Evidence map›Paper›PMID 31601010›Full record

ArticleCancers2019

Sorafenib-Regorafenib Sequential Therapy in Japanese Patients with Unresectable Hepatocellular Carcinoma-Relative Dose Intensity and Post-Regorafenib Therapies in Real World Practice.

Wan Wang, Kaoru Tsuchiya, Masayuki Kurosaki, Yutaka Yasui, Kento Inada, Sakura Kirino, Koji Yamashita, Shuhei Sekiguchi, Yuka Hayakawa, Leona Osawa and 12 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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

22 citing papers in PubMed.

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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

22 authors.

Wan WangDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. w.ou@musashino.jrc.or.jp.
Kaoru TsuchiyaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. tsuchiya@musashino.jrc.or.jp.
Masayuki KurosakiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. kurosaki@musashino.jrc.or.jp.
Yutaka YasuiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. yutakay@musashino.jrc.or.jp.
Kento InadaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. k.inada@musashino.jrc.or.jp.
Sakura KirinoDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. sa.kirino@musashino.jrc.or.jp.
Koji YamashitaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. ykoji1007@yahoo.co.jp.
Shuhei SekiguchiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. s.sekiguch@musashino.jrc.or.jp.
Yuka HayakawaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. y.hayakawa@musashino.jrc.or.jp.
Leona OsawaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. r.oosawa@musashino.jrc.or.jp.
Mao OkadaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. m.okada@musashino.jrc.or.jp.
Mayu HiguchiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. mayu.h@musashino.jrc.or.jp.
Kenta TakauraDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. tuf029@gmail.com.
Chiaki MaeyashikiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. c.maeyashiki@musashino.jrc.or.jp.
Shun KanekoDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. skangast@tmd.ac.jp.
Nobuharu TamakiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. tamaki@musashino.jrc.or.jp.
Hiroyuki NakanishiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. nakanisi@musashino.jrc.or.jp.
Jun ItakuraDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. jitakura@musashino.jrc.or.jp.
Yuka TakahashiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. y.takahashi@musashino.jrc.or.jp.
Yasuhiro AsahinaDepartment of Gastroenterology and Hepatology, Tokyo Medical Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Nobuyuki EnomotoFirst Department of internal Medicine, Faculty of Medicine, University of Yamanashi, Shimokato, Chuo, Yamanashi 409-3898, Japan.
Namiki IzumiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1,Kyonan-cho, Musashino-shi, Tokyo 180-8610, Japan. izumi012@musashino.jrc.or.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to explore the relative dose intensity (RDI) and post-regorafenib treatments in regorafenib therapy.

methodsThe medical records of 38 patients treated with regorafenib between July 2017 and June 2019 at our institution were collected. The RDI of regorafenib for the first month (1M-RDI) was calculated.

resultsThe overall survival (OS) and progression-free survival (PFS) were 12.4 and 3.7 months. The objective response rate and disease control rate were 13.2% and 71.1%. The median total dose of regorafenib in the first month was 2080 mg (240-3360 mg), and the median 1M-RDI was 61.9% (7.1%-100%). Patients with 1M-RDI ≥ 50% showed significantly longer OS and PFS than patients with 1M-RDI < 50% (HR 0.19, 95% CI 0.08-0.48, p = 0.0004 and HR 0.2, 95% CI 0.08-0.52, p = 0.0008). A 1M-RDI ≥ 50% (HR 0.18, 95% CI 0.06-0.55, p = 0.002) and hand-foot skin reaction (HR 0.03, 95% CI 0.008-0.16, p < 0.0001) were independently associated with OS. Post-regorafenib therapies were performed in 19 (86.4%) of 22 patients who had stopped regorafenib due to disease progression.

conclusionA 1M-RDI ≥ 50% is clinically significant. Post-regorafenib therapies are commonly performed in real-world practice.

Indexed as

Hepatocellular carcinomaregorafenibrelative dose intensity (RDI)sequential therapysorafenib

Identifiers

PMID31601010
PMCPMC6826625

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