PMID- 19214504 OWN - NLM STAT- MEDLINE DCOM- 20090813 LR - 20240426 IS - 1432-0851 (Electronic) IS - 0340-7004 (Print) IS - 0340-7004 (Linking) VI - 58 IP - 10 DP - 2009 Oct TI - The common Scandinavian human leucocyte antigen ancestral haplotype 62.1 as prognostic factor in patients with advanced malignant melanoma. PG - 1599-608 LID - 10.1007/s00262-009-0669-8 [doi] AB - PURPOSE: We have previously demonstrated an association of the human leukocyte antigen (HLA), HLA-A2 allele with ovarian and prostate cancer mortality as well as a segregation of the ancestral HLA haplotype (AHH) 62.1 [(A2) B15 Cw3 DRB1*04] in patients with stage III-IV serous ovarian cancer. The objective of the present study was to determine the role of the HLA phenotype on the prognosis in stage III-IV malignant melanoma patients. PATIENTS AND METHODS: A cohort of metastatic malignant melanoma patients (n = 91), in stage III (n = 26) or IV (n = 65) were analysed for HLA-A, -B, -Cw and -DRB1 types by PCR/sequence-specific primer method. The frequencies of HLA alleles in the patients were compared to that of healthy Swedish bone marrow donors. The effect of HLA types on prognosis was defined by Kaplan-Meier and Cox analysis. RESULTS: The presence of the AHH 62.1 in clinical stage IV patients was significantly and independently associated with the worst survival rate recorded from the appearance of metastasis (HR = 2.14; CI = 1.02-4.4; P = 0.04). In contrast, the period from the primary diagnosis to metastasis was the longest in patients with this haplotype (HR = 0.40; CI = 0.17-0.90; P = 0.02). CONCLUSIONS: Melanoma patients in our cohort with 62.1 AHH which is associated with autoimmune diseases have an initial strong anti-tumour control with longer metastasis-free period. These patients have rapid progression after the appearance of metastasis, responding poorly to chemo- or/and immunotherapy. This apparently paradoxical clinical process could be due to the interplay between tumour clones escape and immune surveillance ending up with a rapid disease progression. FAU - Helgadottir, Hildur AU - Helgadottir H AD - Department of Oncology-Pathology, Karolinska Institute, Radiumhemmet, Karolinska University Hospital, 171 76, Stockholm, Sweden. FAU - Andersson, Emilia AU - Andersson E FAU - Villabona, Lisa AU - Villabona L FAU - Kanter, Lena AU - Kanter L FAU - van der Zanden, Henk AU - van der Zanden H FAU - Haasnoot, Geert W AU - Haasnoot GW FAU - Seliger, Barbara AU - Seliger B FAU - Bergfeldt, Kjell AU - Bergfeldt K FAU - Hansson, Johan AU - Hansson J FAU - Ragnarsson-Olding, Boel AU - Ragnarsson-Olding B FAU - Kiessling, Rolf AU - Kiessling R FAU - Masucci, Giuseppe Valentino AU - Masucci GV LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090213 PL - Germany TA - Cancer Immunol Immunother JT - Cancer immunology, immunotherapy : CII JID - 8605732 RN - 0 (Biomarkers, Tumor) RN - 0 (HLA-A Antigens) RN - 0 (HLA-B Antigens) RN - 0 (HLA-C Antigens) RN - 0 (HLA-Cw1 antigen) RN - 0 (HLA-DR Antigens) RN - 0 (HLA-DRB1 Chains) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Biomarkers, Tumor/genetics MH - Cohort Studies MH - Female MH - HLA-A Antigens/*genetics MH - HLA-B Antigens/*genetics MH - HLA-C Antigens/*genetics MH - HLA-DR Antigens/*genetics MH - HLA-DRB1 Chains MH - Haplotypes/*genetics MH - Humans MH - Male MH - Melanoma/*genetics/mortality MH - Middle Aged MH - Neoplasm Staging MH - Polymerase Chain Reaction MH - Prognosis MH - Survival Rate PMC - PMC11030936 EDAT- 2009/02/14 09:00 MHDA- 2009/08/14 09:00 PMCR- 2009/02/13 CRDT- 2009/02/14 09:00 PHST- 2008/12/01 00:00 [received] PHST- 2009/01/21 00:00 [accepted] PHST- 2009/02/14 09:00 [entrez] PHST- 2009/02/14 09:00 [pubmed] PHST- 2009/08/14 09:00 [medline] PHST- 2009/02/13 00:00 [pmc-release] AID - 669 [pii] AID - 10.1007/s00262-009-0669-8 [doi] PST - ppublish SO - Cancer Immunol Immunother. 2009 Oct;58(10):1599-608. doi: 10.1007/s00262-009-0669-8. Epub 2009 Feb 13.