A Study of Toripalimab as Consolidation Therapy After Postoperative Chemoradiotherapy in HNSCC

  • STATUS
    Recruiting
  • End date
    May 1, 2027
  • participants needed
    41
  • sponsor
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Updated on 15 October 2021

Summary

This study is a phase II, open label, single-arm and exploratory clinical trial. The purpose of this study is to observe the efficacy and safety of consolidation immunotherapy with Toripalimab following postoperative radiotherapy or chemoradiotherapy for patients with locally advanced head and neck squamous cell carcinomas (HNSCC).

Details
Condition Head and Neck Squamous Cell Carcinomas
Treatment Consolidation Toripalimab
Clinical Study IdentifierNCT04992559
SponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Last Modified on15 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Postoperative with adverse prognostic factors in patients with locally advanced head and neck squamous cell carcinoma
Have received postoperative adjuvant radiotherapy (chemo) therapy, and the end of the treatment is not more than 2 months
Greater than or equal to 18 and less than 70 years of age at time of study entry
ECOG performance status of 0 or 1
Measurable disease as per RECIST 1.1
Screening labs must meet the following criteria and must be obtained within 14 days prior to registration
Adequate hepatic and renal function as demonstrated by
Serum creatinine < 1.5 X ULN or CrCl > 40mL/min (if using the Cockcroft-Gault formula below)
Males: Creatinine CL (mL/min) = (Weight (kg) x (140 - Age))/(72 x serum creatinine (mg/dL)
Females: Creatinine CL (mL/min) = (Weight (kg) x (140 - Age))/(72 x serum creatinine (mg/dL))x 0.85 2. AST/ALT 3 x ULN 3. Total Bilirubin 1.5 x ULN (except subjects with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL) 2. Adequate bone marrow function as demonstrated by
Absolute Neutrophil Count >1,500/L
Platelets > 100 X 103/L
Hemoglobin > 9.0 g/dL
Women of reproductive potential should have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]) within 7 days of study enrollment
Women of reproductive potential must use highly effective contraception methods to avoid pregnancy for 3 months after the last dose of study drugs; "women of reproductive potential" is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy or bilateral oophorectomy) or who is not postmenopausal; menopause is defined clinically as 12 months of amenorrhea in a woman over 45 in the absence of other biological or physiological causes; in addition, women under the age of 55 must have a documented serum follicle stimulating hormone (FSH) level less than 40 mIU/mL
Men of reproductive potential who are sexually active with women of reproductive potential must use any contraceptive method with a failure rate of less than 1% per year; men who are receiving the study medications will be instructed to adhere to contraception for 3 months after the last dose of study drugs; men who are azoospermic do not require contraception
Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable)
Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up

Exclusion Criteria

Is currently participating in or has participated in a study of an investigational agent within 4 weeks of the first dose of treatment or has not recovered (i.e., Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier
Has had another known invasive malignancy within the previous 5 years With the exception of basal cell carcinoma of the skin, carcinoma in situ of the cervix, and papillary carcinoma of the thyroid, which has been cured
If subject received major surgery for any other reason, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy
Active, known or suspected autoimmune disease
Has evidence of interstitial lung disease or active, non-infectious pneumonitis
Has an active infection requiring systemic therapy
Has received prior therapy with an anti-PD-1 antibody
A history of allergic reaction attributed to compounds of similar chemical or biologic composition to the treatment or other agents used in the study
Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 23 weeks after the last dose of trial treatment
Has a known history of Human Immunodeficiency Virus (HIV) infection (HIV 1/2 antibodies)
Has known active Hepatitis B or C
Known history of active TB ( bacillus tuberculosis )
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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