Evidence map›Paper›PMID 29925345›Full record

Trial reportBMC cancer2018

Induction therapy with paclitaxel and bevacizumab followed by switch maintenance therapy with eribulin in Japanese patients with HER2-negative metastatic breast cancer: a multicenter, collaborative, open-label, phase II clinical study for the SBCCSG 35 investigators.

Kenichi Inoue, Jun Ninomiya, Tsuyoshi Saito, Kei Kimizuka, Masafumi Kurosumi

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 32% 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.

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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Article
  3. Observational
  4. Article
  5. Observational
  6. 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

5 authors at 3 institutions in 1 country.

Kenichi InoueDivision of Breast Oncology, Saitama Cancer Center, 780 Komuro, Ina-machi, Kita-adachi-gun, Saitama, 362-0806, Japan. ino.bad.ken@gmail.com.ORCID http://orcid.org/0000-0003-2686-8732
Jun NinomiyaDepartment of Breast Surgery, Ninomiya Hospital, 2-22-23 Shinei, Soka-shi, Saitama, 340-0056, Japan.
Tsuyoshi SaitoDepartment of Breast Surgery, Japanese Red Cross Saitama Hospital, 1-5 Shintoshin, Chuo-ku, Saitama-shi, Saitama, 330-8553, Japan.
Kei KimizukaDepartment of Breast Surgery, Kasukabe Medical Center, 6-7-1 Chuo, Kasukabe-shi, Saitama, Japan.
Masafumi KurosumiDepartment of Pathology, Saitama Cancer Center, 780 Komuro, Ina-machi, Kita-adachi-gun, Saitama, 362-0806, Japan.
Saitama Cancer Center · JPMorinomiya Hospital · JPSaitama Red Cross Hospital · JP

Funding

Japan Agency for Medical Research and Development 15ck0106046h0002, 15ck0106049h0002National Cancer Center Research and Development Fund 23-A-16, 23-A-17, 26-A-4Research for Innovative Treatment of Cancer from the Ministry of Health, Labour and Welfare H26-applied-general-043,046
6 · The paper itself

Abstract

backgroundTo examine the efficacy and safety of induction therapy with paclitaxel and bevacizumab followed by switch maintenance therapy with eribulin (ISMT) in Japanese patients with HER2-negative metastatic breast cancer (MBC).

methodsPatients, who had previously undergone a maximum of 2 regimens of chemotherapy, received 3 cycles of induction therapy with paclitaxel (90 mg/m

resultsFifty-one eligible patients (median age: 66 years; range: 35-74) were enrolled: 19 (37.3%) and 32 (62.7%) had stage IV and recurrence, respectively, 42 (82.4%) had visceral metastases, and 45 (88.2%) received eribulin-38 of whom showed disease progression, and 40 (78.4%) underwent post therapy. Median TTF was 9.2 months (95% confidence interval [CI]: 7.3-11.1), median progression-free survival was 10.7 months (95% CI: 9.6-11.8), and median overall survival was 20.0 months (95% CI: 16.0-24.0). Relative dose intensity was 97.7% (range: 33.3-100.0) for induction therapy and was 83.3% (range: 49.3-100.6%) for eribulin maintenance therapy. The most common adverse event was alopecia (51 [100%]) in induction therapy and was peripheral sensory neuropathy (37 [82.2%]) in eribulin maintenance therapy. Eribulin was effective with manageable tolerability.

conclusionsISMT may be a promising therapeutic option for patients with MBC.

trial registrationUMIN000015971 . Registration date: January 1, 2015.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsAsian PeopleBevacizumabBreast NeoplasmsFemaleFuransHumansInduction ChemotherapyKaplan-Meier EstimateKetonesMaintenance ChemotherapyMiddle AgedPaclitaxelPolyether PolyketidesBevacizumaberibulinFuransKetonesPaclitaxelPolyether PolyketidesBevacizumabEribulinMetastasisMetastatic breast cancerPaclitaxelSwitch maintenance therapy

Identifiers

PMID29925345
PMCPMC6011527
OpenAlexW2809509361

What OpenQuestion holds

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Registered trials

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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.