TY - JOUR
T1 - Prediction of response to treatment in superficial bladder carcinoma through pattern of interleukin-2 gene expression
AU - Kaempfer, R.
AU - Gerez, L.
AU - Farbstein, H.
AU - Madar, L.
AU - Hirschman, O.
AU - Nussinovich, R.
AU - Shapiro, A.
PY - 1996/6
Y1 - 1996/6
N2 - Purpose: Superficial bladder carcinoma, treated by resection and intravesical administration of bacillus Calmette-Guerin (BCG), yields a remission rate that approaches 70%. We examined whether expression of interleukin-2 (IL-2) or interferon-γ (IFN-γ) genes can serve to predict response. Patients and Methods: During BCG treatment, we analyzed induction of IL-2 and IFN-γ mRNA in peripheral-blood mononuclear cells (PBMC) from 73 patients: 51 with papillary tumors and 22 with carcinoma-in-situ (CIS). Results were correlated with remission, relapse, or tumor persistence over a 4-year follow-up period. Results: Independent of tumor type, induction of IL- 2 mRNA was observed for patients who responded with remission, but not for those who relapsed (P = .0001). Multivariate logistic analysis showed that inducibility of IL-2 mRNA is the discriminating parameter, which yields a predictive value of 97% for remission. Of 23 patients with relapse/persistence, 22 lacked inducibility of IL-2 mRNA (sensitivity, 95.6%), while 35 of 50 patients in remission exhibited inducibility (specificity, 70%). For patients with carcinoma-in-situ, in which remission or failure depends solely on response to BCG, sensitivity and specificity were 88% and 86%, respectively; for patients with papillary tumors, they were 100% and 64%. IFN-γ mRNA, by contrast, was clearly inducible in PBMC from all patients (P = .51). The disease-free interval increased progressively with inducibility of IL-2 mRNA; this trend was highly significant (P = .0001). Conclusion: IL-2 gene expression is essential for mounting an antitumor response in superficial bladder carcinoma. Inducibility of IL-2 mRNA is an independent prognostic parameter and useful predictive indicator of remission versus relapse.
AB - Purpose: Superficial bladder carcinoma, treated by resection and intravesical administration of bacillus Calmette-Guerin (BCG), yields a remission rate that approaches 70%. We examined whether expression of interleukin-2 (IL-2) or interferon-γ (IFN-γ) genes can serve to predict response. Patients and Methods: During BCG treatment, we analyzed induction of IL-2 and IFN-γ mRNA in peripheral-blood mononuclear cells (PBMC) from 73 patients: 51 with papillary tumors and 22 with carcinoma-in-situ (CIS). Results were correlated with remission, relapse, or tumor persistence over a 4-year follow-up period. Results: Independent of tumor type, induction of IL- 2 mRNA was observed for patients who responded with remission, but not for those who relapsed (P = .0001). Multivariate logistic analysis showed that inducibility of IL-2 mRNA is the discriminating parameter, which yields a predictive value of 97% for remission. Of 23 patients with relapse/persistence, 22 lacked inducibility of IL-2 mRNA (sensitivity, 95.6%), while 35 of 50 patients in remission exhibited inducibility (specificity, 70%). For patients with carcinoma-in-situ, in which remission or failure depends solely on response to BCG, sensitivity and specificity were 88% and 86%, respectively; for patients with papillary tumors, they were 100% and 64%. IFN-γ mRNA, by contrast, was clearly inducible in PBMC from all patients (P = .51). The disease-free interval increased progressively with inducibility of IL-2 mRNA; this trend was highly significant (P = .0001). Conclusion: IL-2 gene expression is essential for mounting an antitumor response in superficial bladder carcinoma. Inducibility of IL-2 mRNA is an independent prognostic parameter and useful predictive indicator of remission versus relapse.
UR - http://www.scopus.com/inward/record.url?scp=0029885357&partnerID=8YFLogxK
U2 - 10.1200/JCO.1996.14.6.1778
DO - 10.1200/JCO.1996.14.6.1778
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AN - SCOPUS:0029885357
SN - 0732-183X
VL - 14
SP - 1778
EP - 1786
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 6
ER -