Risk Analysis for Chemotherapy-induced Nausea and Vomiting (CINV) in Patients Receiving FEC100 Treatment.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 03 06 2019
revised: 30 06 2019
accepted: 02 07 2019
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 8 8 2019
Statut: ppublish

Résumé

Risk factors for chemotherapy-induced nausea and vomiting (CINV) with anthracycline-containing regimen for breast cancer patients remain unknown. The risk factors for CINV with FEC100 were investigated. Data on CINV events and patient backgrounds of 180 patients were collected from the first cycle of FEC100 treatment. In this regimen, patients were administered various antiemetics (ADs). The combinations of ADs were classified into four categories, while body mass index (BMI) was stratified into three categories. Risk factors were selected based on patient characteristics and combination of ADs. Risks for CINV were analyzed by univariate and multivariate analyses. In the univariate analysis of nausea, BMI was a significant factor, while BMI and combination of ADs were significant in vomiting. In the multivariate analysis concerning nausea, BMI was a significant factor. In the analysis concerning vomiting, the combination of ADs and BMI were significant. BMI was the most important risk factor for nausea and vomiting, while the combination of ADs was for vomiting.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Risk factors for chemotherapy-induced nausea and vomiting (CINV) with anthracycline-containing regimen for breast cancer patients remain unknown. The risk factors for CINV with FEC100 were investigated.
PATIENTS AND METHODS METHODS
Data on CINV events and patient backgrounds of 180 patients were collected from the first cycle of FEC100 treatment. In this regimen, patients were administered various antiemetics (ADs). The combinations of ADs were classified into four categories, while body mass index (BMI) was stratified into three categories. Risk factors were selected based on patient characteristics and combination of ADs. Risks for CINV were analyzed by univariate and multivariate analyses.
RESULTS RESULTS
In the univariate analysis of nausea, BMI was a significant factor, while BMI and combination of ADs were significant in vomiting. In the multivariate analysis concerning nausea, BMI was a significant factor. In the analysis concerning vomiting, the combination of ADs and BMI were significant.
CONCLUSION CONCLUSIONS
BMI was the most important risk factor for nausea and vomiting, while the combination of ADs was for vomiting.

Identifiants

pubmed: 31366522
pii: 39/8/4305
doi: 10.21873/anticanres.13596
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

4305-4314

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Mitsuhiro Hayashi (M)

Breast Center, Dokkyo Medical University, Tochigi, Japan hayashim@dokkyomed.ac.jp.

Kyoko Nakazawa (K)

Department of Medical Informatics, Niigata University, Niigata, Japan.

Yoshie Hasegawa (Y)

Department of Breast Surgery, Hirosaki Municipal Hospital, Hirosaki, Japan.

Jun Horiguchi (J)

Department of Breast Surgery, International University of Health and Welfare, Chiba, Japan.

Daishu Miura (D)

Akasaka Miura Clinic, Tokyo, Japan.

Takashi Ishikawa (T)

Department of Breast Oncology, Tokyo Medical University, Tokyo, Japan.

Shintaro Takao (S)

Department of Breast Surgery, Hyogo Cancer Center, Hyogo, Japan.

Seung Jim Kim (SJ)

Department of Breast and Endocrine Surgery, Osaka University, Osaka, Japan.

Kazuhiko Yamagami (K)

Department of Breast Oncology, Shinko Hospital, Hyogo, Japan.

Masaru Miyashita (M)

Department of Surgery, Kohnan Hospital, Hyogo, Japan.

Muneharu Konishi (M)

Department of Surgery, Hyogo Prefectural Nishinomiya Hospital, Hyogo, Japan.

Yasushi Shigeoka (Y)

Department of Medical Oncology, Yodogawa Christian Hospital, Osaka, Japan.

Masato Suzuki (M)

Department of Surgery, National Hospital Organization Chiba Medical Center, Chiba, Japan.

Tetsuya Taguchi (T)

Department of Endocrine and Breast Surgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Tomoyuki Kubota (T)

Department of Surgery, Kamiiida Daiichi General Hospital, Aichi, Japan.

Hirokazu Tanino (H)

Department of Surgery, Kobe University, Hyogo, Japan.

Kimito Yamada (K)

Department of Breast Oncology, Hachioji Medical Center, Tokyo Medical University, Tokyo, Japan.

Kazutaka Narui (K)

Department of Breast and Endocrine Surgery, Yokohama City University Medical Center, Kanagawa, Japan.

Konomi Kimura (K)

Department of Medical Informatics, Niigata University, Niigata, Japan.

Kohei Akazawa (K)

Department of Medical Informatics, Niigata University, Niigata, Japan.

Norio Kohno (N)

Department of Breast Surgery, Kobe Kaisei Hospital, Hyogo, Japan.

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