Venous thromboembolism in cancer patients: report of baseline data from the multicentre, prospective Cancer-VTE Registry.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
22 Oct 2020
Historique:
received: 14 04 2020
accepted: 26 06 2020
pubmed: 28 7 2020
medline: 13 11 2020
entrez: 28 7 2020
Statut: ppublish

Résumé

The Cancer-VTE Registry evaluates the occurrence and management of venous thromboembolism in Japanese participants with major solid tumors. Using Registry data, we evaluated the frequency of concurrent venous thromboembolism in cancer patients prior to treatment initiation by cancer type. The Cancer-VTE Registry is an ongoing (March 2017-September 2020) prospective cohort study using a nationwide, multicentre clinical registry. Participants aged ≥20 years with colorectal, lung, stomach, pancreatic, breast or gynecologic cancer, confirmed staging, ≥6 months life expectancy post-registration and who had undergone venous thromboembolism screening were managed with routine clinical care. Venous thromboembolism frequency at registration was evaluated. Of 9735 participants, 571 (5.9%) had venous thromboembolism at baseline, including asymptomatic [5.5% (n = 540)] and symptomatic venous thromboembolism [0.3% (n = 31)]. Most participants with venous thromboembolism (n = 506, 5.2%) had deep vein thrombosis only; 65 (0.7%) had pulmonary embolism with/without deep vein thrombosis. The prevalence of distal and proximal deep vein thrombosis was 4.8% (n = 466) and 0.9% (n = 83), respectively. The highest prevalence of venous thromboembolism was for pancreatic cancer (8.5%) and the lowest for breast cancer (2.0%). Venous thromboembolism prevalence increased as cancer stage advanced. Although there was a marked difference in venous thromboembolism by cancer type, the data suggest that cancer stage is an important risk factor for venous thromboembolism. Thus, metastasis seems a critical risk factor for venous thromboembolism. This is the first demonstration of venous thromboembolism prevalence and risk factors in Japanese cancer patients prior to treatment. UMIN000024942.

Sections du résumé

BACKGROUND BACKGROUND
The Cancer-VTE Registry evaluates the occurrence and management of venous thromboembolism in Japanese participants with major solid tumors. Using Registry data, we evaluated the frequency of concurrent venous thromboembolism in cancer patients prior to treatment initiation by cancer type.
METHODS METHODS
The Cancer-VTE Registry is an ongoing (March 2017-September 2020) prospective cohort study using a nationwide, multicentre clinical registry. Participants aged ≥20 years with colorectal, lung, stomach, pancreatic, breast or gynecologic cancer, confirmed staging, ≥6 months life expectancy post-registration and who had undergone venous thromboembolism screening were managed with routine clinical care. Venous thromboembolism frequency at registration was evaluated.
RESULTS RESULTS
Of 9735 participants, 571 (5.9%) had venous thromboembolism at baseline, including asymptomatic [5.5% (n = 540)] and symptomatic venous thromboembolism [0.3% (n = 31)]. Most participants with venous thromboembolism (n = 506, 5.2%) had deep vein thrombosis only; 65 (0.7%) had pulmonary embolism with/without deep vein thrombosis. The prevalence of distal and proximal deep vein thrombosis was 4.8% (n = 466) and 0.9% (n = 83), respectively. The highest prevalence of venous thromboembolism was for pancreatic cancer (8.5%) and the lowest for breast cancer (2.0%). Venous thromboembolism prevalence increased as cancer stage advanced.
CONCLUSIONS CONCLUSIONS
Although there was a marked difference in venous thromboembolism by cancer type, the data suggest that cancer stage is an important risk factor for venous thromboembolism. Thus, metastasis seems a critical risk factor for venous thromboembolism. This is the first demonstration of venous thromboembolism prevalence and risk factors in Japanese cancer patients prior to treatment.
TRIAL REGISTRATION BACKGROUND
UMIN000024942.

Identifiants

pubmed: 32715307
pii: 5876093
doi: 10.1093/jjco/hyaa112
pmc: PMC7579341
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1246-1253

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press.

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Auteurs

Yasuo Ohashi (Y)

Department of Integrated Science and Engineering for Sustainable Society, Chuo University, Tokyo, Japan.

Masataka Ikeda (M)

Division of Lower Gastrointestinal Surgery, Hyogo College of Medicine, Nishinomiya, Japan.

Hideo Kunitoh (H)

Department of Medical Oncology, Japanese Red Cross Medical Center, Tokyo, Japan.

Mitsuru Sasako (M)

Department of Surgery, Yodogawa Christian Hospital, Osaka, Japan.

Takuji Okusaka (T)

Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.

Hirofumi Mukai (H)

Division of Breast and Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Keiichi Fujiwara (K)

Department of Gynecologic Oncology, Saitama Medical University International Medical Center, Hidaka, Japan.

Mashio Nakamura (M)

Department of Internal Medicine, Pediatrics and Cardiology, Nakamura Medical Clinic, Kuwana, Japan.

Mari S Oba (MS)

Department of Medical Statistics, Faculty of Medicine, Toho University, Tokyo, Japan.

Tetsuya Kimura (T)

Medical Science Department, Daiichi Sankyo Co. Ltd., Tokyo, Japan.

Kei Ibusuki (K)

Medical Science Department, Daiichi Sankyo Co. Ltd., Tokyo, Japan.

Masato Sakon (M)

Department of Gastrointestinal Surgery, Osaka International Cancer Institute, Osaka, Japan.

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