Ziske C, Schlie C, Gorschlüter M, Glasmacher A, Mey U, Strehl J, Sauerbruch T, Schmidt-Wolf I G H
Medizinische Klinik und Poliklinik I, Rheinische Friedrich-Wilhelms-Universität, Sigmund-Freud-Str. 25, 53105 Bonn, Germany.
Br J Cancer. 2003 Oct 20;89(8):1413-7. doi: 10.1038/sj.bjc.6601263.
Serum carbohydrate antigen 19-9 (CA 19-9) has been identified as a useful tumour marker for diagnosis of exocrine pancreatic carcinoma, but its value for evaluating the response to chemotherapy with gemcitabine is not clear. Tumour regression in pancreatic carcinoma is hard to determine due to massive desmoplastic tissue. Furthermore, objective tumour response does not automatically transcribe into better survival. Therefore, clinical benefit response, a composed parameter consisting of factors like performance status, pain, and body weight was integrated in evaluating tumour response. The aim of this prospective study was to evaluate the usefulness of serial CA 19-9 measurements as a biochemical response marker and an outcome prognostic parameter in patients with advanced pancreatic cancer receiving gemcitabine treatment. A total of 46 consecutive patients (median age 66 years) suffering from histologically proven locally advanced or metastatic adenocarcinoma of the exocrine pancreas were analysed. Gemcitabine was applied for a median of 23 courses (range 6-76). Two patients achieved an objective complete remission, five an objective partial remission (overall response, OR=15.2%), while objective stable disease was documented in 19 and objective progressive disease in 20 patients. Patients with a decrease of >20% of the baseline CA 19-9 level after 8 weeks of chemotherapy had a significantly better median survival than patients with a rise or a decline <20%. The response of CA 19-9 >20% during chemotherapy was the only independent predictor of survival in a multivariate analyses. In contrast, neither objective tumour response nor clinical benefit response showed this level of significance. In conclusion, kinetics of CA19-9 serum concentration serves as an early indicator of response to gemcitabine chemotherapy in advanced pancreatic cancer.
血清糖类抗原19-9(CA 19-9)已被确定为诊断胰腺外分泌癌的一种有用的肿瘤标志物,但其在评估吉西他滨化疗反应方面的价值尚不清楚。由于大量促结缔组织增生性组织,胰腺癌的肿瘤消退很难确定。此外,客观的肿瘤反应并不一定会转化为更好的生存率。因此,临床获益反应,一个由诸如体能状态、疼痛和体重等因素组成的复合参数,被纳入到肿瘤反应评估中。这项前瞻性研究的目的是评估在接受吉西他滨治疗的晚期胰腺癌患者中,连续检测CA 19-9作为生化反应标志物和预后参数的有用性。对46例连续患者(中位年龄66岁)进行了分析,这些患者经组织学证实患有胰腺外分泌腺局部晚期或转移性腺癌。吉西他滨的应用疗程中位数为23个疗程(范围6-76个疗程)。2例患者实现客观完全缓解,5例实现客观部分缓解(总缓解率,OR=15.2%),19例患者记录为客观疾病稳定,20例患者为客观疾病进展。化疗8周后基线CA 19-9水平下降>20%的患者,其总生存期显著长于CA 19-9水平升高或下降<20%的患者。化疗期间CA 19-9下降>20%是多变量分析中唯一的生存独立预测因素。相比之下,客观肿瘤反应和临床获益反应均未显示出这种显著水平。总之,CA19-9血清浓度动力学可作为晚期胰腺癌吉西他滨化疗反应的早期指标。