Evidence map›Paper›PMID 32410799›Full record

ArticleChinese journal of cancer research = Chung-kuo yen cheng yen chiu2020

Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group.

Satoshi Takeuchi, Haruo Kuroboshi, Taisuke Mori, Kimihiko Ito, Eiji Kondo, Tsutomu Tabata, Yoshio Itani, Ryuji Kawaguchi, Kyosuke Takeuchi, Toshinori Soejima and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Chinese journal of cancer research = Chung-kuo yen cheng yen chiu, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Satoshi TakeuchiDepartment of Obstetrics and Gynecology, National Hospital Organization Kobe Medical Center, Kobe 6540155, Japan.
Haruo KuroboshiDepartment of Obstetrics and Gynecology, Kyoto Prefectural University of Medicine, Kyoto 6028566, Japan.
Taisuke MoriDepartment of Obstetrics and Gynecology, Kyoto Prefectural University of Medicine, Kyoto 6028566, Japan.
Kimihiko ItoDepartment of Obstetrics and Gynecology, Kansai Rosai Hospital, Amagasaki 6608511, Japan.
Eiji KondoDepartment of Obstetrics and Gynecology, Mie University Graduate Medical School Faculty of Medicine, Tsu, 5148507, Japan.
Tsutomu TabataDepartment of Obstetrics and Gynecology, Mie University Graduate Medical School Faculty of Medicine, Tsu, 5148507, Japan.
Yoshio ItaniDepartment of Obstetrics and Gynecology, Nara Prefectural Nara Hospital (Nara Prefectural General Medical Center), Nara 6308581, Japan.
Ryuji KawaguchiDepartment of Obstetrics and Gynecology, Nara Medical University, Nara 6348521, Japan.
Kyosuke TakeuchiDepartment of Obstetrics and Gynecology, National Hospital Organization Kobe Medical Center, Kobe 6540155, Japan.
Toshinori SoejimaDepartment of Radiation Oncology, Kobe University Graduate School of Medicine, Kobe 6500017, Japan.
Ryohei SasakiDepartment of Obstetrics and Gynecology, National Hospital Organization Kobe Medical Center, Kobe 6540155, Japan.
Hyogo Ion Beam Medical Center · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveConcurrent chemoradiotherapy using cisplatin was thought to be standard treatment for squamous cell carcinoma of cervix, but it had not been effective for adenocarcinoma. Concurrent chemoradiotherapy using irinotecan hydrochloride (CPT-11) had been effective for colorectal cancer, thus, we chose CPT-11 as a candidate for gynecologic adenocarcinoma. To evaluate the maximum tolerated dose (MTD) of weekly CPT-11 with external pelvic radiotherapy, a phase 1/2 study was conducted according to modified Fibonacci method.

methodsEligible patients were advanced uterine cancer with measurable diseases [performance score (PS): 0-2]. Study period was from August 1st, 2002 to December 31st, 2008. The starting dose level (DL) of CPT-11 was 30 mg/m

resultsSeventeen patients were enrolled. As for toxicities, one (1/17: 5.9%) grade (G) 4 neutropenia lasting 7 days had been seen in DL4. G2 diarrhea was identified in 35.3% (6/17) of the patients, and 11.8% (2/17) G3 diarrhea was observed in DL3 and DL4. Thus, the MTD of CPT-11 was defined as dose of 60 mg/m

conclusionsMTD was 60 mg/m

Indexed as

cervical adenocarcinomaConcurrent chemoradiotherapy (CCRT)endometrial canceririnotecan hydrochloride (CPT-11)

Identifiers

PMID32410799
PMCPMC7219098
OpenAlexW3024539135

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.