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Safety and feasibility of therapeutic anticoagulation for newly diagnosed venous thromboembolism in women who undergo neoadjuvant chemotherapy for advanced ovarian cancer
  1. Thomas Boerner1,
  2. Clarissa Lam1,
  3. Derman Basaran1,
  4. Ying L Liu2,3,
  5. Rachel N Grisham2,3,
  6. William P Tew2,3,
  7. Kara Long Roche1,3,
  8. Oliver Zivanovic1,3,
  9. Nadeem R Abu-Rustum1,3,
  10. Ginger J Gardner1,3,
  11. Yukio Sonoda1,3,
  12. Dennis S Chi1,3,
  13. Gerald Soff2,3,4 and
  14. Elizabeth Jewell1,3
  1. 1Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA
  2. 2Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA
  3. 3Weill Cornell Medical College, New York, NY, USA
  4. 4Division of Hematology, University of Miami Health System, Miami, Florida, USA
  1. Correspondence to Dr Elizabeth Jewell, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; jewelle{at}mskcc.org

Abstract

Objective We sought to investigate the safety and feasibility of therapeutic anticoagulation for newly diagnosed venous thromboembolism among women who undergo neoadjuvant chemotherapy for the treatment of advanced ovarian cancer.

Methods A retrospective study using data extrapolated from a prospectively maintained institutional database was used to identify all patients with ovarian cancer who underwent neoadjuvant chemotherapy from April 2015 through September 2018 at our institution. All patients who received therapeutic anticoagulation for newly diagnosed venous thromboembolism at initial diagnosis or during neoadjuvant chemotherapy were included.

Results Of 290 patients who underwent neoadjuvant chemotherapy for advanced ovarian cancer during the study period, 67 (23%) had newly diagnosed venous thromboembolism at the time of initial diagnosis or developed venous thromboembolism during neoadjuvant chemotherapy. Of these 67 patients, 64 (96%) received therapeutic anticoagulation. A total of 13 (20%) of 64 patients who underwent therapeutic anticoagulation experienced a bleeding episode while on anticoagulation; 4 (31%) of the 13 events were of major severity. Three patients developed major internal bleeding in the peritoneal cavity, and one patient suffered from a major vaginal bleeding episode. All four patients were hospitalized (range, 5–11 days) and received ≥2 units of red blood cells for anemia. None of these patients died from fatal bleeding or had to delay starting chemotherapy. Of note, all four patients received low-molecular-weight heparin via subcutaneous injection. Overall, 13 (20%) of 64 patients required an anticoagulant dose reduction, mostly due to weight loss or new bleeding episodes.

Conclusion Therapeutic anticoagulation in this setting appeared safe, with a low risk of major bleeding complications. Furthermore, anticoagulation did not result in delay of chemotherapy or cytoreductive surgery.

  • ovarian cancer
  • venous thromboembolism

Data availability statement

Data are available upon reasonable request. Data are available from the corresponding author upon reasonable request.

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Data availability statement

Data are available upon reasonable request. Data are available from the corresponding author upon reasonable request.

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Footnotes

  • Contributors Conceptualization: TB, YLL, GS, EJ; Methodology: TB, CL, YLL, GS, EJ; Formal Analysis: TB, CL, YLL, GS, EJ; Investigation: TB, CL, YLL, RG, WT, KL, OZ, NRA-A, GG, YS, DSC, GS, EJ; Data Curation: TB, CL; Visualization: TB, EJ; Supervision: TB, RG, WT, KL, OZ, NRA-A, GG, YS, DSC, EJ; Project Administration: TB, YLL, GS, EJ; Writing - Original Draft: TB, CL, YLL, GS, EJ; Writing - Review and Editing: All authors. EJ is the guarantor.

  • Funding This research was funded in part by the National Institutes of Health/National Cancer Institute Cancer Center Support Grant P30 CA008748.

  • Competing interests Outside the submitted work, YLL reports research funding from GSK, REPARE Therapeutics, and AstraZeneca; RG reports honoraria from GSK, AstraZeneca, Natera, Springworks, Corcept, MJH, and PER; DSC reports personal fees from Apyx Medical, Verthermia Inc., Biom ‘Up, and AstraZeneca, as well as recent or current stock/options ownership of Apyx Medical, Verthemia, Intuitive Surgical, Inc., TransEnterix, Inc., Doximity, Moderna, and BioNTech SE; NRA-R reports research funding paid to the institution by GRAIL; and EJ reports personal fees from Covidien/Medtronic.

  • Provenance and peer review Not commissioned; externally peer reviewed.