Evidence map›Paper›PMID 28933799›Full record

Trial reportThrombosis and haemostasis2017

Rivaroxaban for Preventing Venous Thromboembolism in High-Risk Ambulatory Patients with Cancer: Rationale and Design of the CASSINI Trial. Rationale and Design of the CASSINI Trial.

Alok A Khorana, Saroj Vadhan-Raj, Nicole M Kuderer, Ted Wun, Howard Liebman, Gerald Soff, Chandra Belani, Eileen M O'Reilly, Robert McBane, John Eikelboom and 7 more

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

Trial report in Thrombosis and haemostasis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02555878 (Efficacy and Safety of Rivaroxaban Prophylaxis Compared With Placebo in Ambulatory Cancer Patients Initiating Systemic Cancer Therapy and at High Risk for Venous Thromboembolism), which is not on this map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
8.7field-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.

NCT02555878 phase3completednot on this map

Efficacy and Safety of Rivaroxaban Prophylaxis Compared With Placebo in Ambulatory Cancer Patients Initiating Systemic Cancer Therapy and at High Risk for Venous Thromboembolism

TypeinterventionalSponsorJanssen Research & Development, LLCRan2015 to 2018Enrolled841ConditionsNeoplasmsArmsRivaroxaban, Placebo
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Intravenous thrombolysis in the context of stroke and cancer.Journal of thrombosis and thrombolysis · 2025
    Review
  6. Article
  7. Article
  8. Review
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  11. Tumor-expressed microRNAs associated with venous thromboembolism in colorectal cancer.Research and practice in thrombosis and haemostasis · 2022
    Article
  12. Review
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  18. Review
  19. Concepts in cardiac oncology.European heart journal supplements : journal of the European Society of Cardiology · 2020
    Article
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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 13 institutions in 4 countries.

Alok A KhoranaCleveland Clinic, Cleveland, Ohio, United States.
Saroj Vadhan-RajThe University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States.
Nicole M KudererUniversity of Washington, Seattle, Washington, United States.
Ted WunUniversity of California Davis Comprehensive Cancer Center, Sacramento, California, United States.
Howard LiebmanUniversity of Southern California Keck School of Medicine, Los Angeles, California, United States.
Gerald SoffMemorial Sloan Kettering Cancer Center, New York, New York, United States.
Chandra BelaniPenn State Hershey Cancer Institute, Hershey, Pennsylvania, United States.
Eileen M O'ReillyMemorial Sloan Kettering Cancer Center, New York, New York, United States.
Robert McBaneMayo Clinic, Rochester, Minnesota, United States.
John EikelboomMcMaster University, Hamilton, Ontario, Canada.
C V DamarajuJanssen Research and Development, Raritan, New Jersey, United States.
Karen BeyersJanssen Research and Development, Raritan, New Jersey, United States.
Flavia DietrichJanssen Research and Development, Raritan, New Jersey, United States.
Ajay K KakkarUniversity College London and Thrombosis Research Institute, London, United Kingdom.
Hanno RiessCharité University Hospitals, Berlin, Germany.
Renata D'Alpino PeixotoDepartment of Medical Oncology, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Gary H LymanFred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington, United States.
Janssen (United States) · USMemorial Sloan Kettering Cancer Center · USUniversity of Washington · USBC Cancer Agency · CACharité - Universitätsmedizin Berlin · DECleveland Clinic · USMayo Clinic · USMcMaster University · CAPenn State Milton S. Hershey Medical Center · USThe University of Texas MD Anderson Cancer Center · USThrombosis Research Institute · GBUC Davis Comprehensive Cancer CenterUniversity of Southern California · US

Funding

Risk-adapted thromboprophylaxis of hospitalized cancer patientsR34HL127156 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KHORANA, ALOK A, ZWICKER, JEFFREY · 2016 to 2018
$810k
NHLBI NIH HHS R34 HL127156
6 · The paper itself

Abstract

Venous thromboembolism (VTE) is a frequent complication of cancer associated with morbidity, mortality, increased hospitalizations and higher health care costs. Cancer patients at increased risk for VTE can be identified using a validated risk assessment score, and the incidence of VTE can be reduced in high-risk settings using anticoagulation. Rivaroxaban is a potent, oral, direct, factor Xa inhibitor approved for the prevention and treatment of thromboembolic events, including VTE. CASSINI is a double-blind, randomized, parallel-group, multicentre study comparing rivaroxaban with placebo in adult ambulatory patients with various cancers who are initiating systemic cancer therapy and are at high risk of VTE (Khorana score ≥ 2). Patients with primary brain tumours or those at risk for bleeding are excluded. Approximately 700 patients will be randomized 1:1 to rivaroxaban 10 mg daily or placebo for up to 6 months if there is no evidence of VTE from compression ultrasonography (CU) during screening or from routine care imaging within 30 days prior to randomization. Mandatory CU will also be performed at weeks 8 and 16 (±7 days), and at study end (±3 days). The primary efficacy hypothesis is that anticoagulation with rivaroxaban reduces the composite of objectively confirmed symptomatic or asymptomatic, lower-extremity, proximal deep-vein thrombosis (DVT); symptomatic, upper-extremity DVT; symptomatic or incidental pulmonary embolism; and VTE-related death compared with placebo. The primary safety objective is to assess major bleeding events (Clinical trial information: NCT02555878).

Indexed as

Ambulatory CareBlood CoagulationClinical ProtocolsDouble-Blind MethodEuropeFactor Xa InhibitorsFemaleHemorrhageHumansMaleNeoplasmsNorth AmericaPulmonary EmbolismResearch DesignRisk FactorsRivaroxabanFactor Xa InhibitorsRivaroxabananticoagulation risk stratification rivaroxaban venous thromboembolism neoplasms prophylaxis

Identifiers

PMID28933799
PMCPMC6328370
OpenAlexW2759791460

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.