Pancreatic resection for pancreatic carcinoma combined with neo- and adjuvant locoregional targeting immuno-chemotherapy--a prospective randomized study
- PMID: 9638413
Pancreatic resection for pancreatic carcinoma combined with neo- and adjuvant locoregional targeting immuno-chemotherapy--a prospective randomized study
Abstract
Background/aims: The effects on early and late results of combined pancreatic resection with neo- and adjuvant immuno-chemotherapy for patients undergoing pancreatic resection are prospectively evaluated.
Methodology: A group of 26 patients was divided into two groups, which were matched in terms of age-sex ratio, stage of disease, histological diagnosis and mode of pancreatic resection. Group A patients received a multimodality therapy, combining pancreatic resection with neo- and adjuvant locoregional targeting immunochemotherapy. Group B received pancreatic surgery only.
Results: For Group A patients (n = 14pts), a complete response was seen in 11 patients with a time interval ranging from 9 to 29 months. In the remaining 3 patients liver secondaries developed 12 months after pancreatic resection in 2 patients and the other patient developed pulmonary metastases 22 months after pancreatic resection. All patients (n = 3pts) are alive, but continue to have the disease. For Group B patients (n = 12pts), a complete response was seen in 3 patients with a survival of 9, 10 and 20 months following pancreatic resection. Six patients died due to locoregional recurrence of the disease, with the survival rate ranging from 7 to 18 months (mean 10 months). Locoregional recurrence was complicated with liver secondaries (n = 3) and with peritoneal dissemination of the disease in a further 3 patients. The remaining 3 patients are alive, but continue to have the disease due to locoregional recurrence.
Conclusions: Patients in whom neo- and adjuvant locoregional immunochemotherapy was carried out in conjunction with pancreatic resection, demonstrated a significantly higher response rate to treatment. Therefore the data collected offers clear evidence, regarding the usefulness, applicability and safety of combined neo- and adjuvant therapy with pancreatic resection. A Multi-modality approach is therefore highly recommended.
Similar articles
-
Regional targeting chemoimmunotherapy in patients undergoing pancreatic resection in an advanced stage of their disease: a prospective randomized study.Ann Surg. 2002 Dec;236(6):806-13. doi: 10.1097/00000658-200212000-00013. Ann Surg. 2002. PMID: 12454519 Free PMC article. Clinical Trial.
-
Hepatocellular carcinoma: surgical resection versus surgical resection combined with pre- and post-operative locoregional immunotherapy-chemotherapy. A prospective randomized study.Anticancer Res. 1995 Mar-Apr;15(2):543-50. Anticancer Res. 1995. PMID: 7539237 Clinical Trial.
-
Adjuvant therapy following pancreatic resection for pancreatic duct carcinoma: a prospective randomized study.Hepatogastroenterology. 1996 May-Jun;43(9):671-80. Hepatogastroenterology. 1996. PMID: 8799414 Clinical Trial.
-
[Adjuvant treatment of pancreatic cancer].Zentralbl Chir. 2003 May;128(5):411-8. doi: 10.1055/s-2003-40038. Zentralbl Chir. 2003. PMID: 12813641 Review. German.
-
The evolution of adjuvant and neoadjuvant chemotherapy and radiation for advanced pancreatic cancer: from 5-fluorouracil to GTX.Surg Oncol Clin N Am. 2004 Oct;13(4):711-35, x. doi: 10.1016/j.soc.2004.06.005. Surg Oncol Clin N Am. 2004. PMID: 15350944 Review.
Cited by
-
A new method for assaying adhesion of cancer cells to the greater omentum and its application for evaluating anti-adhesion activities of chemically synthesized oligosaccharides.Clin Exp Metastasis. 2000;18(1):37-43. doi: 10.1023/a:1026526829010. Clin Exp Metastasis. 2000. PMID: 11206836
-
Clinical and immune responses to anti-CD3 x anti-EGFR bispecific antibody armed activated T cells (EGFR BATs) in pancreatic cancer patients.Oncoimmunology. 2020 Jun 10;9(1):1773201. doi: 10.1080/2162402X.2020.1773201. Oncoimmunology. 2020. PMID: 32939319 Free PMC article.
-
Inhibition of adhesion and proliferation of peritoneally disseminated tumor cells by pegylated catalase.Clin Exp Metastasis. 2006;23(5-6):269-78. doi: 10.1007/s10585-006-9036-8. Epub 2006 Nov 3. Clin Exp Metastasis. 2006. PMID: 17086358
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical