Evidence map›Paper›PMID 31811519›Full record

ArticleBreast cancer (Tokyo, Japan)2020

Factors associated with prolonged overall survival in patients with postmenopausal estrogen receptor-positive advanced breast cancer using real-world data: a follow-up analysis of the JBCRG-C06 Safari study.

Hidetoshi Kawaguchi, Norikazu Masuda, Takahiro Nakayama, Kenjiro Aogi, Keisei Anan, Yoshinori Ito, Shoichiro Ohtani, Nobuaki Sato, Shigehira Saji, Toshimi Takano and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Breast cancer (Tokyo, Japan), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

  1. Pooled it
  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

23 authors.

Hidetoshi KawaguchiDepartment of Breast Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama, 790-8524, Japan. hkawaguchi@matsuyama.jrc.or.jp.ORCID http://orcid.org/0000-0002-0811-9335
Norikazu MasudaDepartment of Surgery, Breast Oncology, NHO Osaka National Hospital, Osaka, 540-0006, Japan.
Takahiro NakayamaDepartment of Breast and Endocrine Surgery, Osaka International Cancer Institute, Osaka, 541-8567, Japan.
Kenjiro AogiDepartment of Breast Oncology, NHO Shikoku Cancer Center, Matsuyama, 791-0280, Japan.
Keisei AnanDepartment of Surgery, Kitakyushu Municipal Medical Center, Kitakyushu, 802-0077, Japan.
Yoshinori ItoDepartment of Breast Medical Oncology, The Cancer Institute Hospital of JFCR, Tokyo, 135-8550, Japan.
Shoichiro OhtaniDepartment of Breast Surgery, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, 730-8518, Japan.
Nobuaki SatoDepartment of Breast Oncology, Niigata Cancer Center Hospital, Niigata, 951-8566, Japan.
Shigehira SajiDepartment of Medical Oncology, Fukushima Medical University, Fukushima, 960-1295, Japan.
Toshimi TakanoDepartment of Medical Oncology, Toranomon Hospital, Tokyo, 105-8470, Japan.
Eriko TokunagaDepartment of Breast Oncology, Kyushu Cancer Center, Fukuoka, 811-1395, Japan.
Seigo NakamuraDepartment of Surgery, Division of Breast Surgical Oncology, Showa University School of Medicine, Tokyo, 142-8666, Japan.
Yoshie HasegawaDepartment of Breast Surgery, Hirosaki Municipal Hospital, Hirosaki, 036-8004, Japan.
Masaya HattoriDepartment of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, 464-8681, Japan.
Tomomi FujisawaDepartment of Breast Oncology, Gunma Prefectural Cancer Center, Ohta, 373-8550, Japan.
Satoshi MoritaDepartment of Biomedical Statistics and Bioinformatics, Graduate School of Medicine, Kyoto University, Kyoto, 606-8507, Japan.
Miki YamaguchiDepartment of Breast Surgery, JCHO Kurume General Hospital, Kurume, 830-0013, Japan.
Hiroko YamashitaDepartment of Breast Surgery, Hokkaido University Hospital, Sapporo, 060-8648, Japan.
Toshinari YamashitaDepartment of Breast and Endocrine Surgery, Kanagawa Cancer Center, Yokohama, 241-8515, Japan.
Yutaka YamamotoDepartment of Breast and Endocrine Surgery, Kumamoto University Graduate School of Medical Sciences, Kumamoto, 860-8556, Japan.
Daisuke YotsumotoDepartment of Breast Surgical Oncology, Hakuaikai Medical Corporation Sagara Hospital, Kagoshima, 892-0833, Japan.
Masakazu ToiDepartment of Breast Surgery, Graduate School of Medicine, Kyoto University, Kyoto, 606-8507, Japan.
Shinji OhnoBreast Oncology Center, The Cancer Institute Hospital of JFCR, Tokyo, 135-8550, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAssessing survival risk is important for discussing treatment options with estrogen receptor-positive (ER+) advanced breast cancer (ABC) patients. However, there are few reports from large-scale databases on the survival risk factors in ER+ ABC. The Safari study (UMIN000015168) was a retrospective, multicenter cohort study involving 1072 Japanese patients receiving fulvestrant 500 mg mostly as a second- or later-line endocrine therapy for ER+ ABC. The follow-up data after the Safari study were examined, focusing on any relationship between clinicopathological factors and overall survival (OS) in ER+ ABC patients.

methodsOS in patients with ER+ ABC was analyzed by univariate and multivariate analyses with a Cox proportional hazards model in this study.

resultsA total of 1031 cases were evaluable for OS analysis. Multivariate analysis showed that younger age (< 60 years), longer time from ABC diagnosis to fulvestrant use (≥ 3 years), no prior palliative chemotherapy before fulvestrant use, and progesterone receptor (PgR) negativity (PgR-) were significantly correlated with prolonged OS (median 7.0 years). For cases with histological or nuclear grade data, lower histological or nuclear grades were also correlated with longer OS. In recurrent metastatic cases, long disease-free interval (DFI) was not correlated with longer OS.

conclusionsIn ER+ ABC patients whose treatment history included fulvestrant, younger age, longer time from ABC diagnosis to fulvestrant use, no prior palliative chemotherapy use, PgR-, and lower histological or nuclear grade correlated positively with prolonged OS.

Indexed as

PostmenopauseAdultAgedAged, 80 and overAntineoplastic Agents, HormonalBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesFulvestrantHumansMiddle AgedNeoplasm Recurrence, LocalPrognosisAntineoplastic Agents, HormonalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFulvestrantReceptors, EstrogenReceptors, ProgesteroneAntineoplastic agentsBreast cancerHormonesOverall survivalPost-menopause

Identifiers

PMID31811519
PMCPMC7196081

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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.