Overview

Nab-paclitaxel and Gemcitabine, in Elderly Patients Untreated Metastatic Pancreatic Adenocarcinoma

Status:
Completed
Trial end date:
2019-03-01
Target enrollment:
0
Participant gender:
All
Summary
Cancer incidence is increasing with age and the likelihood of elderly suffering from cancer is 1:3. Although many clinical trials include elderly patients, no results for this subgroup of patients are available. Since there is no specific recommendations for treatment of elderly patients with pancreatic cancer, treatment with gemcitabine alone is the treatment of choice for these patients. Single-agent gemcitabine is the current standard of care, but the addition of cytotoxic and targeted agents to gemcitabine has almost invariably provided no significant survival improvement. Results obtained recently in the MPACT phase III clinical trial in patients with pancreatic cancer treated with nab-paclitaxel combined with gemcitabine have shown improvement in overall survival, but due to in this clinical trial was included patients between 27 and 88 years, it is considered necessary to conduct a specific study for patients over 70 years. The aim of this study is to investigate whether the clinical benefit of nab-paclitaxel associated with gemcitabine can be extended to elderly patients with pancreatic cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Asociación de Oncología Médica del Hospital de Cruces
Collaborators:
Apices Soluciones S.L.
Celgene
Treatments:
Albumin-Bound Paclitaxel
Gemcitabine
Paclitaxel
Criteria
Inclusion Criteria:

- Histologically or cytologically-confirmed pancreatic adenocarcinoma

- Stage IV disease (metastatic only)

- No prior systemic therapy for their diagnosis (except in adjuvant setting > six months
previously)

- ECOG performance status of 0-1

- Age >=70 years.

- Evidence of either or both of the following:

- RECIST-defined measurable disease (lesions that can be accurately measured in at
least one dimension with the longest diameter >= 20mm using conventional
techniques or >= 10 mm with spiral CT scan)

- An elevated serum CA19-9 at baseline ( >= 2X ULN)

- Female patients must be either surgically sterile or postmenopausal.

- Male patients must be surgically sterile or must agree to use a condom during sex with
women who may become pregnant while receiving the study drug and for 6 months after
receiving the last dose.

- Adequate bone marrow function:

- ANC >= 1500/uL

- platelet count >= 100,000/uL

- hemoglobin >= 9.0 g/dL

- Adequate hepatic function:

- Total bilirubin <= 1.5 X ULN

- AST (SGOT) <= 2.5 X ULN

- ALT (SGPT) <= 2.5 X ULN

- Adequate renal function as determined by either:

- Serum creatinine <= 1.5 X ULN

- Calculated or measured creatinine clearance >= 40 mL/min (for calculated
creatinine clearance, Cockroft-Gault equation will be used).

- Ability to understand the nature of this study protocol and give written informed
consent

- Willingness and ability to comply with scheduled visits, treatment plans, laboratory
tests, and other study procedures.

Exclusion Criteria:

- Any prior systemic or investigational therapy for metastatic pancreatic cancer.

- Inability to comply with study and/or follow-up procedures.

- History of other disease, metabolic dysfunction, physical examination finding, or
clinical laboratory finding giving reasonable suspicion of a disease or condition
that, in the opinion of the investigator, renders the subject at high risk from
treatment complications or might affect the interpretation of the results of the
study.

- Presence of central nervous system or brain metastases.

- Life expectancy < 12 weeks.

- Pregnancy (positive pregnancy test) or lactation.

- Prior malignancy except for adequately treated basal cell skin cancer, in situ
cervical cancer, adequately treated Stage I or II cancer from which the patient is
currently in complete remission, or any other form of cancer from which the patient
has been disease-free for 5 years.

- Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic
coronary artery disease and cardiac arrhythmias not well controlled with medication)
or myocardial infarction within the last 12 months.

- Lack of physical integrity of the upper gastrointestinal tract or malabsorption
syndrome.

- Known, existing uncontrolled coagulopathy.

- Pre-existing sensory neuropathy > grade 1.

- Major surgery within 4 weeks of the start of study treatment, without complete
recovery.

- Concurrent/pre-existing use of anticoagulant treatment.