Evidence map›Paper›PMID 36214925›Full record

ArticleInternational journal of clinical oncology2022

Comparison of treatment outcomes between first-line chemotherapy with or without bevacizumab for advanced ovarian, fallopian tube, and primary peritoneal cancer (Tohoku gynecologic cancer unit: TGCU-RS001 study).

Tadahiro Shoji, Eriko Takatori, Takayuki Nagasawa, Masahiro Kagabu, Tsukasa Baba, Tatsuhiko Shigeto, Yukiko Matsumura, Dai Shimizu, Yukihiro Terada, Manabu Seino and 11 more

Abstract read
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In one paragraph

Article in International journal of clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

21 authors at 7 institutions in 1 country.

Tadahiro ShojiDepartment of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 2-1-1, Idaidori, Yahaba, Iwate, 028-3695, Japan. tshoji@iwate-med.ac.jp.ORCID http://orcid.org/0000-0002-9022-3333
Eriko TakatoriDepartment of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 2-1-1, Idaidori, Yahaba, Iwate, 028-3695, Japan.
Takayuki NagasawaDepartment of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 2-1-1, Idaidori, Yahaba, Iwate, 028-3695, Japan.
Masahiro KagabuDepartment of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 2-1-1, Idaidori, Yahaba, Iwate, 028-3695, Japan.
Tsukasa BabaDepartment of Obstetrics and Gynecology, Iwate Medical University School of Medicine, 2-1-1, Idaidori, Yahaba, Iwate, 028-3695, Japan.
Tatsuhiko ShigetoDepartment of Obstetrics and Gynecology, Hirosaki University School of Medicine, Hirosaki, Japan.
Yukiko MatsumuraDepartment of Obstetrics and Gynecology, Hirosaki University School of Medicine, Hirosaki, Japan.
Dai ShimizuDepartment of Obstetrics and Gynecology, Akita University Graduate School of Medicine, Akita, Japan.
Yukihiro TeradaDepartment of Obstetrics and Gynecology, Akita University Graduate School of Medicine, Akita, Japan.
Manabu SeinoDepartment of Obstetrics and Gynecology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Tsuyoshi OhtaDepartment of Obstetrics and Gynecology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Satoru NagaseDepartment of Obstetrics and Gynecology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Shogo ShigetaDepartment of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hideki TokunagaDepartment of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Muneaki ShimadaDepartment of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Michiko Kaiho-SakumaDepartment of Gynecology, Miyagi Cancer Center, Natori, Japan.
Shigenori FurukawaDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Shu SoedaDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takafumi WatanabeDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Fumiaki TakahashiDepartment of Information Science, Iwate Medical University, Yahaba, Japan.
Yoshihito YokoyamaDepartment of Obstetrics and Gynecology, Hirosaki University School of Medicine, Hirosaki, Japan.
Iwate Medical University · JPFukushima Medical University · JPHirosaki University · JPTohoku University · JPYamagata University · JPAkita University · JPMiyagi Prefectural Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOutcomes with and without bevacizumab as first-line chemotherapy in Japanese-only ovarian cancer patients have not been reported. In this study, we report a retrospective study conducted at the Tohoku Gynecologic Cancer Unit. PATIENTS AND

methodsThe study included 453 patients with stage III/IV ovarian, fallopian tube, and primary peritoneal cancer who received first-line platinum-based chemotherapy. The patients were divided into two groups: bevacizumab (168 patients) and without bevacizumab (285 patients). The primary endpoint was the rate of platinum-resistant recurrence and the secondary endpoints were the antitumor response, progression-free survival, overall survival, and adverse events.

resultsThe objective response rates for patients with measurable diseases treated with and without bevacizumab were 84.5% and 73.0%, respectively (P = 0.0066). Platinum-resistant recurrence in the groups treated with and without bevacizumab was noted in 31 (18.4%) and 111 (38.6%) patients, respectively (P < 0.0001). The median progression-free survival for the bevacizumab and without bevacizumab groups was 23 and 15 months, respectively (P = 0.0002), and the median overall survival was not reached and 49 months, respectively (P = 0.0005). Hypertension of grade 3 or higher was observed in 21 patients (12.5%) in the bevacizumab group (P < 0.001), and proteinuria was observed in 18 patients (10.7%) and 1 patient (0.3%) in the bevacizumab and without bevacizumab groups, respectively (P < 0.001). Intestinal perforation was observed in only one patient (0.6%) in the bevacizumab group.

conclusionCombination and maintenance with bevacizumab in primary chemotherapy for advanced ovarian, fallopian tube, and primary peritoneal cancer was effective in reducing platinum-resistant recurrence rates and prolonging progression-free and overall survival.

Indexed as

Fallopian Tube NeoplasmsOvarian NeoplasmsPeritoneal NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsBevacizumabFallopian TubesFemaleHumansNeoplasm Recurrence, LocalPlatinumProgression-Free SurvivalRetrospective StudiesBevacizumabPlatinumBevacizumabFallopian tubeFirst-line chemotherapyOvarian cancerPlatinum-resistant recurrencePrimary peritoneal cancer

Identifiers

PMID36214925
OpenAlexW4303986625

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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.