PMID- 8756369 OWN - NLM STAT- MEDLINE DCOM- 19960913 LR - 20111117 IS - 0008-543X (Print) IS - 0008-543X (Linking) VI - 78 IP - 4 DP - 1996 Aug 15 TI - Malignant melanoma: relationship of the human leukocyte antigen class II gene DQB1*0301 to disease recurrence in American Joint Committee on Cancer Stage I or II. PG - 758-63 AB - BACKGROUND: Melanoma patients who carry the human leukocyte antigen (HLA) Class II allele DQB1*0301 have an increased frequency of metastases at presentation compared with those lacking HLA-DQB1*0301. This study was designed to determine whether HLA-DQB1*0301 is associated with an increased risk of recurrence in melanoma patients presenting with American Joint Committee on Cancer (AJCC) Stage I or II (localized) disease. METHODS: Molecular oligotyping of HLA-DQ genes was performed for 259 patients with AJCC Stage I or II melanoma. Rate of disease recurrence was determined by retrospective review and prospective follow-up. Kaplan-Meier analysis, log rank, and proportional hazard (Cox) comparison were performed. RESULTS: Median follow-up was 24 months. Minimum follow-up was 6 months. Although HLA-DQB1*0301-positive and -negative patients were balanced with regard to standard melanoma prognostic factors (primary tumor thickness, level of invasion, presence of ulceration, anatomic location, and sex), HLA-DQB1*0301-positive patients were more likely to develop locally recurrent, regional, or distant metastatic melanoma during follow-up (actuarial median disease free survival 48 months [DQB1*0301-positive patients] vs. 97 months [DQB1*0301-negative patients]; log rank P = 0.0002). HLA-DQB1*0301 status, in addition to primary tumor thickness, was an independent prognostic indicator in these patients (Cox multivariate P = 0.02). CONCLUSIONS: Patients presenting with localized melanoma who carry HLA-DQB1*0301 are at an increased risk of developing recurrent disease compared with stage-matched patients who lack this allele. HLA-DQB1*0301 is a genomic marker which independently identifies melanoma patients in whom recurrence is more likely, and is potentially useful in selecting those most likely to benefit from adjuvant therapy. FAU - Lee, J E AU - Lee JE AD - Department of Surgical Oncology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA. FAU - Lu, M AU - Lu M FAU - Mansfield, P F AU - Mansfield PF FAU - Platsoucas, C D AU - Platsoucas CD FAU - Reveille, J D AU - Reveille JD FAU - Ross, M I AU - Ross MI LA - eng GR - CA16672/CA/NCI NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Cancer JT - Cancer JID - 0374236 RN - 0 (HLA-DQ Antigens) RN - 0 (HLA-DQ beta-Chains) RN - 0 (HLA-DQB1 antigen) SB - IM MH - Alleles MH - Female MH - Follow-Up Studies MH - HLA-DQ Antigens/*genetics MH - HLA-DQ beta-Chains MH - Humans MH - Lymphatic Metastasis MH - Male MH - Melanoma/*genetics/pathology MH - Middle Aged MH - Neoplasm Recurrence, Local/*genetics/pathology MH - Neoplasm Staging MH - Predictive Value of Tests MH - Prognosis EDAT- 1996/08/15 00:00 MHDA- 2000/06/20 09:00 CRDT- 1996/08/15 00:00 PHST- 1996/08/15 00:00 [pubmed] PHST- 2000/06/20 09:00 [medline] PHST- 1996/08/15 00:00 [entrez] AID - 10.1002/(SICI)1097-0142(19960815)78:4<758::AID-CNCR11>3.0.CO;2-U [pii] AID - 10.1002/(SICI)1097-0142(19960815)78:4<758::AID-CNCR11>3.0.CO;2-U [doi] PST - ppublish SO - Cancer. 1996 Aug 15;78(4):758-63. doi: 10.1002/(SICI)1097-0142(19960815)78:4<758::AID-CNCR11>3.0.CO;2-U.