Pilot Study of Chemotherapy for HPV-Associated Oropharyngeal Cancer

Oropharyngeal Squamous Cell Carcinoma Clinical Trial

Official title:

Pilot Study of Induction Chemotherapy Followed by Risk and Response-Stratified Treatment for Locoregional HPV Associated Oropharyngeal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04572100
• Other study ID #: IRB20-0713
• Status: Completed
• Phase: Phase 1
• Start date: October 1, 2020
• Est. completion date: January 9, 2023

Study information

• Verified date: July 2023
• Source: University of Chicago
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Doctors leading this study will give blood tests to head and neck cancer participants during the beginning of chemotherapy treatment (also known as induction therapy) to see if these blood tests can help predict tumor shrinkage after therapy and reduce the amount of additional radiotherapy or chemotherapy treatment the participant may need. This study will also examine ways to reduce overall side effects of treatment using robotic surgery, chemotherapy and radiotherapy, or radiotherapy alone.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: January 9, 2023
• Est. primary completion date: January 9, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects must have clinically confirmed Human papillomavirus(HPV)-positive head and neck squamous cell cancer of the back of the mouth/throat (oropharynx). Confirmed HPV-positive disease of other subsites are uncommon but also eligible.

2. HPV testing must be compliant with the following criteria:

1. P16INK4a immunohistochemistry (p16 IHC) positivity is sufficient to enroll and initiate treatment (p16 IHC interpretation to follow guidelines by Jordan and Lingen et al72).

2. p16 IHC positivity is to be validated using an HPV Polymerase chain reaction (PCR

• a type of DNA copying method).

3. HPV PCR must demonstrate HPV16 or HPV18 subtype

3. Availability of greater than 10 unstained 5 micron slides (to be provided to HTRC at the University of Chicago). Patients who cannot fulfill this requirement will need to undergo a new biopsy prior to enrollment on study.

4. Participants must be at least 18 years old.

5. Participants with American Joint Committee on Cancer (AJCC) (8th edition, 2018) N1 (>=3cm), N2-N3 nodal disease or T3-T4 primary tumor.

6. Measurable disease (either primary site or nodal disease) according to Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 criteria.

7. No previous radiation or chemotherapy for a head and neck cancer.

8. No complete surgical resection for a head and neck cancer within 8 weeks of enrollment (although lymph node biopsy including excision of an individual node with presence of residual nodal disease, or surgical biopsy/excision of the tumor with residual measurable disease is acceptable.) No surgical procedures or biopsies will occur after baseline scans are performed and measurable lesions are identified.

9. Eastern Cooperate Oncology Group performance status 0-1

10. Normal organ function clinically confirmed by medical records.

11. Participants must sign a study-specific informed consent form prior to study entry. Participants should have the ability to understand and the willingness to sign a written informed consent document.

12. Women of childbearing potential must have a negative serum or urine pregnancy test within 24 hours prior to the start of study drug.

13. Women must not be breastfeeding.

14. Women of childbearing potential must agree to follow instructions for method(s) of contraception for the duration of treatment.

15. Men who are sexually active with women of childbearing potential must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug(s).

Exclusion Criteria:

1. Any sign of metastatic disease (M1 disease).

2. Non-HPV16/18 subtype

3. Unidentifiable primary site of cancer.

4. Other medical illnesses that may impair the participant's ability to receive therapy or limit survival. This includes but is not limited to ongoing or active infection, immunodeficiency, symptomatic congestive heart failure, pulmonary dysfunction, cardiomyopathy, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance. Patients with clinically stable and/or chronically managed medical illnesses that are not symptomatic and/or are not expected to impact treatment on protocol are still eligible (conditions to be reviewed by the PI to confirm eligibility)

5. Prior surgical therapy other than incisional/excisional biopsy or organ-sparing procedures such as debulking of airway-compromising tumors. Residual measurable tumor is required for enrollment as discussed above.

6. Patients receiving other investigational agents.

7. Prior systemic anti-cancer treatment within the last 8 weeks.

8. Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer or any tumors that are not likely to influence life expectancy in the subsequent 3 years without active treatment.

9. Has known history of, or any evidence of active, non-infectious pneumonitis.

10. Has a history of HIV.

11. Has known active Hepatitis B or hepatitis C. If eradicated, patient is eligible.

12. Has received a live vaccine within 28 days of planned start of study therapy.

Related Conditions & MeSH terms

• Carcinoma, Squamous Cell
• Oropharyngeal Neoplasms
• Oropharyngeal Squamous Cell Carcinoma
• Squamous Cell Carcinoma of Head and Neck

Intervention

Other:
• Transoral Robotic Surgery (TORS) or Radiotherapy
Participants assigned to this group will receive transoral robotic surgery (TORs) or radiotherapy. Radiotherapy is given once a day for 5 weeks. A percentage of subjects who undergo surgery may need further radiotherapy with or without chemotherapy based on the results of the surgery. TORs is surgery in which a robot with arms is used to remove cancer from hard-to-reach areas of the mouth and throat.
• Chemotherapy and Low-Dose Radiotherapy
Participants assigned to this group will receive 5 weeks of chemotherapy combined with low- dose radiotherapy.
• Chemotherapy and High-Dose Radiotherapy
Participants assigned to this group will receive 7 weeks of chemotherapy combined with high- dose radiotherapy.

Drug:
• Paclitaxel
This drug will be combined with carboplatin during induction therapy for 9 weeks.
• Carboplatin
This drug will be combined with paclitaxel during induction therapy for 9 weeks.

Locations

Country	Name	City	State
United States	University of Chicago Medical Center	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
University of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of collection of serial HPV-DNA blood samples in patients undergoing treatment for Oropharyngeal Squamous Cell Carcinoma	To determine if it is possible (feasibility) to measure HPV-DNA using blood tests among participants undergoing induction chemotherapy followed by a second round of response-based therapy for their HPV-associated cancer. This feasibility will be determined by measuring the proportion of patients who complete chemotherapy treatment and HPV-DNA assessments.	16 weeks
Primary	Relationship Between HPV-DNA Found in Participant's Blood and Participant Response to Chemotherapy	To evaluate the relationship (aka correlation) between the amount of HPV-DNA found in a participant's plasma/blood and the participant's response to induction chemotherapy based on how their tumor responds to treatment.	16 weeks
Secondary	Changes in Blood Containing HPV-DNA During Response-Based Therapy	To evaluate changes in blood containing HPV-DNA during a second round of chemotherapy (known as response-based chemo-radiotherapy) that will be based on how the participant responded to their first/induction phase of chemotherapy treatment. This outcome will be measured by checking quantitative HPV DNA in plasma with each cycle of induction chemotherapy, weekly during radiation treatment, and following completion of radiation at set time points within the study.	16 weeks
Secondary	Side Effects of Cisplatin-Based Chemotherapy Treatment	To evaluate the side effects of weekly cisplatin-based treatment in participants receiving chemotherapy followed by a second round of response-based therapy for their HPV-associated cancer.	16 weeks
Secondary	Tumor Response Among Participants Undergoing Transoral Robotic Surgery	To determine how participant's tumor/cancer responds when they are undergoing Transoral Robotic Surgery (TORS) following induction chemotherapy. TORs is surgery in which a robot with arms is used to remove cancer from hard-to-reach areas of the mouth and throat. Data about how patients' tumors respond in this study will be compared to similar data from a previous study.	20 weeks
Secondary	Time to Disease Recurrence	Length of time participants remain without evidence of disease.	5 years
Secondary	Overall Survival	Length of time until participant death.	5 years
Secondary	Locoregional Control	Number of participants who experience local control of their primary tumors after treatment.	5 years
Secondary	Distant Control	Number of participants who experience control of metastatic disease (distant tumors) after treatment.	5 years