Kradin R L, Kurnick J T, Lazarus D S, Preffer F I, Dubinett S M, Pinto C E, Gifford J, Davidson E, Grove B, Callahan R J
Department of Pathology, Massachusetts General Hospital, Boston.
Lancet. 1989 Mar 18;1(8638):577-80. doi: 10.1016/s0140-6736(89)91609-7.
Tumour-infiltrating lymphocytes (TIL) were isolated and expanded from small tumour biopsy samples of twenty-eight patients (thirteen with malignant melanoma, seven with renal cell carcinoma, and eight with non-small-cell lung cancer). The patients were treated with autologous expanded TIL (about 10(10)) and continuous infusions of recombinant human interleukin-2(1-3 x 10(6) U/m2 per 24 h). 29% of the patients with renal cell cancer and 23% of those with melanoma achieved objective tumour responses lasting 3-14 months. Toxic side-effects were limited, and no patient required intensive-care monitoring. Adoptive immunotherapy with TIL and interleukin-2 may be an effective systemic approach to the treatment of some patients with malignant melanoma and renal cell carcinoma.
从28例患者的小肿瘤活检样本中分离并扩增肿瘤浸润淋巴细胞(TIL)(13例恶性黑色素瘤患者、7例肾细胞癌患者和8例非小细胞肺癌患者)。患者接受自体扩增的TIL(约10¹⁰)治疗,并持续输注重组人白细胞介素-2(每24小时1 - 3×10⁶U/m²)。29%的肾细胞癌患者和23%的黑色素瘤患者获得了持续3 - 14个月的客观肿瘤反应。毒性副作用有限,没有患者需要重症监护监测。TIL和白细胞介素-2的过继性免疫疗法可能是治疗某些恶性黑色素瘤和肾细胞癌患者的一种有效的全身治疗方法。