Table 1 |
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Patient characteristics, treatment and outcomes |
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Case 1 |
Case 2 |
Case 3 |
Case 4 |
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Age |
64 |
70 |
56 |
61 |
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Sex |
Male |
Male |
Male |
Male |
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Presenting Symptoms |
Abdominal pain, nausea, weight loss then jaundice |
Vomiting, weight loss |
Dyspepsia, weight loss |
Abdominal pain, weight loss then jaundice |
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Delay until diagnosis |
5 weeks |
3 months |
18 months |
4 months |
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Method of diagnosis |
Endoscopic ultrasound FNA |
Laparotomy |
Laparotomy |
Laparotomy |
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CT appearance |
6 cm pancreatic mass with biliary obstruction and portal vein involvement |
Large peri-pancreatic mass |
5 cm pancreatic mass |
Pancreatic mass and peripancreatic lymph nodes |
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Ca-19.9 level* |
500 kU/L |
50 kU/L |
Not available |
39 kU/L |
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Pre-treatment LDH |
Normal |
Elevated |
Normal |
Elevated |
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Histology** |
DLBCL |
DLBCL |
Grade II follicular non-Hodgkins lymphoma |
DLBCL |
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Stage*** |
IIE |
IIE |
IIE |
IIE |
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Prognostic index |
Low-intermediate risk (IPI 2/5) |
Low-intermediate risk (IPI 2/5) |
Low risk (FLIPI 1/5) |
Low-intermediate risk (IPI 2/5) |
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Treatment |
R-CHOP * 4 then involved-field RT |
CHOP * 3 then involved-field RT |
Involved-field RT then CVP then rituximab |
3 * CHOP then involved-field RT |
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Outcome |
NED at 23 months |
Local recurrence at 32 months post-diagnosis, with poor tolerance of 2nd line chemotherapy and rapid treatment-related death |
NED at 25 months |
Out of field recurrence at 21 months post diagnosis. Salvage chemotherapy and autologous SCT. NED at 64 months from diagnosis |
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CHOP – Cyclophosphamide, doxorubicin, vincristine, prednisone CVP – Cyclophosphamide, vincristine, prednisone DLBCL – diffuse large B-cell non-Hodgkin's lymphoma FLIPI – Follicular lymphoma international prognostic index [8] IPI – International Prognostic Index for the Aggressive Non-Hodgkin's Lymphomas [7] NED – No evidence of disease R-CHOP – Rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone RT – Radiotherapy SCT – Stem cell transplantation * Normal Range 0–50 kU/L ** Histology defined according to REAL classification.[5] *** Staging defined according to Ann Arbor staging system.[4] |
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Grimison et al. BMC Cancer 2006 6:117 doi:10.1186/1471-2407-6-117 |
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