Concomitant chemoradiotherapy versus induction docetaxel, cisplatin and 5 fluorouracil (TPF) followed by concomitant chemoradiotherapy in locally advanced head and neck cancer: a phase II randomized study

被引:137
作者
Paccagnella, A. [1 ]
Ghi, M. G. [1 ]
Loreggian, L. [2 ]
Buffoli, A. [3 ]
Koussis, H. [4 ]
Mione, C. A. [5 ]
Bonetti, A. [6 ]
Campostrini, F. [7 ]
Gardani, G. [8 ]
Ardizzoia, A. [9 ]
Dondi, D. [10 ]
Guaraldi, M. [11 ]
Cavallo, R. [12 ]
Tomio, L. [13 ]
Gava, A. [14 ]
机构
[1] Osped Angelo, Dept Med Oncol, I-30100 Venice, Italy
[2] Ist Ric & Cura Carattere Sci, Ist Oncol Veneto, Dept Radiotherapy, Padua, Italy
[3] Azienda Osped Univ, Dept Radiotherapy, Udine, Italy
[4] IRCCS, Ist Oncol Veneto, Dept Med Oncol, Padua, Italy
[5] Osped SS Giovanni e Paolo, Dept Radiotherapy, Venice, Italy
[6] Osped Mater Salutis, Dept Med Oncol, Legnago, Italy
[7] Osped Mater Salutis, Dept Radiotherapy, Legnago, Italy
[8] S Gerardo Hosp, Dept Radiotherapy, Monza, Italy
[9] S Gerardo Hosp, Dept Med Oncol, Monza, Italy
[10] Sanofi Aventis, Milan, Italy
[11] St Orsola Marcello Malpighi Hosp, Dept Med Oncol, Bologna, Italy
[12] P Cosma Hosp, Dept Med Oncol, Padua, Italy
[13] Santa Chiara Hosp, Dept Radiotherapy, Trento, Italy
[14] Osped Ca Foncello, Dept Radiotherapy, Treviso, Italy
关键词
concomitant chemoradiotherapy; head and neck cancer; induction chemotherapy; NEOADJUVANT CHEMOTHERAPY; FLUOROURACIL; TRIAL; PRESERVATION; METAANALYSES;
D O I
10.1093/annonc/mdp573
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients and methods: Patients with stage III-IVM0 SCCHN, Eastern Cooperative Oncology Group performance status of zero to one, were randomly assigned to receive CT/RT alone (arm A: two cycles of cisplatin 20 mg/m(2), days1-4, plus 5-fluorouracil 800 mg/m(2)/day 96 h continuous infusion, during weeks 1 and 6 of radiotherapy) or three cycles of TPF (arm B: docetaxel 75 mg/m(2) and cisplatin 80 mg/m(2), day 1, and 5-fluorouracil 800 mg/m(2)/day 96 h continuous infusion, every 3 weeks) followed by the same CT/RT. The primary end point was the rate of radiologic complete response (CR) at 6-8 weeks after the end of CT/RT. Results: A total of 101 patients were randomly allocated to the study (51 arm A; 50 arm B). CR rates were 21.2% (arm A) versus 50% (arm B). Median progression-free survival and overall survival were, respectively, 19.7 and 33.3 months (arm A) and 30.4 and 39.6 months (arm B). Hematologic and non-hematologic toxic effects during CT/RT were similar in the two arms. Conclusion: Induction TPF followed by CT/RT was associated with higher radiologic CR in patients with locally advanced SCCHN with no negative impact on CT/RT feasibility.
引用
收藏
页码:1515 / 1522
页数:8
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