Y. Masai et al., ANTICANCER CHEMOSENSITIVITY PROFILE OF FRESHLY SEPARATED HUMAN PANCREATIC-CANCER CELLS ASSESSED BY DNA-SYNTHESIS INHIBITION ASSAY, Journal of surgical oncology, 57(2), 1994, pp. 97-104
The chemosensitivity of 49 freshly separated human pancreatic cancers
to seven kinds of anticancer agents were assessed by a DNA synthesis (
H-3- thymidine incorporation) inhibition assay. DNA synthesis is highe
r in involved lymph nodes (n = 7), malignant effusion (n = 15), liver
metastasis (n = 7), primary cancer (n = 15), and skin metastasis (n =
5). Chemosensitivity assay demonstrates that etoposide, 4-epirubicin,
carboquone, and 5-fluorouracil are more effective than cisplatin, mito
mycin-C, and Adriamycin. In general, metastatic lesions of pancreatic
cancer tend to show higher chemosensitivity than primary lesions. Path
ological analysis demonstrates that small primary pancreatic cancers t
end to be more responsive than large primary cancers, and primary panc
reatic cancers with no regional lymph node involvement also tend to be
more responsive than those with nodal involvement. No significant dif
ferences are seen in terms of tumor spread, vascular involvement, sex
of patient, and histological type. When chemosensitivity assay is not
available, the results df the present study may be beneficial to choos
e the regimens. (C) 1994 Wiley-Liss, Inc.