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癌症患者在进行细胞抑制药物治疗前后的结核菌素和二硝基氯苯(DNCB)试验。

Tuberculin and dinitrochlorobenzene (DNCB) tests in cancer patients before and after cytostatic drug therapy.

作者信息

Weber W, Missmahl H P, Mazloumi B

出版信息

Klin Wochenschr. 1978 Sep 15;56(18):905-9. doi: 10.1007/BF01489216.

Abstract

In 137 patients with different kinds of cancer and different cancer stage, cell-mediated immunity was investigated by DNCB (dinitrochlorobenzene) and tuberculin test. These two skin tests were performed before and after cytostatic drug combination therapy. For a collective of cancer patients we found a positive correlation between skin reactions and prognosis and a negative correlation between skin reactions and cancer stage. After cytostatic drug therapy skin reactions could be significantly stronger. This could be observed in 50% when one test was positive before chemotherapy and in only 20% when both tests were negative before chemotherapy. There existed a significant correlation between an increased reaction after cytostatic drug therapy and objective tumor regression. When skin reactions decreased, tumor progression was seen in all cases. Due to these observations we use skin reactions as a good parameter for therapy results. When delayed cutaneous hypersensitivity impairs 2--3 weeks after chemotherapy, we then change the cytostatic drug combination immediately. We cannot say at this moment, whether an improvement of cytostatic drug therapy can be reached in this way.

摘要

对137例患有不同类型癌症及处于不同癌症阶段的患者,通过二硝基氯苯(DNCB)和结核菌素试验研究细胞介导免疫。这两项皮肤试验在细胞毒性药物联合治疗前后进行。对于一组癌症患者,我们发现皮肤反应与预后呈正相关,与癌症阶段呈负相关。细胞毒性药物治疗后,皮肤反应可能显著增强。化疗前一项试验呈阳性时,50%的患者会出现这种情况;化疗前两项试验均呈阴性时,只有20%的患者会出现这种情况。细胞毒性药物治疗后反应增强与肿瘤客观消退之间存在显著相关性。当皮肤反应减弱时,所有病例均出现肿瘤进展。基于这些观察结果,我们将皮肤反应作为治疗效果的良好参数。当化疗后延迟性皮肤超敏反应在2至3周后受损时,我们会立即改变细胞毒性药物组合。目前我们尚不能确定通过这种方式是否能改善细胞毒性药物治疗效果。

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