Borderline Resectable Pancreatic Cancer: The Importance of This Emerging Stage of Disease

Background Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude immediate surgery. There is no optimal treatment schema for this distinct stage of disease, so the role of surgery is undefined....

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Published inJournal of the American College of Surgeons Vol. 206; no. 5; pp. 833 - 846
Main Authors Katz, Matthew H.G., MD, Pisters, Peter W.T., MD, FACS, Evans, Douglas B., MD, FACS, Sun, Charlotte C., DrPH, MPH, Lee, Jeffrey E., MD, FACS, Fleming, Jason B., MD, FACS, Vauthey, J. Nicolas, MD, FACS, Abdalla, Eddie K., MD, FACS, Crane, Christopher H., MD, Wolff, Robert A., MD, Varadhachary, Gauri R., MD, Hwang, Rosa F., MD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2008
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Abstract Background Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude immediate surgery. There is no optimal treatment schema for this distinct stage of disease, so the role of surgery is undefined. Study Design We defined patients with borderline resectable PA as fitting into one of three distinct groups. Group A comprised patients with tumor abutment of the visceral arteries or short-segment occlusion of the Superior Mesenteric Vein. In group B, patients had findings suggestive but not diagnostic of metastasis. Group C patients were of marginal performance status. Patients were treated initially with chemotherapy, chemoradiation, or both; those of sufficient performance status who completed preoperative therapy without disease progression were considered for surgery. Results Between October 1999 and August 2006, 160 (7%) of 2,454 patients with PA were classified as borderline resectable. Of these, 125 (78%) completed preoperative therapy and restaging, and 66 (41%) underwent pancreatectomy. Vascular resection was required in 18 (27%) of 66 patients, and 62 (94%) underwent a margin-negative pancreatectomy. A partial pathologic response to induction therapy (< 50% viable tumor) was seen in 37 (56%) of 66 patients. Median survival was 40 months for the 66 patients who completed all therapy and 13 months for the 94 patients who did not undergo pancreatectomy (p < 0.001). Conclusions This is the first large report of borderline resectable PA and includes objective definitions for this stage of disease. Our neoadjuvant approach allowed for identification of the marked subset of patients that was most likely to benefit from surgery, as evidenced by the favorable median survival in this group.
AbstractList Background Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude immediate surgery. There is no optimal treatment schema for this distinct stage of disease, so the role of surgery is undefined. Study Design We defined patients with borderline resectable PA as fitting into one of three distinct groups. Group A comprised patients with tumor abutment of the visceral arteries or short-segment occlusion of the Superior Mesenteric Vein. In group B, patients had findings suggestive but not diagnostic of metastasis. Group C patients were of marginal performance status. Patients were treated initially with chemotherapy, chemoradiation, or both; those of sufficient performance status who completed preoperative therapy without disease progression were considered for surgery. Results Between October 1999 and August 2006, 160 (7%) of 2,454 patients with PA were classified as borderline resectable. Of these, 125 (78%) completed preoperative therapy and restaging, and 66 (41%) underwent pancreatectomy. Vascular resection was required in 18 (27%) of 66 patients, and 62 (94%) underwent a margin-negative pancreatectomy. A partial pathologic response to induction therapy (< 50% viable tumor) was seen in 37 (56%) of 66 patients. Median survival was 40 months for the 66 patients who completed all therapy and 13 months for the 94 patients who did not undergo pancreatectomy (p < 0.001). Conclusions This is the first large report of borderline resectable PA and includes objective definitions for this stage of disease. Our neoadjuvant approach allowed for identification of the marked subset of patients that was most likely to benefit from surgery, as evidenced by the favorable median survival in this group.
Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude immediate surgery. There is no optimal treatment schema for this distinct stage of disease, so the role of surgery is undefined. We defined patients with borderline resectable PA as fitting into one of three distinct groups. Group A comprised patients with tumor abutment of the visceral arteries or short-segment occlusion of the Superior Mesenteric Vein. In group B, patients had findings suggestive but not diagnostic of metastasis. Group C patients were of marginal performance status. Patients were treated initially with chemotherapy, chemoradiation, or both; those of sufficient performance status who completed preoperative therapy without disease progression were considered for surgery. Between October 1999 and August 2006, 160 (7%) of 2,454 patients with PA were classified as borderline resectable. Of these, 125 (78%) completed preoperative therapy and restaging, and 66 (41%) underwent pancreatectomy. Vascular resection was required in 18 (27%) of 66 patients, and 62 (94%) underwent a margin-negative pancreatectomy. A partial pathologic response to induction therapy (< 50% viable tumor) was seen in 37 (56%) of 66 patients. Median survival was 40 months for the 66 patients who completed all therapy and 13 months for the 94 patients who did not undergo pancreatectomy (p < 0.001). This is the first large report of borderline resectable PA and includes objective definitions for this stage of disease. Our neoadjuvant approach allowed for identification of the marked subset of patients that was most likely to benefit from surgery, as evidenced by the favorable median survival in this group.
BACKGROUNDPatients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude immediate surgery. There is no optimal treatment schema for this distinct stage of disease, so the role of surgery is undefined.STUDY DESIGNWe defined patients with borderline resectable PA as fitting into one of three distinct groups. Group A comprised patients with tumor abutment of the visceral arteries or short-segment occlusion of the Superior Mesenteric Vein. In group B, patients had findings suggestive but not diagnostic of metastasis. Group C patients were of marginal performance status. Patients were treated initially with chemotherapy, chemoradiation, or both; those of sufficient performance status who completed preoperative therapy without disease progression were considered for surgery.RESULTSBetween October 1999 and August 2006, 160 (7%) of 2,454 patients with PA were classified as borderline resectable. Of these, 125 (78%) completed preoperative therapy and restaging, and 66 (41%) underwent pancreatectomy. Vascular resection was required in 18 (27%) of 66 patients, and 62 (94%) underwent a margin-negative pancreatectomy. A partial pathologic response to induction therapy (< 50% viable tumor) was seen in 37 (56%) of 66 patients. Median survival was 40 months for the 66 patients who completed all therapy and 13 months for the 94 patients who did not undergo pancreatectomy (p < 0.001).CONCLUSIONSThis is the first large report of borderline resectable PA and includes objective definitions for this stage of disease. Our neoadjuvant approach allowed for identification of the marked subset of patients that was most likely to benefit from surgery, as evidenced by the favorable median survival in this group.
Author Evans, Douglas B., MD, FACS
Pisters, Peter W.T., MD, FACS
Wolff, Robert A., MD
Lee, Jeffrey E., MD, FACS
Crane, Christopher H., MD
Fleming, Jason B., MD, FACS
Varadhachary, Gauri R., MD
Hwang, Rosa F., MD
Abdalla, Eddie K., MD, FACS
Katz, Matthew H.G., MD
Vauthey, J. Nicolas, MD, FACS
Sun, Charlotte C., DrPH, MPH
AuthorAffiliation 2 Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
3 Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
1 Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
4 Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
AuthorAffiliation_xml – name: 1 Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
– name: 2 Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
– name: 3 Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
– name: 4 Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
Author_xml – sequence: 1
  fullname: Katz, Matthew H.G., MD
– sequence: 2
  fullname: Pisters, Peter W.T., MD, FACS
– sequence: 3
  fullname: Evans, Douglas B., MD, FACS
– sequence: 4
  fullname: Sun, Charlotte C., DrPH, MPH
– sequence: 5
  fullname: Lee, Jeffrey E., MD, FACS
– sequence: 6
  fullname: Fleming, Jason B., MD, FACS
– sequence: 7
  fullname: Vauthey, J. Nicolas, MD, FACS
– sequence: 8
  fullname: Abdalla, Eddie K., MD, FACS
– sequence: 9
  fullname: Crane, Christopher H., MD
– sequence: 10
  fullname: Wolff, Robert A., MD
– sequence: 11
  fullname: Varadhachary, Gauri R., MD
– sequence: 12
  fullname: Hwang, Rosa F., MD
BackLink https://www.ncbi.nlm.nih.gov/pubmed/18471707$$D View this record in MEDLINE/PubMed
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2008 American College of Surgeons
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Issue 5
Keywords CA 19-9
PA
pancreatic adenocarcinoma
portal vein
superior mesenteric artery
American Joint Committee on Cancer
PV
SMA
AJCC
cancer antigen 19-9
superior mesenteric vein
SMV
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References Evans, Lee, Tamm, Pisters (bib6) 2007
Oken, Creech, Tormey (bib5) 1982; 5
Tseng, Raut, Lee (bib9) 2004; 8
(bib12) 2002
Wolff, Crane, Li (bib2) 2006
Pisters, Hudec, Hess (bib10) 2001; 234
Evans, Rich, Byrd (bib13) 1992; 127
Yen, Abdalla, Pisters, Evans (bib8) 2005
Staley, Cleary, Abbruzzese (bib11) 1996; 12
Raut, Tseng, Sun (bib1) 2007; 246
bib3
Varadhachary, Tamm, Abbruzzese (bib4) 2006; 13
Gallagher, Zervos, Murr (bib7) 2005
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  year: 2005
  end-page: 312
  ident: bib8
  article-title: Pancreaticoduodenectomy
  publication-title: Pancreatic cancer
  contributor:
    fullname: Evans
– volume: 13
  start-page: 1035
  year: 2006
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Snippet Background Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics...
Patients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics that preclude...
BACKGROUNDPatients with borderline resectable pancreatic adenocarcinoma (PA) include those with localized disease who have tumor or patient characteristics...
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StartPage 833
SubjectTerms Adenocarcinoma - classification
Adenocarcinoma - pathology
Adenocarcinoma - surgery
Adenocarcinoma - therapy
Adult
Aged
Aged, 80 and over
Antineoplastic Agents - administration & dosage
Female
Humans
Male
Middle Aged
Neoadjuvant Therapy
Neoplasm Staging
Pancreatectomy
Pancreatic Neoplasms - classification
Pancreatic Neoplasms - pathology
Pancreatic Neoplasms - surgery
Pancreatic Neoplasms - therapy
Radiotherapy
Surgery
Title Borderline Resectable Pancreatic Cancer: The Importance of This Emerging Stage of Disease
URI https://www.clinicalkey.es/playcontent/1-s2.0-S1072751507019813
https://dx.doi.org/10.1016/j.jamcollsurg.2007.12.020
https://www.ncbi.nlm.nih.gov/pubmed/18471707
https://www.proquest.com/docview/69205131/abstract/
https://pubmed.ncbi.nlm.nih.gov/PMC5901743
Volume 206
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