A Prospective Study of Neoadjuvant Chemotherapy With Gemcitabine/Platinum in Muscle-Invasive or Locally-Advanced Urothelial Carcinoma of Bladder

  • STATUS
    Recruiting
  • End date
    Feb 23, 2022
  • participants needed
    48
  • sponsor
    Samsung Medical Center
Updated on 23 January 2021

Summary

Previously-untreated, high-risk (>T3 and/or N+) muscle-invasive bladder cancer (MIBC) cisplatin 60 mg/m2 on day 1 and gemcitabine 1000 mg/m2 on days 1, 8 and 15. On day 1

Description

Screening numbers are endowed to all patients who sign the informed consent forms. These screening numbers are used as 'Subject Identification Code" along with patient initials. Patients withdrawn from the study retain their screening number. New patients must always be allotted with a new screening number. The study population includes chemotherapy-nave adults with high-risk MIBC. Patients who meet all of the inclusion criteria and none of the exclusion criteria will receive cisplatin 60 mg/m2 on day 1 and gemcitabine 1000 mg/m2 on days 1, 8 and 15. On day 1, adequate hydration and antiemetics are needed. Study chemotherapy will repeat every 4 weeks on an outpatient basis and continued until disease progression, unacceptable toxicity, deterioration of clinical condition, patient refusal, or up to 2 or 3 cycles, depending on the operation schedules.

Patients will be seen every 4 weeks. All study subjects will be also eligible to receive best supportive care (BSC) defined as any standard supportive measures that are not considered a primary treatment of the disease under study, including the use of growth factors (i.e. G-CSF) for myelosuppression, bisphosphonates for management of skeletal metastases, analgesics and transfusion of blood products. BSC will be provided at the discretion of the investigators.

Details
Condition Bladder
Treatment cisplatin, Gemcitabine
Clinical Study IdentifierNCT03061630
SponsorSamsung Medical Center
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Must be aged 20 years or more
Must have histologically or cytologically proven UC of bladder
Must have histological evidence of high-risk muscle-invasive disease (i.e., T2~ T4) or clinically N+ disease. They must be considered to have no other treatment options than radical cystectomy
Must have an ECOG performance status of 0 to 1
Must have a life expectancy of 6 months or more
At least 2 weeks since the last surgical procedures or biopsies prior to enrolment. Subjects must have recovered to <Grade 2 from all acute toxicities or toxicity must be deemed irreversible by the investigator
Adequate marrow function without growth factor support or transfusion dependency
Adequate renal function with serum creatinine 1.5 x ULN or a calculated creatinine clearance 60 mL/min using the Cockcroft-Gault or MDRD formulas
Adequate hepatic function
Must agree to use an adequate method of contraception if the patient is sexually active, during and for 12 weeks after the completion of chemotherapy
Written and voluntary informed consent understood, signed and dated

Exclusion Criteria

Ongoing treatment with an anticancer agent not contemplated in this protocol
Radiologic finding consistent with metastatic disease
Severe medical or phychological illness that preclude participation to study, including any history of clinically relevant coronary artery disease or myocardial infarction within the last 3 years, (NYHA) grade III or greater congestive heart failure, cerebrovascular attack within the prior year, or current serious cardiac arrhythmia requiring medication except atrial fibrillation
Non-tolerable > Grade 2 neuropathy or evidence of unstable neurological symptoms within 4 weeks of Cycle 1 Day 1
Major surgery, other than diagnostic surgery or transurethral resection, within 4 weeks prior to Cycle 1 Day 1, without complete recovery
Double primary cancer of other site(s) or a history of other malignancies, except for cured ones at the discretion of investigator
Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
Subjects who have exhibited allergic reactions to study treatment
Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the Investigator, pose an unacceptable risk to the subject in this study
Subject with legal incapacity or limited legal capacity. Dementia or significantly altered mental status that would limit the understanding or rendering of informed consent and compliance with the requirements of this protocol. Unwillingness or inability to comply with the study protocol for any reason
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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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