Evidence map›Paper›PMID 32749942›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Efficacy of Maintenance Olaparib for Patients With Newly Diagnosed Advanced Ovarian Cancer With a BRCA Mutation: Subgroup Analysis Findings From the SOLO1 Trial.

Paul DiSilvestro, Nicoletta Colombo, Giovanni Scambia, Byoung-Gie Kim, Ana Oaknin, Michael Friedlander, Alla Lisyanskaya, Anne Floquet, Alexandra Leary, Gabe S Sonke and 11 more

Erratum issuedOpen access · greenAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
6.9field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Predictors of long-term progression-free survival in patients with ovarian cancer treated with niraparib in the PRIMA/ENGOT-OV26/GOG-3012 study.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2024
    Trial
  5. Trial
  6. Trial
  7. Trial
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Cancers · 2024
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 20 institutions in 11 countries.

Paul DiSilvestroWomen & Infants Hospital, Providence, RI.
Nicoletta ColomboEuropean Institute of Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), University of Milan-Bicocca, Milan, Italy.
Giovanni ScambiaFondazione Policlinico Universitario A Gemelli, IRCCS, Università Cattolica, Rome, Italy.
Byoung-Gie KimSamsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ana OakninVall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Barcelona, Spain.
Michael FriedlanderUniversity of New South Wales Clinical School, Prince of Wales Hospital, Randwick, New South Wales, Australia.
Alla LisyanskayaSt Petersburg City Oncology Dispensary, St Petersburg, Russia.
Anne FloquetInstitut Bergonié, Comprehensive Cancer Centre, Bordeaux, France.
Alexandra LearyGustave-Roussy Cancer Campus, Villejuif, France.
Gabe S SonkeThe Netherlands Cancer Institute, Amsterdam, the Netherlands.
Charlie GourleyCancer Research UK Edinburgh Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Susana BanerjeeThe Royal Marsden National Health Service Foundation Trust and Institute of Cancer Research, London, United Kingdom.
Amit OzaPrincess Margaret Cancer Centre, Toronto, Ontario, Canada.
Antonio González-MartínClínica Universidad de Navarra, Madrid, Spain.
Carol A AghajanianMemorial Sloan-Kettering Cancer Center, New York, NY.
William H BradleyFroedtert and the Medical College of Wisconsin, Milwaukee, WI.
Cara A MathewsWomen & Infants Hospital, Providence, RI.
Joyce LiuDana-Farber Cancer Institute, Boston, MA.
Elizabeth S LoweAstraZeneca, Gaithersburg, MD.
Ralph BloomfieldAstraZeneca, Cambridge, United Kingdom.
Kathleen N MooreStephenson Cancer Center, University of Oklahoma, Oklahoma City, OK.
Women & Infants Hospital of Rhode Island · USAgostino Gemelli University Polyclinic · ITAstraZeneca (Japan) · JPAstraZeneca (United Kingdom) · GBCity Clinical Oncology Center · RUClinica Universidad de Navarra · ESDana-Farber Cancer Institute · USEdinburgh Cancer Research · GBEuropean Institute of Oncology · ITFroedtert Hospital · USInstitut Bergonié · FRInstitut Gustave Roussy · FRMemorial Sloan Kettering Cancer Center · USNational Health Service · GBOklahoma State University Oklahoma City · USPrince of Wales Hospital · AUPrincess Margaret Cancer Centre · CASamsung Medical Center · KRThe Netherlands Cancer Institute · NLVall d'Hebron Institute of Oncology

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Chief Scientist Office SCD/11NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeIn SOLO1, maintenance olaparib (300 mg twice daily) significantly improved progression-free survival (PFS) for patients with newly diagnosed PATIENTS AND

methodsInvestigator-assessed PFS subgroup analyses of SOLO1 included clinical response after platinum-based chemotherapy (complete [CR] or partial response [PR]), surgery type (upfront or interval surgery), disease status after surgery (residual or no gross residual disease), and BRCA mutation status (

resultsThe risk of disease progression or death was reduced with olaparib compared with placebo by 69% (HR, 0.31; 95% CI, 0.21 to 0.46) and 63% (HR, 0.37; 95% CI, 0.24 to 0.58) in patients undergoing upfront or interval surgery; 56% (HR, 0.44; 95% CI, 0.25 to 0.77) and 67% (HR, 0.33; 95% CI, 0.23 to 0.46) in patients with residual or no residual disease after surgery; 66% (HR, 0.34; 95% CI, 0.24 to 0.47) and 69% in women with clinical CR or PR at baseline (HR, 0.31; 95% CI, 0.18 to 0.52); and 59% (HR, 0.41; 95% CI, 0.30 to 0.56) and 80% (HR 0.20; 95% CI, 0.10 to 0.37) in patients with a

conclusionPatients with newly diagnosed advanced ovarian cancer achieve substantial benefit from maintenance olaparib treatment regardless of baseline surgery outcome, response to chemotherapy, or BRCA mutation type.

Indexed as

BRCA1 ProteinBRCA2 ProteinMutationOvarian NeoplasmsPhthalazinesPiperazinesAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsClinical Trials, Phase III as TopicDouble-Blind MethodFemaleHumansMaintenance ChemotherapyMiddle AgedBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanolaparibOrganoplatinum CompoundsPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID32749942
PMCPMC8190876
OpenAlexW3047016852

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.