A phase II study to evaluate the efficacy and safety of Docetaxel-PM in recurrent or metastatic head and neck squamous cell carcinoma

Not Applicable

Completed

• Conditions: Neoplasms

• Registration Number: KCT0003480
• Lead Sponsor: Asan Medical Center

Brief Summary

This trial closed prematurely . A total of 17 patients were enrolled : 16 patients received D PM and 1 4 patients were evaluable for treatment response . The ORR was 6. 3 1 / and disease control rate was 62. 6 % (10/ 16). Median progression free and overall survival times were 2.7 and 5.6months, respectively. Grade 3/4 toxicity were as follows anemia (1 2.5 %), neutropenia 37.5 %), febrile neutropenia(2 5.0 %), arm pain 6. 3 %%), constipation ( 3 %)%), fatigue (1 2.5 %)%), hypercalcemia ( 3 %)%),hypoalbuminemia (6.3%), hypophosphatemia (12.5%), hypokalemia (6.3%), nausea (6.3%) and pneumonia (12.5%). Grade 5 anaphylactic shock, grade 2 infusion related reaction and grade 2 lower extremities edema were observed in 6.3%, 18.8% and 6.3%, respectively.

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-05-31
• Last Update Posted: 23 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

1.Patients who were histologically or cytologically diagnosed as having oral cavity, oropharynx, hypopharynx, or larynx squamous cell carcinoma with recurrent and metastatic evidence and who cannot be treated by salvage surgery or radiotherapy

2.Time of disease progression, regardless of whether that treatment or after platinum-based therapy
?Patients who have disease progression after concurrent chemoradiotherapy of curative purpose
(including induction chemotherapy) including a platinum-based (cisplatin or carboplatin) chemotherapy
? Patients who have disease progression after primary or secondary treatment of palliative purpose including
a platinum-based (cisplatin or carboplatin) chemotherapy

3.Patients who aged 20 years or older and under 79 years old

4.Patients whose Eastern Cooperative Oncology Group (ECOG) performance scores are 0-2

5.Patients who have one measurable lesion at least by RECIST(Response evaluation criteria in solid tumors) criteria 1.1

6.Patients who show adequate function of organ:
?bone marrow: Absolute Neutrophil count (ANC) = 1,500/µL, Platelet count = 100,000/µ, Hb= 9.0 g/dl
(allowed blood transfusion)
?Liver: ? with no evidence of liver metastasis; Total bilirubin = 1.5mg/dl, alkaline phosphatase (ALP),
aspartate transaminase (AST), alanine transaminase (ALT) = 2.0 X upper limit of normal (ULN)
? with liver metastasis; bilirubin = 3.0 X ULN, aspartate transaminase (AST), alanine transaminase (ALT) = 5.0 X ULN
?Kidney: creatinine = 1.5 X ULN

7.Patients who have signed written consent forms prior to participation in the clinical trial

Exclusion Criteria

1. Patients who have Primary tumor of nasopharynx
2. Patients who have received treatment prior regimen of three or more drugs
3. Patients who have Primary malignant tumors of other sites (except if; early cervical cancer,
skin basal cell cancer received appropriate treatment, Malignant tumor without recurrent state treated five years previously)
4. Previous radiotherapy is allowed, patients who should be completed radiotherapy before 4 weeks prior to the
initial administration of the investigational product
5. Patients who have received a major surgery within 4 weeks prior to the initial administration of the investigational product
or patients who does not recover after major surgery
6. Patients who have severe diseases or medical condition as follows
?Congestive heart failure(NYHA class III or IV)
?Unstable angina, cardiac infarction within 6 months
?Second-degree atrioventricular (AV) block or more, clinically cardiac arrhythmia that needs drug therapy
?Uncontrollable Hypertension
?Hepatic cirrhosis (= Child class B)
?Interstitial lung disease
?Mental disorder not to comply with the protocol
?Uncontrolled diabetes
?Uncontrolled ascites or pulmonary edema
?Active infection
7. Pregnant or lactating women
8. Patients considered inappropriate to participating the study by the investigator

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Tumor Response rate

Secondary Outcome Measures

Name	Time	Method
Progression free survival;Disease control rate;Overall survival;Incidence rate of hypersensitivity reaction to Docetaxel-PM;efficacy of Doce-PM