMC5425189

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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.