Evidence map›Paper›PMID 31383985›Full record

Trial reportBritish journal of cancer2019

Survival benefits of dose-dense early postoperative intraperitoneal chemotherapy in front-line therapy for advanced ovarian cancer: a randomised controlled study.

Tingyan Shi, Rong Jiang, Hong Pu, Huijuan Yang, Dongsheng Tu, Zhiyuan Dai, Yunlang Cai, Yuqin Zhang, Xi Cheng, Huixun Jia and 7 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01669226 (A Phase II,Randomized Study of an Addition Intraperitoneal Cisplatin and Etoposide to Standard First-line Therapy in Stage IIIC and Stage IV Epithelial Ovarian, Fallopian Tube, and Primary Peritoneal Cancer), which is not on this map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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.

NCT01669226 phase2completednot on this map

A Phase II,Randomized Study of an Addition Intraperitoneal Cisplatin and Etoposide to Standard First-line Therapy in Stage IIIC and Stage IV Epithelial Ovarian, Fallopian Tube, and Primary Peritoneal Cancer (EOC, FTC, PPC)

TypeinterventionalSponsorShanghai Gynecologic Oncology GroupRan2009 to 2016Enrolled215ConditionsBulky Stage IIIC and IV Epithelial Ovarian Cancer, Fallopian Tube Cancer, Primary Peritoneal CarcinomaArmsPEip (weekly) and TCiv, TCiv
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Innovative landscapes in intraperitoneal therapy of ovarian cancer.Drug delivery and translational research · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. 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

17 authors at 4 institutions in 2 countries.

Tingyan ShiOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China.
Rong JiangOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China.
Hong PuDepartment of Obstetrics and Gynecology, Wuxi Caner Hospital, Jiangsu, China.
Huijuan YangDepartment of Gynecologic Oncology, Fudan University Cancer Hospital, Shanghai, China.
Dongsheng TuDepartment of Mathematics and Statistics, Queen's University, Kingston, Canada.
Zhiyuan DaiDepartment of Obstetrics and Gynecology, Suzhou Municipal Hospital, Jiangsu, China.
Yunlang CaiDepartment of Obstetrics and Gynecology, Zhongda Hospital Southeast University, Jiangsu, China.
Yuqin ZhangOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xi ChengDepartment of Gynecologic Oncology, Fudan University Cancer Hospital, Shanghai, China.
Huixun JiaClinical Statistics Center, Fudan University Cancer Hospital, Shanghai, China.
Ruiqin TuOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China.
Huaying WangDepartment of Gynecologic Oncology, Fudan University Cancer Hospital, Shanghai, China.
Jie TangDepartment of Gynecologic Oncology, Fudan University Cancer Hospital, Shanghai, China.
Yuting LuanOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China.
Shumo CaiDepartment of Gynecologic Oncology, Fudan University Cancer Hospital, Shanghai, China.
Rongyu ZangOvarian Cancer Program, Division of Gynecology Oncology, Department of Obstetrics and Gynecology, Zhongshan Hospital, Fudan University, Shanghai, China. ryzang@yahoo.com.ORCID http://orcid.org/0000-0002-1334-2398
SGOG-OV/AICE Investigators
Fudan University · CNFudan University Shanghai Cancer Center · CNQueen's University · CAZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dose-dense early postoperative intraperitoneal chemotherapy (DD-EPIC) significantly increased non-progression rate in advanced ovarian cancer (OC) patients. We report final overall survival (OS) results to further strengthen the efficacy of DD-EPIC in the front-line therapy. In this phase 2 trial, 218 patients with FIGO IIIC-IV OC were randomly allocated to receive DD-EPIC followed by intravenous (IV) chemotherapy (DD-EPIC group), or IV chemotherapy alone (IV group). The study was prespecified to detect differences in progression-free survival (PFS) and OS. At a median follow-up period of 69.1 months, the median OS was 67.5 and 46.3 months in the DD-EPIC and IV group, respectively. The probability rate of OS at 5 years was 61.0% with DD-EPIC, and 38.2% with IV (hazard ratio [HR] for death from OC, 0.70; 95% confidence interval [CI], 0.49-1.00). DD-EPIC was associated with a prolonged PFS compared with the IV group (the estimated rate of PFS at 5 years, 26.0% vs. 8.5%; HR for disease progression, 0.64; 95% CI, 0.47-0.86). DD-EPIC was associated with a longer OS than IV chemotherapy alone. It may be considered as a valuable option of the front-line therapy for advanced ovarian cancer.Trial registration: ClinicalTrials.gov, NCT01669226 (date of registration: August 20, 2012).

Indexed as

Cytoreduction Surgical ProceduresOvariectomyAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCarcinoma, Ovarian EpithelialChemotherapy, AdjuvantCisplatinDocetaxelEtoposideFemaleHumansInfusions, IntravenousInfusions, ParenteralMiddle AgedCarboplatinCisplatinDocetaxelEtoposidePaclitaxel

Identifiers

PMID31383985
PMCPMC6738091
OpenAlexW2965977634

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.