Recurrent cholangiocarcinoma with long-term survival by multimodal treatment: A case report.

carbon ion radiotherapy chemotherapy cholangiocarcinoma cisplatin gemcitabine hepatic recurrence

Journal

Molecular and clinical oncology
ISSN: 2049-9450
Titre abrégé: Mol Clin Oncol
Pays: England
ID NLM: 101613422

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 08 06 2020
accepted: 09 12 2020
entrez: 18 3 2021
pubmed: 19 3 2021
medline: 19 3 2021
Statut: ppublish

Résumé

Long-term outcomes after surgical resection of bile duct cancer remain unsatisfactory, and survival, particularly after tumor recurrence, is poor. Gemcitabine and cisplatin combination (GC) therapy is the standard first-line treatment; however, second-line approaches are yet to be established. Radiotherapy may prolong the survival of patients with advanced biliary tract cancer, and particle radiotherapy delivers a more concentrated dose than conventional radiotherapy to deeper tumors. The present report describes the long-term survival of a 65-year-old man with distal bile duct cancer of pathological stage IIA (T2N0M0; depth of invasion, 5.5 mm) following multimodal treatment. Following subtotal stomach-preserving pancreatoduodenectomy, multiple hepatic recurrences were identified 9 months later, and GC therapy was initiated. The tumors were no longer evident 18 months later, and GC therapy was discontinued at the patient's request. A computed tomography (CT) scan performed 30 months after surgery identified a new solitary hepatic recurrence and duke pancreatic monoclonal antigen type-2 (DUPAN-2) levels were increased. Further GC therapy was declined. Carbon ion radiotherapy (CIRT) at a dose of 60 Gy [relative biological effectiveness (RBE)-weighted absorbed dose] was then delivered in four fractions over 4 days [15 Gy (RBE)/day]. Tumor size decreased on CT, and fluorodeoxyglucose-positron emission tomography/CT revealed a decline in the standardized uptake value of the tumor after 2 months, with decreased DUPAN-2 levels. Following regrowth of the hepatic recurrence, CIRT was repeated at a dose of 66 Gy (RBE) in four fractions over 4 days [16.5 Gy (RBE)/day] and stable disease was maintained for 19 months. After 19 months, CT revealed tumor regrowth and another new metastatic lesion was identified in the left kidney. The patient received systematic chemotherapy again and died of the disease 81 months after the initial surgery. In conclusion, CIRT is a potential treatment option to control solitary recurrence of biliary tract cancer.

Identifiants

pubmed: 33732458
doi: 10.3892/mco.2021.2234
pii: MCO-0-0-02234
pmc: PMC7907798
doi:

Types de publication

Journal Article

Langues

eng

Pagination

72

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright: © Sota et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Yuki Sota (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Takahiro Einama (T)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Kazuki Kobayashibayashi (K)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Ibuki Fujinuma (I)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Takazumi Tsunenari (T)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Yasuhiro Takihata (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Toshimitsu Iwasaki (T)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Yoichi Miyata (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Koichi Okamoto (K)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Yoshiki Kajiwara (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Eiji Shinto (E)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Hironori Tsujimoto (H)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Shigeo Yasuda (S)

Department of Gastrointestinal Oncology, QST Hospital International Therapy Research Center, Chiba 263-8555, Japan.

Yuka Isozaki (Y)

Department of Gastrointestinal Oncology, QST Hospital International Therapy Research Center, Chiba 263-8555, Japan.

Shigeru Yamada (S)

Department of Gastrointestinal Oncology, QST Hospital International Therapy Research Center, Chiba 263-8555, Japan.

Junji Yamamoto (J)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Hideki Ueno (H)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Yoji Kishi (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Classifications MeSH