Prognostic Role of Circulating Tumor Cells during Induction Chemotherapy Followed by Curative Surgery Combined with Postoperative Radiotherapy in Patients with Locally Advanced Oral and Oropharyngeal Squamous Cell Cancer

被引:56
作者
Inhestern, Johanna [1 ]
Oertel, Katrin [1 ]
Stemmann, Viola [1 ]
Schmalenberg, Harald [2 ]
Dietz, Andreas [3 ]
Rotter, Nicole [4 ]
Veit, Johannes [4 ]
Goerner, Martin [5 ]
Sudhoff, Holger [6 ]
Junghanss, Christian [7 ]
Wittekindt, Claus [8 ]
Pachmann, Katharina [9 ]
Guntinas-Lichius, Orlando [1 ]
机构
[1] Jena Univ Hosp, Dept Otorhinolaryngol, Jena, Germany
[2] Jena Univ Hosp, Univ Tumor Ctr, Jena, Germany
[3] Univ Med Ctr Leipzig, Dept ENT Surg, Leipzig, Germany
[4] Univ Ulm, Med Ctr, Dept Otorhinolaryngol Head & Neck Surg, D-89069 Ulm, Germany
[5] Acad Teaching Hosp Bielefeld, Dept Hematol & Oncol, Bielefeld, Germany
[6] Acad Teaching Hosp Bielefeld, Dept Otorhinolaryngol Head & Neck Surg, Bielefeld, Germany
[7] Univ Rostock, Dept Hematol Oncol & Palliat Med, Div Med, D-18055 Rostock, Germany
[8] Univ Hosp Giessen & Marburg, Dept Otorhinolaryngol Head & Neck Surg, Giessen, Germany
[9] Jena Univ Hosp, Div Hematol & Internal Oncol, Clin Internal Med 2, Jena, Germany
来源
PLOS ONE | 2015年 / 10卷 / 07期
关键词
ADVANCED HEAD; NECK-CANCER; BONE-MARROW; PHASE-III; CARCINOMA; FLUOROURACIL; CISPLATIN; PROGRESSION; SURVIVAL; BLOOD;
D O I
10.1371/journal.pone.0132901
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The prognostic role of circulating tumor cells (CTCs) after induction chemotherapy using docetaxel, cisplatin and fluorouracil (TPF) prior to surgery and adjuvant (chemo) radiation in locally advanced oral squamous cell cancer (OSCC) was evaluated. Methods In this prospective study, peripheral blood samples from 40 patients of the phase II study TISOC-1 (NCT01108042) with OSCC before, during, and after treatment were taken. CTCs were quantified using laser scanning cytometry of anti-epithelial cell adhesion molecule-stained epithelial cells. Their detection was correlated with clinical risk factors, recurrencefree (RFS) and overall survival (OS). Results Before starting the treatment CTCs were detected in 32 of 40 patients (80%). The median number at baseline was 3295 CTCs/ml. The median maximal number of CTCs during treatment was 5005 CTCs/ml. There was a significant increase of CTCs before postoperative radiotherapy compared to baseline before 1st cycle of IC (p = 0.011), 2nd cycle of IC (p = 0.001), 3rd cycle of IC (p = 0.004), and before surgery (p = 0.002), but not compared to end of therapy (p = 0.118). CTCs at baseline >median was also associated to risk of recurrence (p = 0.014). Maximal CTCs during therapy >median was more frequently observed in tumors of the oral cavity (p=0.022) and related to higher risk of death during follow-up (p = 0.028). Patients with CTCs at baseline >median value had significant lower RFS than patients with CTCs at baseline <median value (p = 0.025). Patients with maximal CTCs values >median during the complete course of therapy had a significantly lower OS than patients with values <median (p = 0.049). Finally, the multivariate analysis revealed that OS was significantly lower in patients with maximal CTCs during treatment higher than the median value (HR=6.151; CI: 1.244-30.420). Conclusions Baseline CTCs and maximal CTCs during therapy both seem to be good prognostic markers for OSCC when treated by TPF induction chemotherapy, surgery, and postoperative (chemo)radiation.
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