A Prospective Study of Neoadjuvant Gemcitabine Plus Nab-paclitaxel in Patients with Borderline-resectable Pancreatic Cancer.


Journal

Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241

Informations de publication

Date de publication:
01 Feb 2023
Historique:
pubmed: 7 7 2022
medline: 4 2 2023
entrez: 6 7 2022
Statut: ppublish

Résumé

Objectives Neoadjuvant therapy followed by radical resection improves the borderline-resectable pancreatic cancer (BRPC) prognosis; however, the optimal therapeutic regimen remains unclear. Gemcitabine plus nab-paclitaxel (GnP) showed a high anti-tumor effect in primary lesions in a prospective study for metastatic disease. However, evidence concerning its feasibility is still lacking in patients with BRPC. We therefore evaluated the tolerability of neoadjuvant GnP (NAC-GnP) for BRPC. Methods This single-center prospective study evaluated 10 patients with BRPC who were treated with two cycles of NAC-GnP. The primary endpoint was feasibility for NAC-GnP. Treatment feasibility was defined as a successful outcome in at least eight patients. Results Ten patients who had BRPC in contact with the celiac artery (n=5), superior mesenteric artery (n=3), or hepatic artery (n=2) were enrolled. The median age was 75 (range, 40-82) years old. Grade 3 anorexia and grade 2 pneumonia occurred in one patient each, so treatment was feasible in eight patients. The median primary tumor reduction and response rates were 33% (range, 0-68%) and 60%, respectively. Six of eight patients who had abnormal CA19-9 levels at the time of enrolment showed a decrease in CA19-9 levels, with a median decrease of 72%. Five patients underwent radical resection, including R0 resection in four. Postoperative grade IIIa Clavien-Dindo complications occurred in one patient (upper gastrointestinal bleeding and pancreatic fistula). Conclusion Two-cycle NAC-GnP is a feasible treatment for patients with BRPC. Further studies on NAC-GnP in patients with BRPC are warranted.

Identifiants

pubmed: 35793961
doi: 10.2169/internalmedicine.9504-22
pmc: PMC9970803
doi:

Substances chimiques

130-nm albumin-bound paclitaxel 0
Gemcitabine 0
Deoxycytidine 0W860991D6
CA-19-9 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

327-334

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Auteurs

Naohiro Okano (N)

Department of Medical Oncology, Kyorin University Faculty of Medicine, Japan.

Ryota Matsuki (R)

Department of Hepato-Biliary-Pancreatic Surgery, Kyorin University Hospital, Japan.

Masao Toki (M)

Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Japan.

Koichi Gondo (K)

Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Japan.

Kazushige Ochiai (K)

Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Japan.

Shunsuke Watanabe (S)

Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Japan.

Hidekatsu Tateishi (H)

Department of Radiology, Kyorin University Faculty of Medicine, Japan.

Masaharu Kogure (M)

Department of Hepato-Biliary-Pancreatic Surgery, Kyorin University Hospital, Japan.

Yutaka Suzuki (Y)

Department of Hepato-Biliary-Pancreatic Surgery, Kyorin University Hospital, Japan.

Masanori Sugiyama (M)

Tokyo Rosai Hospital, Japan.

Fumio Nagashima (F)

Department of Medical Oncology, Kyorin University Faculty of Medicine, Japan.

Junji Shibahara (J)

Department of Pathology, Kyorin University Faculty of Medicine, Japan.

Yoshihiro Sakamoto (Y)

Department of Hepato-Biliary-Pancreatic Surgery, Kyorin University Hospital, Japan.

Junji Furuse (J)

Department of Medical Oncology, Kyorin University Faculty of Medicine, Japan.

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Classifications MeSH