Visco C, Medeiros L J, Jones D, Smith T, Rodriguez M A, McLaughlin P, Romaguera J, Cabanillas F, Sarris A H
Department of Lymphoma and Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Ann Oncol. 2002 Aug;13(8):1290-9. doi: 10.1093/annonc/mdf206.
The aim of this study was to explore the association between extent of cutaneous involvement, presenting features and progression-free survival (PFS) in patients with primary cutaneous non-Hodgkin's lymphoma (PCNHL) of aggressive histology.
Previously untreated patients with localized or extensive PCNHL of aggressive histology, treated with combination chemotherapy, but excluding lymphoblastic lymphoma and mycosis fungoides and its variants, were reviewed retrospectively.
We identified 53 patients, of whom 52 (35 males, 17 females) were treated with doxorubicin-based regimens. Median age was 52 years (range 25-81 years), and disease was localized and extensive in 37 and 16 patients, respectively. Twenty-four patients had diffuse large B-cell lymphoma, nine had grade 3 follicular lymphoma, 13 had peripheral T-cell lymphoma (PTCL; not otherwise specified) and seven had anaplastic large cell lymphoma (WHO classification). With a median follow-up of 101 months (range 2-237 months) for survivors, the 10-year PFS was 65 +/- 7% and overall survival was 72 +/- 8%. The first failure involved the skin in 33% of B-cell and 91% of relapsing T-cell lymphomas. Univariate analysis revealed that PTCL (P = 0.005), lymphopenia (P = 0.01) and high serum levels of beta(2)-microglobulin (P = 0.0006) and LDH (P = 0.002), but not extent of skin involvement, were associated with inferior PFS. Multivariate analysis revealed that only PTCL and high serum lactate dehydrogenase (LDH) were independently associated with inferior PFS.
PTCL and elevated serum LDH level, but not extent of cutaneous involvement are associated with inferior PFS in aggressive PCNHL treated with combination chemotherapy.
本研究旨在探讨侵袭性组织学类型的原发性皮肤非霍奇金淋巴瘤(PCNHL)患者皮肤受累范围、临床表现与无进展生存期(PFS)之间的关联。
回顾性分析既往未经治疗、组织学类型为侵袭性的局限性或广泛性PCNHL患者,这些患者接受联合化疗,但不包括淋巴母细胞淋巴瘤和蕈样肉芽肿及其变异型。
我们共纳入53例患者,其中52例(35例男性,17例女性)接受了含阿霉素的化疗方案。中位年龄为52岁(范围25 - 81岁),疾病局限型和广泛型分别为37例和16例。24例为弥漫性大B细胞淋巴瘤,9例为3级滤泡性淋巴瘤,13例为外周T细胞淋巴瘤(PTCL;未另行分类),7例为间变性大细胞淋巴瘤(世界卫生组织分类)。存活患者的中位随访时间为101个月(范围2 - 237个月),10年PFS为65±7%,总生存期为72±8%。33%的B细胞淋巴瘤和91%复发的T细胞淋巴瘤首次复发累及皮肤。单因素分析显示,PTCL(P = 0.005)、淋巴细胞减少(P = 0.01)、血清β2微球蛋白水平升高(P = 0.0006)和乳酸脱氢酶(LDH)水平升高(P = 0.002)与较差的PFS相关,但皮肤受累范围与PFS无关。多因素分析显示,只有PTCL和血清乳酸脱氢酶(LDH)水平升高与较差的PFS独立相关。
在接受联合化疗的侵袭性PCNHL中,PTCL和血清LDH水平升高与较差的PFS相关,而皮肤受累范围与PFS无关。