Induction Chemotherapy Followed by Surgery for Locally Advanced Head and Neck Cancer

The current standard of care for advanced (stage III and IV) oropharyngeal squamous cell
carcinoma are concomitant chemoradiation, or surgery followed by adjuvant radiation therapy
with or without concomitant chemotherapy. These approaches have persistent and significant
lifelong side effects and sequella related to treatment, and in particular radiotherapy. The
side effects of radiotherapy (augmented with concomitant chemotherapy) include soft tissue
fibrosis, loss of salivary function, dry mouth, life long disturbed taste function, poor
dental health with rapidly decaying teeth, dysfunction of swallowing, significant loss of the
mobility of the base of tongue and pharyngeal constrictors, loss of laryngeal elevation,
esophageal stricture, and at times severe side effects such as soft tissue necrosis or
osteoradionecrosis of the mandible. About 10% of the patients undergoing chemoradiation for
oropharyngeal cancer develop long term swallowing dysfunction with feeding tube dependency.
As a result , patient's quality of life (QOL) is adversely affected. Improvements in the side
effect profile of treatment, the functional outcome, and the QOL remain very important areas
of advancement in treating this patient population. Improvements in functional outcome need
to be achieved while maintaining or improving the oncologic outcome and cure rates for
cancer, compared to the standard of care.

Use of new Taxane based chemotherapy along with Platinum drugs (Cisplatin and Carboplatin) in
high dose neoadjuvant setting, coupled with novel minimally invasive Transoral Laser
Microsurgery (TLM) and Transoral Robotic Assisted Surgery (TORS), allows potential for
improved oncologic outcome as well as avoidance of long term sequalla of high dose radiation
therapy to head and neck. These transoral surgical approaches (TLM and TORS) provide improved
functional outcome compared with traditional open composite resections and complex
reconstructive algorithms for oropharynx. TLM and TORS are currently in clinical use for
early (stage T1 and T2 with N0 or N+ve) oropharyngeal cancer.

An area not adequately or at all investigated in treating moderately advanced oropharyngeal
cancer is combining neoadjuvant high dose chemo-induction followed by minimally invasive
transoral surgery (TLM and TORS) and neck dissection as the definitive treatment.

This approach has the potential for far improved functional outcome by avoiding short and
more importantly long term and permanent sequella of radiation therapy in oropharyngeal
cancer treatment. This approach is a new paradigm in treatment of oropharyngeal cancer, and
can significantly improve the functional outcome of cancer treatment.

Inclusion Criteria:

- Biopsy proven squamous cell carcinoma of the oropharynx (tonsil, base of tongue,
vallecula, soft palate) and supraglottis.

- Stages III (T1N1, T2N1, T3N0, T3N1) and stage IVA (T1N2, T2N2, T3N2, very select
earlyT4) disease not previously treated with any method (Surgery, Radiation or
Chemotherapy)

- No evidence of distant metastatic disease

- Fit for surgery and primary tumor assessed surgically resectable (by surgical PI) via
transoral approach

- Age > 18 years

- Karnofsky performance status > 60%, or ECOG < 2

- ANC > 2,000, platelets > 100,000 and calculated creatinine clearance >50 cc/min

- Signed study specific consent form

- Protocol begins within 4 weeks of biopsy and within 3 weeks of the latest medical
imaging.

- No other malignancies except cutaneous basal or squamous cell cancer within the
last 5 years

- Patients must have measurable disease based on RECIST.

- Men and women of child bearing potential must agree to use effective contraception
while on the study, and women must have a negative pregnancy test, and not be
lactating.

Exclusion Criteria:

- Patients with advanced T4 cancer judged unresectable by transoral approach by surgical
PI.

- Patients with N3 disease (Stage IVB).

- Patients with distant metastatic disease (Stage IVC).

- Patients with radiologically positive neck nodes with radiological evidence of
extracapsular nodal tumor invasion.

- Patients having anatomy not allowing transoral access and exposure for surgery(Judged
by the surgical PI at the time of biopsy under general anesthesia)

- Patients with prior head and neck cancer at any time (other than basal or squamous
cell cancer of the skin)

- Coexistent second malignancy or history within 5 years of prior malignancy (other than
basal or squamous cell cancer of the skin or curatively treated Stage I carcinoma of
the cervix) renders the patient ineligible.

- Patients with peripheral neuropathy >/= grade 1 will not be eligible for the study.

- Patients who have had prior Taxanes or Cisplatin

- Patients with concurrent infection are not eligible. All patients must be afebrile for
at least 3 days prior to start of therapy unless fever is due to tumor.

- Patients with coexisting medical illness of a severity that might interfere with
treatment or follow-up, or who do not have the ability to give informed consent.

- Patients who have received prior radiation therapy, surgery and chemotherapy for the
tumor being treated.

- Patients must not be receiving any other investigational agent while on the study.