Triplet induction chemotherapy followed by less invasive surgery without reconstruction for human papillomavirus-associated oropharyngeal cancers: Why is it successful or unsuccessful?

Free-flap reconstruction HPV Induction chemotherapy Less invasive surgery Oropharyngeal cancer Pathological complete response

Journal

International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 20 12 2020
accepted: 23 02 2021
pubmed: 9 3 2021
medline: 9 3 2021
entrez: 8 3 2021
Statut: ppublish

Résumé

De-escalating treatments have been focused on for HPV-associated oropharyngeal squamous cell carcinoma (OPSCC). We assessed the efficacy of a triplet induction chemotherapy (ICT) followed by surgery with or without neck dissection (ND) for locally advanced OPSCC, aiming at less invasive surgery without free-flap reconstruction and avoiding postoperative irradiation. This was a retrospective study of 41 patients with advanced resectable HPV-positive OPSCC who underwent ICT followed by surgery of primary resection with or without ND. Patients underwent triplet ICT, including docetaxel, cisplatin, and 5-fluorouracil, or carboplatin, paclitaxel, and cetuximab. Twenty-nine patients had tonsillar cancer, 15 patients were current smokers, and 18 and 12 patients had T2N1M0 and T1N1M0 status (UICC 8th), respectively. After ICT, a surgical procedure without free-flap reconstruction and tracheostomy was possible in 90.2%. Pathological complete response at both the primary site and lymph nodes was achieved in 73.2%. Of the patients who underwent surgery, no adjuvant radiotherapy was required in 85.0%. Two patients (4.9%) experienced recurrence at regional lymph nodes, but were cured by salvage ND followed by adjuvant radiotherapy. Upfront ICT using highly responsive triplet chemotherapeutic regimens may enable us to perform less invasive surgery without free-flap reconstruction and to avoid postoperative irradiation to the locoregional field through excellent postoperative pathological features.

Sections du résumé

BACKGROUND BACKGROUND
De-escalating treatments have been focused on for HPV-associated oropharyngeal squamous cell carcinoma (OPSCC). We assessed the efficacy of a triplet induction chemotherapy (ICT) followed by surgery with or without neck dissection (ND) for locally advanced OPSCC, aiming at less invasive surgery without free-flap reconstruction and avoiding postoperative irradiation.
METHODS METHODS
This was a retrospective study of 41 patients with advanced resectable HPV-positive OPSCC who underwent ICT followed by surgery of primary resection with or without ND. Patients underwent triplet ICT, including docetaxel, cisplatin, and 5-fluorouracil, or carboplatin, paclitaxel, and cetuximab.
RESULTS RESULTS
Twenty-nine patients had tonsillar cancer, 15 patients were current smokers, and 18 and 12 patients had T2N1M0 and T1N1M0 status (UICC 8th), respectively. After ICT, a surgical procedure without free-flap reconstruction and tracheostomy was possible in 90.2%. Pathological complete response at both the primary site and lymph nodes was achieved in 73.2%. Of the patients who underwent surgery, no adjuvant radiotherapy was required in 85.0%. Two patients (4.9%) experienced recurrence at regional lymph nodes, but were cured by salvage ND followed by adjuvant radiotherapy.
CONCLUSIONS CONCLUSIONS
Upfront ICT using highly responsive triplet chemotherapeutic regimens may enable us to perform less invasive surgery without free-flap reconstruction and to avoid postoperative irradiation to the locoregional field through excellent postoperative pathological features.

Identifiants

pubmed: 33683512
doi: 10.1007/s10147-021-01894-z
pii: 10.1007/s10147-021-01894-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1039-1048

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Auteurs

Tomoya Yokota (T)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8777, Japan. t.yokota@scchr.jp.

Tetsuro Onitsuka (T)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Satoshi Hamauchi (S)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8777, Japan.

Hiromichi Shirasu (H)

Division of Medical Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Yusuke Onozawa (Y)

Division of Medical Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Yoshiyuki Iida (Y)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Tomoyuki Kamijo (T)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Takashi Mukaigawa (T)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Shinichi Okada (S)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Yuki Irifune (Y)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Kotaro Ishida (K)

Division of Head and Neck Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Hirofumi Ogawa (H)

Division of Radiation Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Tsuyoshi Onoe (T)

Division of Radiation Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Classifications MeSH