Abstract
4123 Background: Isolated or predominant carcinomatosis is not an uncommon presentation in patients with carcinoma of unknown primary (CUP). Primary peritoneal serous carcinoma (PPSC) is a well studied favorable CUP subset though data on non–PPSC is lacking and this group comprises of a large differential (gastric, colorectal, appendiceal, pancreatico-biliary and other cancer profiles). Information on the clinicopathologic characteristics and survival of these patients can help articulate a management strategy for these patients. Methods: Review of a M. D. Anderson Cancer Center CUP database from 2005 to 2010 has identified 64 patients in an ongoing study. Patients with predominant disease sites other than peritoneum/omentum were excluded. Data on demographics, imaging, detailed pathology, treatment, clinical course and survival was collected. Results: Median age of the patients is 56 years (range 31-86) and 38% are male. 13 (20%) women presented with typical PPSC. Immunohistochemistry (IHC) for all patients included a large range of markers – the most helpful in diagnosis were CK 7 (positive 46/72%), CK 20 (positive 33/51%), CDX-2 (positive 28, 44%), WT-1 (positive 9, 14%) and Calretinin (positive 2, 3%). 43 (67%) patients presented with ascites. First line treatments were grouped into: Colorectal regimens (FOLFOX/FOLFIRI based -30 pts/47%); Pancreaticobiliary regimens (Gemcitabine based - 5 pts/ 8%), taxane+platinum -21 pts/33%); other or no therapy -8 pts/12%. Median overall survival was 25 months (CI 20-30 months; OS not reached for PPSC and 22 months for non-PPSC patients). Conclusions: Uniform and limited IHC including CK 7/20; CDX-2, WT-1 and Calretinin are the most helpful first tier IHC in determining the cancer profile and choosing the best treatment strategy for isolated carcinomatosis CUP patients. Non-PPSC carcinomatosis is not an uncommon CUP presentation and these patients often are candidates for non taxane based therapies. Patients with a GI cancer (CDX-2 positive non-PPSC) IHC profile are good candidates for the colorectal armanentarium of drugs with survival of these patients similar to patients with metastatic colorectal cancer.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have