TY - JOUR
T1 - Results of interleukin-2-based treatment in advanced melanoma
T2 - A case record-based analysis of 631 patients
AU - Keilholz, Ulrich
AU - Conradt, Christian
AU - Legha, Sewa S.
AU - Khayat, David
AU - Scheibenbogen, Carmen
AU - Thatcher, Nick
AU - Goey, Swan Hoo
AU - Gore, Martin
AU - Dorval, Thierry
AU - Hancock, Barry
AU - Punt, Cornelis J.A.
AU - Dummer, Reinhard
AU - Avril, Marie Francoise
AU - Bröcker, Eva B.
AU - Benhammouda, A.
AU - Eggermont, Alexander M.M.
AU - Pritsch, Maria
PY - 1998/9
Y1 - 1998/9
N2 - Purpose: In patients with stage IV melanoma, durable responses have been reported with treatment regimens that involve high-dose interleukin-2 (IL- 2). We analyze long-term results of 631 melanoma patients from 12 institutions who had received IL-2 alone, in combination with interferon alfa 2a or 2b (IFNα), or with cytotoxic drugs. Methods: Case records that contained pretreatment parameters, response data, and updated survival information were collected. After univariate analysis, the multivariate evaluation of the impact of pretreatment parameters on response and survival was performed by logistic regression and Cox's regression, respectively. Results: Patients were divided into four groups according to treatment: IL-2 alone (n = 117), IL-2 and chemotherapy (n = 49), IL-2 and IFNα (n = 153), and IL-2, chemotherapy, and IFNα (n = 312). The median survival of all patients was 10.5 months and the 2- and 5-year survival rates were 19.9% and 10.4%, respectively. Independent prognostic factors for response and survival were entirely different, treatment group being the only significant factor for response, and serum lactate dehydrogenase (LDH), metastatic site, and performance predicting survival. The addition of IFNα to IL-2 was associated with prolonged survival, but the effect of additional chemotherapy was less obvious. Conclusion: Serum LDH, metastatic site, and performance status are useful stratification factors for randomized trials in metastatic melanoma. The improved longterm survival rates observed in melanoma patients treated with IL-2/IFNα-containing regimens are notable in contrast to the reported 5-year survival rates of 2% to 6% achieved with chemotherapy, but because selection bias cannot be ruled out, the impact of IL-2, as well as all other components of the treatment regimens, on survival needs to be confirmed in prospective randomized trials.
AB - Purpose: In patients with stage IV melanoma, durable responses have been reported with treatment regimens that involve high-dose interleukin-2 (IL- 2). We analyze long-term results of 631 melanoma patients from 12 institutions who had received IL-2 alone, in combination with interferon alfa 2a or 2b (IFNα), or with cytotoxic drugs. Methods: Case records that contained pretreatment parameters, response data, and updated survival information were collected. After univariate analysis, the multivariate evaluation of the impact of pretreatment parameters on response and survival was performed by logistic regression and Cox's regression, respectively. Results: Patients were divided into four groups according to treatment: IL-2 alone (n = 117), IL-2 and chemotherapy (n = 49), IL-2 and IFNα (n = 153), and IL-2, chemotherapy, and IFNα (n = 312). The median survival of all patients was 10.5 months and the 2- and 5-year survival rates were 19.9% and 10.4%, respectively. Independent prognostic factors for response and survival were entirely different, treatment group being the only significant factor for response, and serum lactate dehydrogenase (LDH), metastatic site, and performance predicting survival. The addition of IFNα to IL-2 was associated with prolonged survival, but the effect of additional chemotherapy was less obvious. Conclusion: Serum LDH, metastatic site, and performance status are useful stratification factors for randomized trials in metastatic melanoma. The improved longterm survival rates observed in melanoma patients treated with IL-2/IFNα-containing regimens are notable in contrast to the reported 5-year survival rates of 2% to 6% achieved with chemotherapy, but because selection bias cannot be ruled out, the impact of IL-2, as well as all other components of the treatment regimens, on survival needs to be confirmed in prospective randomized trials.
UR - http://www.scopus.com/inward/record.url?scp=0031718717&partnerID=8YFLogxK
U2 - 10.1200/JCO.1998.16.9.2921
DO - 10.1200/JCO.1998.16.9.2921
M3 - Article
AN - SCOPUS:0031718717
SN - 0732-183X
VL - 16
SP - 2921
EP - 2929
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 9
ER -