Evidence map›Paper›PMID 19190632›Full record

Trial reportBritish journal of cancer2009

Gemcitabine-oxaliplatin combination for ovarian cancer resistant to taxane-platinum treatment: a phase II study from the GINECO group.

I Ray-Coquard, B Weber, J Cretin, Z Haddad-Guichard, E Lévy, A C Hardy-Bessard, M C Gouttebel, J-F Geay, A Aleba, H Orfeuvre and 9 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in British journal of cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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.

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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Overcoming platinum resistance in ovarian carcinoma.Expert opinion on investigational drugs · 2010
    Pooled it
  2. A phase 2 study of oxaliplatin combined with continuous infusion topotecan for patients with previously treated ovarian cancer.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2013
    Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Article
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  10. Review
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

19 authors at 13 institutions in 1 country.

I Ray-CoquardCentre Léon Bérard, 28 rue Laennec, 69008 Lyon, France. ray@lyon.fnclcc.fr
B Weber
J Cretin
Z Haddad-Guichard
E Lévy
A C Hardy-Bessard
M C Gouttebel
J-F Geay
A Aleba
H Orfeuvre
C Agostini
J Provencal
J M Ferrero
D Fric
N Dohollou
D Paraiso
J Salvat
E Pujade-Lauraine
GINECO group
Centre Hospitalier de l'Agglomération de Nevers · FRCentre Hospitalier de Niort · FRCentre Léon Bérard · FRHôpital Européen Georges-Pompidou · FRHôtel-Dieu de Paris · FRCentre Antoine Lacassagne · FRCentre Hospitalier Annecy Genevois · FRCentre Hospitalier de Saint-Brieuc · FRCentre Hospitalier Métropole Savoie · FRDélégation Centre-Est · FRHôpital André Mignot · FRInstitut national de recherche en sciences et technologies du numérique · FRPolyclinique de Bordeaux-Tondu · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced ovarian carcinoma in early progression (<6 months) (AOCEP) is considered resistant to most cytotoxic drugs. Gemcitabine (GE) and oxaliplatin (OXA) have shown single-agent activity in relapsed ovarian cancer. Their combination was tested in patients with AOCEP in phase II study. Fifty patients pre-treated with platinum-taxane received q3w administration of OXA (100 mg m(-2), d1) and GE (1000 mg m(-2), d1, d8, 100-min infusion). Patient characteristics were a : median age 64 years (range 46-79),and 1 (84%) or 2 (16%) earlier lines of treatment. Haematological toxicity included grade 3-4 neutropaenia (33%), anaemia (8%), and thrombocytopaenia (19%). Febrile neutropaenia occurred in 3%. Non-haematological toxicity included grade 2-3 nausea or vomiting (34%), grade 3 fatigue (25%),and grade 2 alopecia (24%). Eighteen (37%) patients experienced response. Median progression-free (PF) and overall survivals (OS) were 4.6 and 11.4 months, respectively. The OXA-GE combination has high activity and acceptable toxicity in AOCEP patients. A comparison of the doublet OXA-GE with single-agent treatment is warranted.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDrug Resistance, NeoplasmAgedAntineoplastic AgentsBridged-Ring CompoundsDeoxycytidineDose-Response Relationship, DrugFemaleGemcitabineHumansMiddle AgedOrganoplatinum CompoundsOvarian NeoplasmsOxaliplatinPlatinumTaxoidsAntineoplastic AgentsBridged-Ring CompoundsDeoxycytidineGemcitabineOrganoplatinum CompoundsOxaliplatinPlatinumtaxaneTaxoids

Identifiers

PMID19190632
PMCPMC2653739
OpenAlexW2016069234

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.