Literature DB >> 20811779

Standardization of surgical and pathologic variables is needed in multicenter trials of adjuvant therapy for pancreatic cancer: results from the ACOSOG Z5031 trial.

Matthew H G Katz1, Nipun B Merchant, Steven Brower, Megan Branda, Mitchell C Posner, L William Traverso, Ross A Abrams, Vincent J Picozzi, Peter W T Pisters.   

Abstract

BACKGROUND: Standardization of surgical and pathologic techniques is crucial to the interpretation of studies evaluating adjuvant therapies for pancreatic cancer (PC).
METHODS: To assess the degree to which treatment administered prior to enrollment of patients in trials of adjuvant therapy is quality controlled, the operative and pathology reports of patients in American College of Surgeons Oncology Group (ACOSOG) Z5031-a national trial of chemoradiation following pancreaticoduodenectomy (PD)-were rigorously evaluated. We analyzed variables with the potential to influence staging or outcome.
RESULTS: 80 patients reported to have undergone R0 (75%) or R1 (25%) pylorus-preserving (38%) or standard (62%) PD were evaluated. A search for metastases was documented in 96% of cases. The proximity of the tumor to the superior mesenteric vein was reported in 69%; vein resection was required in 9% and lateral venorrhaphy in 14%. The method of dissection along the superior mesenteric artery (SMA) was described in 68%, being ultrasonic dissection (17%), stapler (24%), and clamp and cut (59%). SMA skeletonization was described in 25%, and absence of disease following resection was documented in 24%. The surgeon reported marking the critical SMA margin in 25%; inking was documented in 65% of cases and evaluation of the SMA margin was reported in 47%. A range of 1-49 lymph nodes was evaluated. Only 34% of pathology reports met College of American Pathologists criteria.
CONCLUSIONS: Trials of adjuvant therapy following PD suffer from a lack of standardization and quality control prior to patient enrollment. These data suggest areas for improvement in the design of multidisciplinary treatment protocols.

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Year:  2010        PMID: 20811779      PMCID: PMC3922125          DOI: 10.1245/s10434-010-1282-y

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  28 in total

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Authors:  Thomas J Howard; Joseph E Krug; Jian Yu; Nick J Zyromski; C Max Schmidt; Lewis E Jacobson; James A Madura; Eric A Wiebke; Keith D Lillemoe
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6.  Redefining the R1 resection in pancreatic cancer.

Authors:  C S Verbeke; D Leitch; K V Menon; M J McMahon; P J Guillou; A Anthoney
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7.  Adjuvant chemoradiotherapy and chemotherapy in resectable pancreatic cancer: a randomised controlled trial.

Authors:  J P Neoptolemos; J A Dunn; D D Stocken; J Almond; K Link; H Beger; C Bassi; M Falconi; P Pederzoli; C Dervenis; L Fernandez-Cruz; F Lacaine; A Pap; D Spooner; D J Kerr; H Friess; M W Büchler
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Journal:  Pancreas       Date:  1996-05       Impact factor: 3.327

9.  Local recurrence following 'curative' surgery for large bowel cancer: I. The overall picture.

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10.  Division of the right posterior attachments of the head of the pancreas with a linear stapler during pancreaticoduodenectomy: vascular and oncological considerations based on an anatomical cadaver-based study.

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Journal:  Surg Radiol Anat       Date:  2008-08-19       Impact factor: 1.246

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  20 in total

1.  Effect of neoadjuvant chemoradiation and surgical technique on recurrence of localized pancreatic cancer.

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Journal:  J Gastrointest Surg       Date:  2011-11-08       Impact factor: 3.452

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4.  Current status of adjuvant therapy for pancreatic cancer.

Authors:  Matthew H G Katz; Jason B Fleming; Jeffrey E Lee; Peter W T Pisters
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Review 5.  Borderline resectable pancreatic cancer: need for standardization and methods for optimal clinical trial design.

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7.  Pancreaticoduodenectomy for pancreatic ductal adenocarcinoma: a French multicentre prospective evaluation of resection margins in 150 evaluable specimens.

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8.  Retroperitoneal dissection in patients with borderline resectable pancreatic cancer: operative principles and techniques.

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9.  Tumour origin and R1 rates in pancreatic resections: towards consilience in pathology reporting.

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10.  Adequacy of pathology reports of specimens from patients with differentiated thyroid cancer.

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