Evidence map›Paper›PMID 28763145›Full record

Trial reportCancer science2017

Phase II study of S-1 plus leucovorin in patients with metastatic colorectal cancer: Regimen of 1 week on, 1 week off.

Jin Li, Ruihua Xu, Jianming Xu, Tadamichi Denda, Koji Ikejiri, Lin Shen, Yasushi Toh, Ken Shimada, Takeshi Kato, Kenji Sakai and 4 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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

14 authors.

Jin LiDepartment of Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0001-5523-0055
Ruihua XuDivision of Oncology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong Province, China.
Jianming XuNo. 4 Division of Oncology, People's Liberation Army No. 307 Hospital, Beijing, China.
Tadamichi DendaDivision of Gastroenterology, Chiba Cancer Center, Chiba City, Japan.
Koji IkejiriDepartment of Surgery, Gastroenterology Center, National Hospital Organization Kyushu Medical Center, Fukuoka City, Japan.
Lin ShenDigestive System Medicine Department, Beijing Cancer Hospital, Beijing, China.
Yasushi TohDepartment of Gastroenterological Surgery, National Hospital Organization, National Kyushu Cancer Center, Fukuoka City, Japan.
Ken ShimadaDepartment of Internal Medicine, Showa University Northern Yokohama Hospital, Yokohama City, Japan.
Takeshi KatoDepartment of Surgery, Minoh City Hospital, Minoh City, Japan.
Kenji SakaiDepartment of Medical Oncology, Saiseikai Kumamoto Hospital, Kumamoto City, Japan.
Manabu YamamotoDepartment of Surgery, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima City, Japan.
Hideyuki MishimaDepartment of Surgery, National Hospital Organization Osaka National Hospital, Osaka City, Japan.
Jinwan WangDivision of Oncology, Chinese Institute & Hospital Chinese Academy of Medical Sciences, Beijing, China.
Hideo BabaGastroenterological Surgery, Kumamoto University Hospital, Kumamoto City, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A phase II study of S-1 plus leucovorin (LV) given in a 4-week schedule (2 weeks' administration followed by 2 weeks' rest) for patients with untreated metastatic colorectal cancer (mCRC) showed that the combination was effective, but grade 3 toxicities (diarrhea, stomatitis and anorexia) occurred at a relatively high rate. In this phase II study, we evaluated the efficacy and safety of a 2-week schedule of S-1 plus LV. Patients with mCRC received oral S-1 (40-60 mg) and LV (25 mg) twice daily for 1 week, followed by 1 week's rest. Treatment was repeated until disease progression or unacceptable toxicity. The primary endpoint was response rate. The pharmacokinetics of S-1 and LV in Chinese patients were evaluated on day 1 of the first cycle. Seventy-three patients were enrolled in Japan and China. Of 71 eligible patients, the response rate was 53.5%, and the disease control rate was 83.1%. Median progression-free survival and median overall survival were 6.5 and 24.3 months, respectively. The incidences of grade 3 toxicities were diarrhea 8.3%, stomatitis 8.3%, anorexia 2.8% and neutropenia 9.7%. There were no treatment-related deaths. The pharmacokinetics profiles of S-1 plus LV in Chinese patients were similar to those in Japanese patients. This 2-week schedule of S-1 plus LV showed good efficacy and better tolerability than the 4-week schedule. This therapy will be the base regimen for mCRC to be added by other cytotoxic or molecular-targeted drugs. The optimized treatment schedule for S-1 plus LV was 1 week on and 1 week off.

Indexed as

AdultAgedAged, 80 and overAnorexiaAntineoplastic Combined Chemotherapy ProtocolsChinaColorectal NeoplasmsDiarrheaDrug Administration ScheduleDrug CombinationsFemaleHumansJapanLeucovorinMaleMiddle AgedDrug CombinationsLeucovorinOxonic AcidS 1 (combination)TegafurClinical trialcolorectal neoplasmsleucovorinpharmacokineticsS-1 (combination)

Identifiers

PMID28763145
PMCPMC5623741

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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.