Optimizing Timing of Intraperitoneal Chemotherapy to Enhance Intravenous Carboplatin Concentration.

carboplatin gastric cancer interval timing intraperitoneal chemotherapy intravenous chemotherapy paclitaxel peritoneal metastases

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
14 Aug 2024
Historique:
received: 09 07 2024
revised: 09 08 2024
accepted: 12 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: epublish

Résumé

Despite advances in systemic chemotherapy, patients with gastric cancer (GC) and peritoneal metastases (PMs) continue to have poor prognoses. Intraperitoneal (IP) administration of Paclitaxel (PTX) combined with systemic chemotherapy shows promise in treating PMs from GC. However, methods of drug administration need to be optimized to maximize efficacy. In this study, we utilized a mouse model with PMs derived from a human GC cell line, administering PTX either IP or intravenously (IV), and Carboplatin (CBDCA) IV 0, 1, and 4 days after PTX administration. The PMs were resected 30 min later, and concentrations of PTX and CBDCA in resected tumors were measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Results indicated that PTX concentrations were higher with IP administration than with IV administration, with significant differences observed on days 0 and 1. CBDCA concentrations 4 days post-IP PTX administration were higher than with simultaneous IV PTX administration. These findings suggest that IP PTX administration enhances CBDCA concentration in peritoneal tumors. Therefore, sequential IV administration of anti-cancer drugs appears more effective than simultaneous administration with IP PTX, a strategy that may improve prognoses for patients with PMs.

Identifiants

pubmed: 39199611
pii: cancers16162841
doi: 10.3390/cancers16162841
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 23H02985

Auteurs

Kohei Tamura (K)

Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi 329-0498, Japan.

Natsuka Kimura (N)

Division of Clinical Pharmacology, Department of Pharmacology, Jichi Medical University, Tochigi 329-0498, Japan.

Hideyuki Ohzawa (H)

Department of Surgery, Jichi Medical University, Tochigi 329-0498, Japan.
Division of Translational Research, Clinical Research Center, Jichi Medical University Hospital, Tochigi 329-0498, Japan.

Hideyo Miyato (H)

Department of Surgery, Jichi Medical University, Tochigi 329-0498, Japan.
Division of Translational Research, Clinical Research Center, Jichi Medical University Hospital, Tochigi 329-0498, Japan.

Naohiro Sata (N)

Department of Surgery, Jichi Medical University, Tochigi 329-0498, Japan.

Takahiro Koyanagi (T)

Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi 329-0498, Japan.

Yasushi Saga (Y)

Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi 329-0498, Japan.

Yuji Takei (Y)

Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi 329-0498, Japan.

Hiroyuki Fujiwara (H)

Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi 329-0498, Japan.

Ryozo Nagai (R)

Jichi Medical University, Tochigi 329-0498, Japan.

Joji Kitayama (J)

Department of Surgery, Jichi Medical University, Tochigi 329-0498, Japan.
Division of Translational Research, Clinical Research Center, Jichi Medical University Hospital, Tochigi 329-0498, Japan.

Kenichi Aizawa (K)

Division of Clinical Pharmacology, Department of Pharmacology, Jichi Medical University, Tochigi 329-0498, Japan.
Division of Translational Research, Clinical Research Center, Jichi Medical University Hospital, Tochigi 329-0498, Japan.
Clinical Pharmacology Center, Jichi Medical University Hospital, Tochigi 329-0498, Japan.

Classifications MeSH