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125I-labelled human chorionic gonadotrophin (hCG) as an elimination marker in the evaluation of hCG decline during chemotherapy in patients with testicular cancer

机译:125I标记的人绒毛膜促性腺激素(hCG)作为评估睾丸癌患者化疗期间hCG下降的消除标记

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摘要

The rate of reduction in the concentration of serum human chorionic gonadotrophin (hCG) following chemotherapy for germ cell tumours may follow a complex pattern, with longer apparent half-life during later stages of chemotherapy, even in patients treated successfully. The commonly used half-life of less than 3 days for hCG to monitor the effect of chemotherapy in patients with germ cell tumours of the testis may represent too simple a model. 125I-labelled hCG was injected intravenously in 27 patients with germ cell tumours and elevated hCG during chemotherapy. The plasma radioactivity and hCG concentrations were followed. During chemotherapy, the plasma disappearance of hCG showed a biphasic pattern, with an initial fast and a later slow component in all patients. Using the steep part of the hCG plasma disappearance curve, five patients who achieved long-term remission had half-lives longer than 3 days (3.6–6.8 days), whereas four out of five patients not achieving long-term remission had half-lives shorter than 3 days. After the third treatment cycle, eight patients who achieved long-term remission had hCG half-lives longer than 3 days (7.4–17.0 days). In these patients, the plasma disappearance of [125I]hCG was equivalent to that of hCG. Thus, the slow decline of hCG represented a slow plasma disappearance rather than a hCG production from vital tumour cells and could, consequently, not be used to select patients for additional or intensified chemotherapy. The concept of a fixed half-life for plasma hCG during treatment of hCG-producing germ cell tumours is inappropriate and should be revised. Difficulties in interpreting a slow decline of hCG may be overcome by comparing the plasma disappearance of total hCG with the plasma disappearance of [125I]hCG. © 1999 Cancer Research Campaign
机译:对于生殖细胞肿瘤,化疗后血清人绒毛膜促性腺激素(hCG)浓度降低的速率可能遵循复杂的模式,即使在治疗成功的患者中,化疗后阶段的表观半衰期更长。 hCG监测睾丸生殖细胞肿瘤患者化疗效果的常用半衰期少于3天,可能代表了一个过于简单的模型。在化疗期间,经静脉注射 125 I标记的hCG至27例生殖细胞肿瘤和hCG升高的患者。追踪血浆放射性和hCG浓度。在化疗期间,hCG的血浆消失呈双相模式,在所有患者中都有最初的快和慢的成分。使用hCG血浆消失曲线的陡峭部分,获得长期缓解的五名患者的半衰期超过3天(3.6-6.8天),而未达到长期缓解的五分之四的患者具有半衰期少于3天。在第三个治疗周期之后,八位获得长期缓解的患者的hCG半衰期超过3天(7.4-17.0天)。在这些患者中,[ 125 I] hCG的血浆消失与hCG相同。因此,hCG的缓慢下降代表缓慢的血浆消失,而不是重要肿瘤细胞产生的hCG,因此不能用于选择患者进行其他或强化化疗。在产生hCG的生殖细胞肿瘤的治疗过程中,血浆hCG的固定半衰期的概念是不合适的,应予以修订。比较总hCG的血浆消失与[ 125 I] hCG的血浆消失,可以克服解释hCG缓慢下降的困难。 ©1999癌症研究运动

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