review of literature on clinical pancreatology - The Pancreapedia
review of literature on clinical pancreatology - The Pancreapedia
review of literature on clinical pancreatology - The Pancreapedia
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interval 0.80 to 0.96]. On subgroup analysis, <strong>on</strong>ly stage IIB (T1-3N1) patients enjoyed astatistically significant benefit associated with radiotherapy (hazaed ratio, 0.70; 95 %c<strong>on</strong>fidence interval 0.62 to 0.79). Although radiotherapy is associated with a survival benefitfor n<strong>on</strong>metastatic patients as a whole, this trend appears to predominantly derive from asurvival benefit in patients with stage IIB disease [532].Adjuvants am<strong>on</strong>g elderlyIt was c<strong>on</strong>ducted a populati<strong>on</strong>-based study to describe the utilizati<strong>on</strong>, determinants, andsurvival effects <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant therapies after surgery am<strong>on</strong>g older patients with pancreaticcancer. Using Surveillance, Epidemiology, and End Results-Medicare data, it was identifiedpatients older than 65 years who received surgical resecti<strong>on</strong> for pancreatic cancer during1992-2002. Approximately 49 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> patients received adjuvant therapy after surgery.Patient factors associated with increased receipt <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant therapy included more recentdiagnosis, younger age, stage II disease, higher income, and geographic locati<strong>on</strong>. Hospitalfactors associated with increased receipt <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant therapy included cooperative groupmembership and larger size. Adjuvant treatments associated with a significant reducti<strong>on</strong> in 2-year mortality (relative to surgery al<strong>on</strong>e) were chemoradiati<strong>on</strong> or radiati<strong>on</strong> al<strong>on</strong>e but notchemotherapy al<strong>on</strong>e. <strong>The</strong> findings suggest that adjuvant chemoradiati<strong>on</strong> and, to a lesserdegree, radiati<strong>on</strong> <strong>on</strong>ly are associated with a reducti<strong>on</strong> in the risk <str<strong>on</strong>g>of</str<strong>on</strong>g> mortality am<strong>on</strong>g olderpatients who undergo surgery for pancreatic cancer. However, receipt <str<strong>on</strong>g>of</str<strong>on</strong>g> adjuvant therapyvaried by period and geography as well as by certain patient and hospital factors [533].Palliative cytotoxic treatmentEvaluati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> effectsA study was c<strong>on</strong>ducted to assess changes in tumor vascularity using c<strong>on</strong>trast-enhancedultras<strong>on</strong>ography in patients with pancreatic carcinoma under systemic chemotherapy and toexamine the correlati<strong>on</strong> am<strong>on</strong>g vascular change, clinicopathologic factors, and outcome.Forty-<strong>on</strong>e c<strong>on</strong>secutive patients with histopathologically c<strong>on</strong>firmed pancreatic carcinoma whohad distant metastases and were under systemic chemotherapy were recruited. C<strong>on</strong>trastenhancedultras<strong>on</strong>ography was performed before and after 1 and 2 cycles <str<strong>on</strong>g>of</str<strong>on</strong>g> treatment.<strong>The</strong>vascular signals from the tumor were c<strong>on</strong>tinuously recorded,and the highest signal intensitywas selected and classified into 5 categories by their intensity. As for the tumor resp<strong>on</strong>sedetermined by dynamic computed tomography after 2 cycles, 6 patients showed a partialresp<strong>on</strong>se, 25 remained stable, and in 10 patients, the disease progressed. A significantrelati<strong>on</strong>ship was observed between vascular change after 1 cycle and tumor resp<strong>on</strong>se.Progressi<strong>on</strong>-free survival and overall survival were significantly short in the case <str<strong>on</strong>g>of</str<strong>on</strong>g> patientsshowing increased vascularity after 1 and 2 cycles <str<strong>on</strong>g>of</str<strong>on</strong>g> chemotherapy, compared with thosewho did not. It was c<strong>on</strong>cluded that c<strong>on</strong>trast-enhanced ultras<strong>on</strong>ography was useful toevaluate tumor vascular changes and thereby the effect <str<strong>on</strong>g>of</str<strong>on</strong>g> systemic chemotherapy, as wellas the prognosis <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with advanced pancreatic carcinoma [534].GemcitabineGemcitabine is an anti-cancer drug known to be safe and effective for pancreatic or biliarytract cancers, but lung injury is also known to be a rare side effect that sometimes becomessevere. It was report seven cases <str<strong>on</strong>g>of</str<strong>on</strong>g> lung injury during gemcitabine treatment. Drug-inducedlung injury was suspected in all cases. <strong>The</strong> male : female ratio was 5:2, and the averagepatient age was 71. Four had pancreatic cancers and three had biliary tract cancers.Gemcitabine had been administered an average 5.9 times at a dose <str<strong>on</strong>g>of</str<strong>on</strong>g> 1141 mg. Patientsshowed a diffuse or patchy shadow mainly in the lower lung <strong>on</strong> computed tomographyexaminati<strong>on</strong>. Grades <str<strong>on</strong>g>of</str<strong>on</strong>g> adverse events were greater than 3 in all cases. Three patients died<str<strong>on</strong>g>of</str<strong>on</strong>g> the lung injury. Five cases had pulm<strong>on</strong>ary emphysema, 2 had metastatic lung tumor asunderlying pulm<strong>on</strong>ary lesi<strong>on</strong>s, and these were assumed to have been important risk factorsfor drug-induced interstitial lung injury during gemcitabine treatment [535].