Locally Advanced Pancreatic Cancer Treated With ABLAtivE Stereotactic MRI-guided Adaptive Radiation Therapy

Pancreatic Cancer Clinical Trial

— LAP-ABLATE  

Official title:

Locally Advanced Pancreatic Cancer Treated With ABLAtivE Stereotactic MRI-guided Adaptive Radiation Therapy (LAP-ABLATE)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05585554
• Other study ID #: LAP-ABLATE
• Status: Not yet recruiting
• Phase: N/A
• Start date: July 2023
• Est. completion date: December 2028

Study information

• Verified date: October 2022
• Source: Viewray Inc.
• Contact: Hailey Austin
• Phone: 719-924-2494
• Email: haustin[@]viewray.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ablative dose magnetic resonance imaging (MRI) guided hypofractionated radiation therapy delivered using daily adaptive dose planning has shown to improve overall survival, relative to patients receiving lower radiation doses, in patients with locally advanced pancreatic cancer, without increasing the rate of serious gastrointestinal toxicity. The next step is to determine how these results compare to chemotherapy alone.

This is a prospective, randomized controlled trial (2:1) comparing induction chemotherapy followed by ablative Stereotactic MR-guided on-table Adaptive Radiation Therapy (SMART) versus chemotherapy alone in locally advanced pancreatic cancer patients. Overall survival outcomes at 2-years will be evaluated.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 267
• Est. completion date: December 2028
• Est. primary completion date: August 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Locally advanced pancreatic adenocarcinoma or adenosquamous carcinoma as defined by NCCN guidelines.

2. Minimum of 4 months interval from chemotherapy start to administration of the last dose/chemo.

3. Minimum 8 cycles of (m)FOLFIRINOX OR 12 doses of gemcitabine/nab - paclitaxel)

4. No radiographic evidence of local or distant disease progression at any time prior to study enrollment after starting chemotherapy

5. At least 18 years of age

6. ECOG performance status = 1

7. Adequate bone marrow and organ function as defined below:

1. Absolute neutrophil count = 1,000/mcL

2. Platelets = 75,000/mcL

3. Hemoglobin = 8.0 g/dL

4. Total bilirubin = 1.5 x IULN

5. AST(SGOT)/ALT(SGPT) = 3.0 x IULN

8. Women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.

9. Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Exclusion Criteria:

1. CA19-9 > 180 U/mL within 30 days of randomization.

2. Any prior abdominal radiation therapy.

3. History of prior malignancy with the exception of: 1) malignancy treated with curative intent and with no known disease for at least 2 years from treatment to study enrollment, 2) adequately treated carcinoma in situ without evidence of disease (i.e. superficial bladder cancer).

4. Currently receiving any other investigational agents.

5. More than one cytotoxic regimen given for pancreatic cancer.

6. Major abdominal surgery within 4 weeks prior to randomization.

7. Definitive surgery for pancreas cancer completed prior to study enrollment (e.g., Whipple procedure).

8. Subject with planned or scheduled definitive surgery for pancreas at time of study enrollment

9. Grade 3 or greater toxicity during induction chemotherapy that has not resolved to at least grade 2

10. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.

11. Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of study entry.

12. Medical/psychological contraindication to having an MRI scan.

Related Conditions & MeSH terms

• Pancreatic Cancer
• Pancreatic Neoplasms

Intervention

Radiation:
• MRIdian
Stereotactic MRI-guided On-table Adaptive Radiation Therapy delivered on MRIdian linac

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Viewray Inc.

References & Publications (2)

Eaton AA, Karanicolas P, Johnson MChir CD, Bottomley A, Allen PJ, Gonen M. Psychometric Validation of the EORTC QLQ-PAN26 Pancreatic Cancer Module for Assessing Health Related Quality of Life after Pancreatic Resection. JOP. J Pancreas (Online) 2017; 18(1):19-25.

Rudra S, Jiang N, Rosenberg SA, Olsen JR, Roach MC, Wan L, Portelance L, Mellon EA, Bruynzeel A, Lagerwaard F, Bassetti MF, Parikh PJ, Lee PP. Using adaptive magnetic resonance image-guided radiation therapy for treatment of inoperable pancreatic cancer. Cancer Med. 2019 May;8(5):2123-2132. doi: 10.1002/cam4.2100. Epub 2019 Apr 1. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival (OS)	To demonstrate superior 2-year overall survival from date of randomization in ablative MRIdian SMART versus no ablative MRIdian SMART in locally advanced pancreatic cancer patients without disease progression after induction chemotherapy.; A Kaplan-Meier survival curve will be used to report the fraction of subjects living throughout the study	2-years
Secondary	Progression-Free Survival (PFS)	To demonstrate superior progression-free survival at 2 years from date of randomization in ablative MRIdian SMART therapy versus no ablative MRIdian SMART therapy in locally advanced pancreatic cancer patients without disease progression after induction chemotherapy.; A Kaplan-Meier survival curve will be used to report percentage of patients living with pancreatic cancer without disease progression	2-years
Secondary	Local Control (LC)	To compare local control at 2 years from date of randomization in ablative MRIdian SMART therapy versus no ablative MRIdian SMART therapy in locally advanced pancreatic cancer patients without disease progression after induction chemotherapy.; A Kaplan-Meier curve will be used to report percentage of patients with local control of pancreatic cancer	2-years
Secondary	Regional Control (RC)	To compare regional control at 2 years from date of randomization in ablative MRIdian SMART therapy versus no ablative MRIdian SMART therapy in locally advanced pancreatic cancer patients without disease progression after induction chemotherapy.; A Kaplan-Meier curve will be used to report percentage of patients with regional control of pancreatic cancer	2-years
Secondary	Distant Metastasis Free Survival (DMFS)	To compare distant metastasis free survival at 2 years from date of randomization in ablative MRIdian SMART therapy versus no ablative MRIdian SMART therapy locally advanced pancreatic cancer patients without disease progression after induction chemotherapy; A Kaplan-Meier survival curve will be used to report percentage of patients living with pancreatic cancer without distant metastasis	2-years
Secondary	Patient Reported Quality of Life (QoL) using EORTC QLQ-C30 questionnaire	To determine changes in patient-reported quality of life in patients diagnosed with locally advanced pancreatic cancer randomized post-chemotherapy with no disease progression in both study groups.; The EORTC QLQ-C30 Scoring Manual will be followed for scoring.; The QLQ-C30 consists of 28 four-level Likert items (on a scale of 1 - "Not at all" to 4 - "Very much"), and two seven-level Likert items which are scored according to the EORTC scoring guidelines into the 15 domains (Overall health and quality of life on a scale of 1 - "Very Poor" to "7 - Excellent").; High scores in the 28 four-level Likert items indicate worse symptoms and health related QoL.; High scores in the two seven-level Likert items indicate better health and quality of life related QoL.	3-months, 12-months, 24-months
Secondary	Patient Reported Quality of Life (QoL) using EORTC QLQ-PAN26 questionnaire	To determine changes in patient-reported quality of life in patients diagnosed with locally advanced pancreatic cancer randomized post-chemotherapy with no disease progression in both study groups.; The EORTC QLQ-C30 Scoring Manual will be followed for the supplemental QLQ-PAN26 module.; The QLQ-PAN26 consists of 26 four-level Likert items (on a scale of 1 - "Not at all" to 4 - "Very much") which are scored according to draft scoring procedures supplied by EORTC to obtain seven multi-item scale scores consisting of two to four items and nine single-item scores.; Higher scores indicate worse symptoms, function and health related QoL.	3-months, 12-months, 24-months
Secondary	Treatment-related toxicity	To evaluate acute grade 3 or greater treatment-related toxicity (assessed using Common Terminology Criteria for Adverse Events (CTCAE) v5) from randomization in patients diagnosed with locally advanced pancreatic cancer randomized post-chemotherapy with no disease progression in both study groups.	90 days