By: SUSAN LONDON, Oncology Report Digital Network |
Major Finding: Overall, 3.2% of patients were found to have pancreatic ductal adenocarcinoma in a region of the gland separate from the intraductal papillary mucinous neoplasm that was under surveillance.
Data Source: Data were taken from a retrospective cohort study of 158 patients who had radiographic surveillance for at least 6 months after diagnosis of an intraductal papillary mucinous neoplasm.
Disclosures: Dr. LaFemina and Dr. Posner disclosed that they had no relevant conflicts of interest.
SAN FRANCISCO – A small proportion of patients with a lower-risk intraductal papillary mucinous neoplasm go on to develop pancreatic ductal adenocarcinoma in an entirely separate region of the gland, an outcome that raises questions about the surveillance strategy for these patients.
Dr. Jennifer LaFemina and her colleagues at the Memorial Sloan-Kettering Cancer Center, New York, retrospectively examined data for 158 patients who were seen at the center in 1989-2010 and who had intraductal papillary mucinous neoplasms (IPMNs) with favorable enough initial features that they were followed with radiographic surveillance for at least 6 months after diagnosis, instead of being taken right to surgery.
Five patients (3.2%) developed pancreatic cancer in a different part of the gland, she reported at a meeting on gastrointestinal cancers sponsored by the American Society of Clinical Oncology. In all cases, the cancer was stage 2A or 2B at diagnosis and was resected with negative margins; however, with a median follow-up of just 1 year, three of the five patients have died.
Dr. LaFemina noted that several published studies have shown that IPMN represents a field defect of ductal instability, and although many have focused on the risk of developing malignancy in the IPMN cyst itself, "the risk of developing a cancer in a region of the pancreas separate from the target cyst that we are monitoring is poorly defined."
In her study, 97 of the 158 patients eventually underwent resection at a median of 16 months after IPMN diagnosis because of a worrisome change either in the IPMN target cyst or elsewhere in the pancreas (J. Clin. Oncol. 2012;30 [suppl 4]:abstract 152). "Five patients ultimately came to surgery not because of the target cyst but because of a ductal adenocarcinoma without IPMN that developed while we were watching them," Dr. LaFemina explained. (In all, 13 of the patients having resection were found to have cancer at the IPMN target cyst.)
In four of these five cases of a separate cancer, the IPMN that had been under surveillance was of the branched-duct subtype and was smaller, measuring no more than 1.6 cm. And in three cases, the time from diagnosis of the IPMN to diagnosis of the separate cancer was fairly short, just 16 months or less.
"Diagnostic, operative, and surveillance strategies should consider the cancer risk not only to the [IPMN] target cyst that we are presented with, but also to the entire gland," Dr. LaFemina recommended. Although the center has not changed its surveillance strategy for these patients, she said that this new information raises some concerns.
The findings also bring up the question of whether to recommend total pancreatectomy for patients who undergo resection, to be on the safe side. "At this point, we are not endorsing total pancreatectomy for a number of reasons," she said – notably because of the difficulty of predicting preoperatively what is actually going on in the gland.
A key question is to determine what is different about patients who develop an adenocarcinoma separate from the IPMN. "Can we identify them and watch them [more closely]? We don’t have that answer yet," Dr. LaFemina noted.
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