Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma

被引:6
作者
Fornari, G
Artusio, E
Mairone, L
Airoldi, M
Bongioannini, G
Amasio, E
Rosmino, C
Gabriele, P
机构
[1] Osped Evangel Valdese, Div Oncol, I-10125 Turin, Italy
[2] Osped S Giovanni Antica Sede, Div Oncol, Turin, Italy
[3] Osped Mauriziano Umberto 1, ENT Unit, Turin, Italy
[4] IRCC, Turin, Italy
[5] Osped Maria Vittoria, ENT Unit, Turin, Italy
[6] Osped Mauriziano Umberto 1, Radiotherapy Unit, Turin, Italy
来源
TUMORI JOURNAL | 2002年 / 88卷 / 06期
关键词
head and neck carcinoma; paclitaxel; radiotherapy;
D O I
10.1177/030089160208800611
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim and background: To evaluate feasibility of neoadjuvant chemotherapy (NA-CT) followed by CT + radiotherapy (RT) in locally advanced or unresectable head and neck squamous cell carcinoma (HNSCC). Methods: 22 HNSCC patients were enrolled (18 males, 4 females; median age, 59.5 years; median ECOG PS, 1). Sites of disease: oral cavity, 18.2%; oropharynx, 40.9%; hypopharynx, 18.2%; larynx, 4.6%, multiple sites, 18.2%. T (tumor) category: T2, 13.6%; T3, 31.8%; T4, 54.5%. N (nodes) category: NO, 9.1%; N1, 18.1%; N2, 40.9%; N3, 31.8%. Stage: 111, 4.6%; IVA, 63.6%; IVB, 31.8%. Induction carboplatin (AUC = 6) and paclitaxel (200 mg/m(2)) x 3 cycles (q21 days) were given. Responders received definitive radiotherapy with concurrent carboplatin (35 mg/m(2)/day from days 1 to 5 in weeks 1, 3, 5 and 7) and paclitaxel (50 mg/m(2) on days 10, 24 and 38). Patients with node involvement were suggested to undergo postradiotherapy neck dissection. Results: NA-CT 97% of planned chemotherapy cycles were administered. Prevalent toxicity was hematologic: 50% G4 neutropenia and 31.8% G3, one neutropenic fever. All patients had alopecia. Complete responses in T and N were 4 (18.2%) and 3 (15%), respectively. Partial responses were 13 (59%) and 9 (45%). There was 1 progressive disease. CT + RT 79.9% of planned cycles of CT were administered. In 19 patients (86.4%) more than 50% of planned cycles of CT were completed. Median dose of RT was 70.2 Gy on T/N+ and 54 Gy on NO. Limiting toxicity was mucositis in 77.3%, followed by neutropenia (59.1% G3-G4). Median weight loss was 4.9%. 18.2% of patients required hospitalization. Complete responses in T and N were 15 (68.1%) and 8 (40%), respectively. Partial responses were 5 (22.7%) and 7 (35%). Conclusions: The preliminary results of this study are encouraging, despite the toxicity. Adequate follow-up is required to evaluate efficacy in terms of local-regional control and overall survival.
引用
收藏
页码:489 / 494
页数:6
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