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

Gianni Fornari, Elisa Artusio, Lorenza Mairone, Mario Airoldi, Guido Bongioannini, Enrica Amasio, Claudia Rosmino, Pietro Gabriele

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

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: III, 4.6%; IVA, 63.6%; IVB, 31.8%. Induction carboplatin (AUC = 6) and paclitaxel (200 mg/m2) × 3 cycles (q21 days) were given. Responders received definitive radiotherapy with concurrent carboplatin (35 mg/m2/day from days 1 to 5 in weeks 1, 3, 5 and 7) and paclitaxel (50 mg/m2 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.

Original languageEnglish
Pages (from-to)489-494
Number of pages6
JournalTumori
Volume88
Issue number6
Publication statusPublished - Nov 2002

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Adjuvant Chemoradiotherapy
Carboplatin
Chemoradiotherapy
Paclitaxel
Radiotherapy
Neutropenia
Drug Therapy
Hypopharynx
Mucositis
Oropharynx
Neck Dissection
Alopecia
Larynx
Area Under Curve
Mouth
Weight Loss
Hospitalization
Fever
Carcinoma, squamous cell of head and neck
Survival

Keywords

  • Head and neck carcinoma
  • Paclitaxel
  • Radiotherapy

ASJC Scopus subject areas

  • Cancer Research

Cite this

Fornari, G., Artusio, E., Mairone, L., Airoldi, M., Bongioannini, G., Amasio, E., ... Gabriele, P. (2002). Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma. Tumori, 88(6), 489-494.

Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma. / Fornari, Gianni; Artusio, Elisa; Mairone, Lorenza; Airoldi, Mario; Bongioannini, Guido; Amasio, Enrica; Rosmino, Claudia; Gabriele, Pietro.

In: Tumori, Vol. 88, No. 6, 11.2002, p. 489-494.

Research output: Contribution to journalArticle

Fornari, G, Artusio, E, Mairone, L, Airoldi, M, Bongioannini, G, Amasio, E, Rosmino, C & Gabriele, P 2002, 'Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma', Tumori, vol. 88, no. 6, pp. 489-494.
Fornari G, Artusio E, Mairone L, Airoldi M, Bongioannini G, Amasio E et al. Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma. Tumori. 2002 Nov;88(6):489-494.
Fornari, Gianni ; Artusio, Elisa ; Mairone, Lorenza ; Airoldi, Mario ; Bongioannini, Guido ; Amasio, Enrica ; Rosmino, Claudia ; Gabriele, Pietro. / Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma. In: Tumori. 2002 ; Vol. 88, No. 6. pp. 489-494.
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abstract = "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: III, 4.6{\%}; IVA, 63.6{\%}; IVB, 31.8{\%}. Induction carboplatin (AUC = 6) and paclitaxel (200 mg/m2) × 3 cycles (q21 days) were given. Responders received definitive radiotherapy with concurrent carboplatin (35 mg/m2/day from days 1 to 5 in weeks 1, 3, 5 and 7) and paclitaxel (50 mg/m2 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.",
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T1 - Paclitaxel and carboplatin in neo-adjuvant and concomitant chemoradiotherapy in locally advanced head and neck squamous cell carcinoma

AU - Fornari, Gianni

AU - Artusio, Elisa

AU - Mairone, Lorenza

AU - Airoldi, Mario

AU - Bongioannini, Guido

AU - Amasio, Enrica

AU - Rosmino, Claudia

AU - Gabriele, Pietro

PY - 2002/11

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N2 - 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: III, 4.6%; IVA, 63.6%; IVB, 31.8%. Induction carboplatin (AUC = 6) and paclitaxel (200 mg/m2) × 3 cycles (q21 days) were given. Responders received definitive radiotherapy with concurrent carboplatin (35 mg/m2/day from days 1 to 5 in weeks 1, 3, 5 and 7) and paclitaxel (50 mg/m2 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.

AB - 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: III, 4.6%; IVA, 63.6%; IVB, 31.8%. Induction carboplatin (AUC = 6) and paclitaxel (200 mg/m2) × 3 cycles (q21 days) were given. Responders received definitive radiotherapy with concurrent carboplatin (35 mg/m2/day from days 1 to 5 in weeks 1, 3, 5 and 7) and paclitaxel (50 mg/m2 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.

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