Clinical Outcome of Ampullary Carcinoma: Single Cancer Center Experience.


Journal

Journal of oncology
ISSN: 1687-8450
Titre abrégé: J Oncol
Pays: Egypt
ID NLM: 101496537

Informations de publication

Date de publication:
2019
Historique:
received: 11 11 2018
revised: 20 02 2019
accepted: 21 03 2019
entrez: 13 6 2019
pubmed: 13 6 2019
medline: 13 6 2019
Statut: epublish

Résumé

Ampullary cancers represent a subset of periampullary cancers, comprising only 0.2% all gastrointestinal cancers. Localized disease is primarily managed by a surgical intervention, called pancreaticoduodenectomy (PD), followed in many cases by the administration of adjuvant chemotherapy (CT) or chemoradiation therapy (CRT). However, there are no clear evidence-based guidelines to aid in selecting both the modality and regimen of adjuvant therapy for resected Ampullary carcinoma. We retrospectively analyzed 54 patients at KU Cancer Center, who had undergone endoscopic resection or pancreaticoduodenectomy (PD) for Ampullary cancer from June 2006 to July 2016. We obtained patients' baseline characteristics, clinical presentation, pathology, treatment modality, recurrence pattern, and survival outcomes. The time-to-events data were compared using Kaplan-Meier methods. A univariate and multivariate Cox proportional hazards regression was performed to evaluate factors associated with overall survival (OS) and generate hazard ratios (HR). The mean age of the 54 patients was 68 (37-90). 38 (70%) were males and 16 (30%) were females. Most of the patients were Caucasian (76%). Approximately half of all patients had a history of smoking, 20% had alcohol abuse, and 13% had pancreatitis. Among the 54 patients with localized cancers, 9 (16%) were treated definitively with nonoperative therapies, usually due to a prohibitive comorbidity profile, performance status, or unresectable tumor. 45 out of 54 patients (83%) underwent surgery. Of the 45 patients who underwent surgery, 18 patients (40% of the study cohort) received adjuvant therapy due to concerns for advanced disease as determined by the treating physician. 13 patients (24%) received adjuvant CT and 5 patients (9.2%) received CRT. The remaining 27 patients (50%) underwent surgery alone. The median OS for the entire study cohort was 30 months. When compared to surgery alone, adjuvant therapy with either CT or CRT had no statistically significant difference in terms of progression-free survival ( Despite numerous advances in both cancer care and research, efforts in rare malignancies such as Ampullary cancer remain very challenging with a clear lack of an evidence-based standard of care treatment paradigm. Although adding adjuvant therapies such as chemotherapy or chemoradiotherapy is likely to improve survival in high-risk disease, there is no standardized regimen for the treatment of Ampullary cancer. More research is required to elucidate whether statistically and clinically relevant differences exist that may warrant a change in the current adjuvant treatment strategies.

Identifiants

pubmed: 31186632
doi: 10.1155/2019/3293509
pmc: PMC6521487
doi:

Types de publication

Journal Article

Langues

eng

Pagination

3293509

Références

Ann Surg. 1999 Dec;230(6):776-82; discussion 782-4
pubmed: 10615932
Int J Radiat Oncol Biol Phys. 2000 Jul 1;47(4):945-53
pubmed: 10863064
Eur J Surg Oncol. 2005 Mar;31(2):158-63
pubmed: 15698732
Int J Radiat Oncol Biol Phys. 2006 Oct 1;66(2):514-9
pubmed: 16863684
Ann Surg Oncol. 2008 Jul;15(7):1820-7
pubmed: 18369675
Ann Oncol. 2009 May;20 Suppl 4:46-8
pubmed: 19454460
J Surg Oncol. 2009 Dec 1;100(7):598-605
pubmed: 19697352
J Gastrointest Surg. 2010 Feb;14(2):379-87
pubmed: 19911239
Radiat Oncol. 2011 Sep 28;6:126
pubmed: 21951377
JAMA. 2012 Jul 11;308(2):147-56
pubmed: 22782416
J Am Coll Surg. 2012 Aug;215(2):e11-8
pubmed: 22818108
ANZ J Surg. 2015 Jul-Aug;85(7-8):567-71
pubmed: 24735093
Ann Surg. 2015 Jul;262(1):47-52
pubmed: 25775067
World J Gastroenterol. 2015 Jul 14;21(26):7970-87
pubmed: 26185369
Mod Pathol. 2016 Dec;29(12):1575-1585
pubmed: 27586202
Ann Surg Oncol. 2017 Jul;24(7):2031-2039
pubmed: 28124275
Pancreatology. 2017 Mar - Apr;17(2):273-278
pubmed: 28131524
Am J Surg. 2017 Nov;214(5):856-861
pubmed: 28285709
Clin Transl Oncol. 2018 Sep;20(9):1212-1218
pubmed: 29497964
Cancer. 1988 Apr 1;61(7):1394-402
pubmed: 3422832
Arch Surg. 1996 Apr;131(4):366-71
pubmed: 8615720
Ann Surg. 1997 May;225(5):590-9; discussion 599-600
pubmed: 9193186

Auteurs

Mohammed Al-Jumayli (M)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Amna Batool (A)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Akshay Middiniti (A)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Anwaar Saeed (A)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Weijing Sun (W)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Raed Al-Rajabi (R)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Joaquina Baranda (J)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Sean Kumer (S)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Timothy Schmitt (T)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Anusha Chidharla (A)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Anup Kasi (A)

Division of Medical Oncology, KU Cancer Center, The University of Kansas Health System, USA.

Classifications MeSH