Study Of Nab-Paclitaxel And Gemcitabine With Or Without Tocilizumab In Pancreatic Cancer Patients

Study Overview

Study of Nab-Paclitaxel and Gemcitabine With or Without Tocilizumab in Pancreatic Cancer Patients

This is a multicenter center, 2-arms prospective randomized phase II trial which evaluates whether tocilizumab with gemcitabine/nab-paclitaxel is more effective than gemcitabine/nab-paclitaxel.

The development of new effective treatment strategies remains a major challenge in patients with PC. High levels of IL-6 and presence of a systemic inflammatory response in PC patients have been reported to correlate with worse survival. Preclinical PC models have clearly shown that anti-IL-6-receptor antibody tocilizumab in combination with chemotherapy reduced tumor growth, number of distant metastases and the local recurrence rate. Thus, blockade of IL-6-regulated signaling pathways represents a promising approach in combination with chemotherapy. Elevated C-reactive protein (CRP) alone or in combination with hypoalbuminaemia (Modified Glasgow Prognostic Score - mGPS) are induced by IL-6 and could feasibly represent surrogate markers for IL-6 bioactivity to stratify patients likely to gain benefit through targeting IL-6.

Unresectable Pancreatic Carcinoma

DRUG: Tocilizumab
DRUG: Gemcitabine
DRUG: nab-Paclitaxel

GI1612

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates	Results Reporting Dates	Study Record Updates
First Submitted 2016-05-06	Results First Submitted N/A	Last Update Submitted that met QC Criteria 2023-09-21
First Submitted that Met QC Criteria 2016-05-06	Results First Submitted that Met QC Criteria N/A	Last Update Posted (ACTUAL) 2023-09-22
First Posted (ACTUAL) 2016-05-10	Results First Posted N/A	Last Verified 2023-09

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment

Allocation:
Randomized

Interventional Model:
Parallel

Masking:
None

Arms and Interventions

Participant Group/Arm	Intervention/Treatment
EXPERIMENTAL: Tocilizumab & Gemcitabine and nab-Paclitaxel Tocilizumab: 8 mg/kg given I. V. on day 1 over 60 minutes every 28 day cycle. Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.	DRUG: Tocilizumab Intravenous infusion DRUG: Gemcitabine Intravenous infusion DRUG: nab-Paclitaxel Intravenous infusion,
ACTIVE_COMPARATOR: Gemcitabine and nab-Paclitaxel Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.	DRUG: Tocilizumab Intravenous infusion DRUG: Gemcitabine Intravenous infusion DRUG: nab-Paclitaxel Intravenous infusion,

Participant Group/Arm

Intervention/Treatment

EXPERIMENTAL: Tocilizumab & Gemcitabine and nab-Paclitaxel

Tocilizumab: 8 mg/kg given I. V. on day 1 over 60 minutes every 28 day cycle. Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.

DRUG: Tocilizumab

Intravenous infusion

DRUG: Gemcitabine

Intravenous infusion

DRUG: nab-Paclitaxel

Intravenous infusion,

ACTIVE_COMPARATOR: Gemcitabine and nab-Paclitaxel

Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.

DRUG: Tocilizumab

Intravenous infusion

DRUG: Gemcitabine

Intravenous infusion

DRUG: nab-Paclitaxel

Intravenous infusion,

Primary Outcome Measures	Measure Description	Time Frame
Overall survival at 6 months		Approximately up to 6 months.

Secondary Outcome Measures	Measure Description	Time Frame
Performance status at 3 and 6 months assessed by investigator		Approximately up to 6 months.
Performance status at 3 and 6 months, assessed by patient		Approximately up to 6 months.
Progression free survival (PFS), defined as the time from the date of randomization until the earliest date of disease progression		Randomization to disease progression, or death due to any cause if sooner. Approximately up to 6 months.
Overall survival (OS), defined as the time from the date of randomization until death due to any cause.		Randomization until death due to any cause. Approximately up to 12 months.
Overall response rate (ORR) (ORR = CR + PR), according to RECIST 1.1.RECIST 1.1		Approximately up to 6 months.
Disease control rate (DCR), (DCR = CR + PR + SD), according to RECIST 1.1.		Approximately up to 6 months.
Safety (Data on safety parameters) Safety and tolerability of the treatment regimens assessed by a summary of adverse events and clinical laboratory assessments.		Approximately up to 6 months.
Quality of Life (Quality of Life Questionnaire C30 (QLQ-C30) Version 3.0).		Approximately up to 6 months.

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

Signed informed consent
Histological or cytological pancreatic adenocarcinoma. Malignant unspecified tumor cells in cytological specimen are allowed after investigator assessment, mixed histology including adenosquamous carcinoma is allowed
Male or non-pregnant, non-lactating females who are ≥18 years of age at the time of signing the informed consent form (ICF)
Non-curable unresectable locally advanced or metastatic pancreatic carcinoma.
A modified Glasgow Prognostic Score (mGPS) criteria of 1 or 2 assessed within 14 days of randomization as defined below:
mGPS of 1: CRP > 10 mg/L and albumin ≥ 35 g/L
mGPS of 2: CRP > 10 mg/L and albumin < 35 g/L
No prior antineoplastic chemotherapy or anti-cancer drugs. Patients who have received neoadjuvant or adjuvant chemotherapy and who are diagnosed with loco regional recurrent or metastatic disease are not eligible
ECOG/WHO Performance Status (PS) 0-1
≥ 4 weeks since prior major surgery, ≥ 2 weeks since prior minor surgery and ≥ 1 week since prior radiation therapy
Measurable disease using the RECIST1.1 criteria, defined as lesions that can be measured in at least one dimension and which have not been previously irradiated. Longest diameter ≥ 20 mm with conventional techniques or ≥ 10 mm with spiral CT scan or MRI
Fertile men and women of childbearing potential (defined as a sexually mature woman who (1) has not undergone hysterectomy [the surgical removal of the uterus] or bilateral oophorectomy [the surgical removal of both ovaries] or (2) has not been naturally postmenopausal for at least 24 consecutive months [ie, has had menses at any time during the preceding 24 consecutive months]) must use secure contraception methods as follows: intrauterine device, double-barrier contraception, as a condom and occlusive cap (diaphragm or cervical/vault caps) with a vaginal spermicidal agent (foam/gel/cream/suppository), vasectomized partner who is sterile prior to the female subject's entry and is the sole sexual partner for that female, or complete abstinence from sexual intercourse from before 2 months entering the study until 6 months after end of chemotherapy
Acceptable hematology parameters defined as:
Absolute neutrophil count (ANC) ≥ 1.5 x 10⁹/L
Platelet count ≥ 100 x 10⁹/L
Haemoglobin ≥ 5.6 mmol/L
Acceptable liver function defined as:
Serum bilirubin < 1.5 x upper limit of normal (ULN)
ASAT/ALAT < 2.5 x ULN ( < 5 x ULN with known liver metastasis)
Acceptable renal function with a creatinine clearance ≥ 50 mL/min/ (eg, using the Cockroft-Gault formula)
Subjects must have signed and dated a BIOPAC IRB/IEC approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care

Electrocardiogram (ECG) with significant modifications suggesting a high risk of occurrence of angina pectoris or high risk of arrhythmia.
Other malignancies, except adequately treated basal carcinoma or squamous cell carcinoma of the skin or in-situ cervix carcinoma or incidental prostate cancer (T1a, Gleason score ≤ 6, PSA < 0.5 ng/ml), or any other tumor with a disease free survival of ≥ 5 years.
History of serious or concurrent illness or uncontrolled medical disorder; any medical condition that might be aggravated by chemotherapy treatment or which could not be controlled; including, but not restricted to:
Active infection requiring antibiotics within 2 weeks before the study inclusion
Concurrent congestive heart failure NYHA ( class III - IV )
Unstable angina pectoris, or myocardial infarction within 6 months and/or prior poorly controlled hypertension
Inflammatory bowel disease (colitis, Crohns) or other serious gastrointestinal conditions associated with risk of perforation
Peripheral neuropathy grade ≥ 2 according to CTCAE v 4.0
Concomitant use of immunosuppressive or myelosuppressive medications that would in the opinion of the investigator, increase the risk of serious neutropenic complications.
No known or suspected allergy to the investigational agents or any agents given in association with this trial.
Pregnant or lactating women.
Any psychological, familial, sociological, or geographical condition which does not permit protocol compliance and medical follow-up.
Enrollment in any other clinical protocol or investigational study with an interventional agent or assessments that may interfere with study procedures.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Celgene

Investigators

PRINCIPAL_INVESTIGATOR: Inna Chen, MD, Herlev & Gentofte Hospital

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Chen IM, Johansen JS, Theile S, Silverman LM, Pelz KR, Madsen K, Dajani O, Lim KZM, Lorentzen T, Gaafer O, Koniaris LG, Ferreira AC, Neelon B, Guttridge DC, Ostrowski MC, Zimmers TA, Nielsen D. Randomized Phase II Study of Nab-Paclitaxel and Gemcitabine With or Without Tocilizumab as First-Line Treatment in Advanced Pancreatic Cancer: Survival and Cachexia. J Clin Oncol. 2025 Jun 20;43(18):2107-2118. doi: 10.1200/JCO.23.01965. Epub 2025 May 12.

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