TY - JOUR
T1 - Prognostic value of serial blood S100B determinations in stage IIB-III melanoma patients
T2 - A corollary study to EORTC trial 18952
AU - Bouwhuis, M. G.
AU - Suciu, S.
AU - Kruit, W.
AU - Sals, F.
AU - Stoitchkov, K.
AU - Patel, P.
AU - Cocquyt, V.
AU - Thomas, J.
AU - Liénard, D.
AU - Eggermont, A. M.M.
AU - Ghanem, G.
N1 - Funding Information:
Supported in part by grants from the National Cancer Institute (grant numbers 2U10-CA11488-26 through 5U10-CA11488-39), by a donation from the EORTC Charitable Trust and by Sangtec Medical, Sweden. Its contents are solely the responsibility of the authors and do not represent the official views of the National Cancer Institute (Bethesda, Maryland, USA).
PY - 2011/2
Y1 - 2011/2
N2 - S100B is a prognostic factor for melanoma as elevated levels correlate with disease progression and poor outcome. We determined its prognostic value based on updated information using serial determinations in stage IIb/III melanoma patients. 211 Patients who participated in the EORTC 18952 trial, evaluating efficacy of adjuvant intermediate doses of interferon α2b (IFN) versus observation, entered a corollary study. Over a period of 36 months, 918 serum samples were collected. The Cox time-dependent model was used to assess prognostic value of the latest (most recent) S100B determination. At first measurement, 178 patients had S100B values <0.2 μg/l and 33 ≥ 0.2 μg/l. Within the first group, 61 patients had, later on, an increased value of S100B (≥0.2 μg/l). An initial increased value of S100B, or during follow-up, was associated with worse distant metastasis-free survival (DMFS); hazard ratio (HR) of S100B ≥ 0.2 versus S100B < 0.2 was 5.57 (95% confidence interval (CI) 3.81-8.16), P < 0.0001, after adjustment for stage, number of lymph nodes and sex. In stage IIb patients, the HR adjusted for sex was 2.14 (95% CI 0.71, 6.42), whereas in stage III, the HR adjusted for stage, number of lymph nodes and sex was 6.76 (95% CI 4.50-10.16). Similar results were observed regarding overall survival (OS). Serial determination of S100B in stage IIb-III melanoma is a strong independent prognostic marker, even stronger compared to stage and number of positive lymph nodes. The prognostic impact of S100B ≥ 0.2 μg/l is more pronounced in stage III disease compared with stage IIb.
AB - S100B is a prognostic factor for melanoma as elevated levels correlate with disease progression and poor outcome. We determined its prognostic value based on updated information using serial determinations in stage IIb/III melanoma patients. 211 Patients who participated in the EORTC 18952 trial, evaluating efficacy of adjuvant intermediate doses of interferon α2b (IFN) versus observation, entered a corollary study. Over a period of 36 months, 918 serum samples were collected. The Cox time-dependent model was used to assess prognostic value of the latest (most recent) S100B determination. At first measurement, 178 patients had S100B values <0.2 μg/l and 33 ≥ 0.2 μg/l. Within the first group, 61 patients had, later on, an increased value of S100B (≥0.2 μg/l). An initial increased value of S100B, or during follow-up, was associated with worse distant metastasis-free survival (DMFS); hazard ratio (HR) of S100B ≥ 0.2 versus S100B < 0.2 was 5.57 (95% confidence interval (CI) 3.81-8.16), P < 0.0001, after adjustment for stage, number of lymph nodes and sex. In stage IIb patients, the HR adjusted for sex was 2.14 (95% CI 0.71, 6.42), whereas in stage III, the HR adjusted for stage, number of lymph nodes and sex was 6.76 (95% CI 4.50-10.16). Similar results were observed regarding overall survival (OS). Serial determination of S100B in stage IIb-III melanoma is a strong independent prognostic marker, even stronger compared to stage and number of positive lymph nodes. The prognostic impact of S100B ≥ 0.2 μg/l is more pronounced in stage III disease compared with stage IIb.
KW - Adjuvant therapy
KW - Interferon α-2b
KW - Melanoma
KW - Prognostic marker
KW - RCT
KW - S100B
UR - http://www.scopus.com/inward/record.url?scp=79251599240&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2010.10.005
DO - 10.1016/j.ejca.2010.10.005
M3 - Article
AN - SCOPUS:79251599240
SN - 0959-8049
VL - 47
SP - 361
EP - 368
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 3
ER -