Scalzo S, Gengaro A, Boccoli G, Masciulli R, Giannella G, Salvo G, Marolla P, Carlini P, Massimini G, Holdener E E
Department of Hematology-Oncology, Instituto Superiore di Sanità, Rome, Italy.
Eur J Cancer. 1990;26(11-12):1152-6. doi: 10.1016/0277-5379(90)90275-x.
Four patients out of twenty with renal cancer and melanoma undergoing cancer immunotherapy with interleukin 2 (IL-2) and interferon alpha-2 (IFN-alpha 2) had laboratory evidence of hypothyroidism starting at cycle three to six, with a decline in serum thyroxine below normal and, in three cases, a rise in serum thyrotropin and thyroglobulin. One hypothyroid patient had elevated serum antimicrosomal antibody titres before the start of treatment and two others responded similarly during therapy. Three of the sixteen euthyroid patients also developed elevated titres of this antibody. Partial or complete remission was observed in seven of the patients--three of the four with hypothyroidism showed tumour regression. Thus IL-2 and IFN-alpha 2 can cause hypothyroidism, presumably via induction or exacerbation of autoimmune thyroid reactions. The occurrence of hypothyroidism may be mediated by high-dose IL-2 (rather than by LAK cell therapy as previously suggested) and potentiated by IFN-alpha 2.
20例接受白细胞介素2(IL-2)和α-2干扰素(IFN-α2)癌症免疫治疗的肾癌和黑色素瘤患者中,有4例在第3至6周期开始出现甲状腺功能减退的实验室证据,血清甲状腺素降至正常水平以下,3例血清促甲状腺素和甲状腺球蛋白升高。1例甲状腺功能减退患者在治疗开始前血清抗微粒体抗体滴度升高,另外2例在治疗期间也有类似反应。16例甲状腺功能正常的患者中有3例该抗体滴度也升高。7例患者出现部分或完全缓解,4例甲状腺功能减退患者中有3例肿瘤消退。因此,IL-2和IFN-α2可能通过诱导或加剧自身免疫性甲状腺反应导致甲状腺功能减退。甲状腺功能减退的发生可能由高剂量IL-2介导(而非如先前认为的由LAK细胞疗法介导),并由IFN-α2增强。