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Study: Results from the POLO trial: Olaparib may delay cancer progression in metastatic pancreatic cancer patients with BRCA mutations.

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Contents

At a glance Questions for your doctor
Findings     In-depth                 
Clinical trials Limitations
Guidelines Resources


STUDY AT A GLANCE

This study is about:

whether prolongs disease-free survival for patients with pancreatic cancer who have mutations

Why is this study important?

People with pancreatic cancer have poor survival rates and do not respond well to current treatments. is a type of drug known as a PARP inhibitors that has received approval to treat advanced breast and ovarian cancers in people with mutations. This clinical trial looked at whether the olaparib can improve outcomes for men and women with pancreatic cancer after platinum-based chemotherapy.

Study findings: 

  • Participants taking had progression-free survival that was twice as long as those on (7.4 months among the group and 3.8 months among the group).
     
  • At the trial’s interim evaluation point, there was no difference in the overall survival among the and groups.
     
  • Cancer decreased in size during the trial in the 23% of the group participants and 12% of the group participants.
     
  • Two patients from the group had a complete response at the time of publication.
     
  • There was no difference in health-related quality of life between participants taking and those taking .
     
  • Toxic side effects were more common among participants taking (40%) than among those taking (23%).

What does this mean for me?

If you or a relative have pancreatic cancer, you may want to consider testing, because testing positive for a mutation may change treatment options. 

Note: This information has been updated. On December 27, 2019 the approved the olaparib (Lynparza) as a for patients with pancreatic cancer and a known or suspected mutation whose disease has not progressed after completing chemotherapy.

Posted 7/3/19

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References

Goaln T, Hammel P, Reni M, et al. “Maintenance for BRCA-Mutated Pancreatic Cancer.New England Journal of Medicine. June 2, 2019. DOI: 10.1056/NEJMoa1903387

Commentary: https://www.practiceupdate.com/c/d408f655-53bf-4f04-abdb-1bc79b5edb25?elsca1=soc_share-this-email&elsca2=social&elsca3=email

Pihlak R, Valle JW, McNamara MG. " mutations in pancreatic cancer and potential new therapeutic options." Oncotarget. 2017 Sep 22; 8(42): 73240–73257.
 

Disclosure

FORCE receives funding from industry sponsors, including companies that manufacture cancer drugs, tests and devices. All XRAYS articles are written independently of any sponsor and are reviewed by members of our Scientific Advisory Board prior to publication to assure scientific integrity.

This article is relevant for:

People diagnosed with pancreatic cancer who have a BRCA mutation

This article is also relevant for:

people with metastatic or advanced cancer

people with a genetic mutation linked to cancer risk

people with pancreatic cancer

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IN-DEPTH REVIEW OF RESEARCH

Study background:

Pancreatic cancer has already metastasized in over half of people who are diagnosed . pancreatic cancer does not respond well to current standard of care treatment, which is surgery followed by radiation or chemotherapy, often modified with FOLFIRINOX (leucovorin/5-FU/irinotecan/oxaliplatin). On average, standard chemotherapy care produces progression-free survival of 6 months. About 9% of patients survive 5 years after initial diagnosis. Given the poor response of pancreatic cancer, researchers have been exploring treatments that can improve outcomes.

In people with mutation who have breast or ovarian cancer, PARP inhibitors, in particular (also called Lynparza), can be an effective and maintenance treatments that prolong progression-free survival. The POLO trial (Pancreas Cancer Ongoing) was designed to test whether is useful in treating pancreatic cancer after platinum-based chemotherapy. Between 5 and 10% of patients with pancreatic cancer have an inherited gene mutation.

Researchers of this study wanted to know:

Whether as a maintenance treatment after platinum-based chemotherapy improved progression-free survival of pancreatic cancer patients who had an inherited mutation.

Populations looked at in this study:

Patients were eligible for this clinical trial if they had an inherited or mutation and had confirmed pancreatic cancer that did not progress during their initial platinum-based chemotherapy.

This study involved 3,315 confirmed pancreatic cancer patients from 119 medical sites in 12 countries who were screened for mutations.

Of the 3,315 patients, 247 (7.5%) had an inherited mutation. Patients whose disease progressed while on chemotherapy during the evaluation process were ineligible for the clinical trial.

About two-thirds of the 154 eligible male and female participants had a mutation in and one-third had a mutation in . Average age was 57 years.

Participants were randomly assigned to receive (90 of 92) or (61 of 62). One participant assigned to and one assigned to did not meet eligibility at the start of the trial (due to disease progression), and one assigned to withdrew prior to the start of the trial.

Study design:

This clinical trial was a , double-blind, phase 3 trial.

Participants were randomly assigned to take either or placebo; they were unaware during the trial which they received.

Participants receiving took 300 mg tablets twice a day. Those receiving had look-alike tablets but without . Treatment with both pills continued until the participant's cancer progressed, they had unacceptable toxic side effects or the participant died.

The primary end point of this trial was progression-free survival. Participants were evaluated for disease progression by or CT imaging every 8 weeks for 40 weeks and then every 12 weeks until disease progression was observed. The imaging data was evaluated by an independent reviewer who did not know whether participants were receiving or .

Secondary end points included health-related quality of life, overall survival and objective response rate. Participants filled out a questionnaire every 4 weeks to evaluate health-related quality of life.

This clinical trial was funded by AstraZeneca, a division of Merck, and others and run under oversight as POLO ClinicalTrials.gov (NCT02184195). 

Study findings:

The main finding of this clinical trial was that participants taking experienced prolonged progression-free survival that was twice as long as those on .

  • Participants taking had 7.4 months on average before disease progression occurred.
     
  • Participants taking had 3.8 months on average before disease progression occurred.

The data on overall survival was not fully complete at the time of this publication (46% of patients had died).

  • At this interim evaluation point, there was no difference in the overall survival among the and groups (18.9 months survival with and 18.1 months survival with ).

The objective response rate (ORR)—whether the cancer decreased in size during the trial was evaluated by blinded, independent reviewers.

  • 18 of 78 patients (23%) in the group had decreased tumor size.
  • 6 of 52 patients in the group (12%) had decreased tumor size.
     
  • Two patients from the group had a complete response. No cancer was observable in these two patients at the time of publication.

Quality of life evaluations were similar in both groups:

  • There was no difference in health-related quality of life between participants taking and those taking .

Adverse events including toxic side effects were more common among participants taking than among those taking placebo:

  •  40% of participants taking had severe adverse events.
  • 23% of participants taking had severe adverse events.

Limitations:

This trial had several limitations.

Participants did not include anyone who had cancer that grew during their first platinum-based chemotherapy treatment or anyone who had extended chemotherapy. For this reason, the patients in this trial may not completely represent all of those that would be treated with this drug.

Participants were screened for mutations. Other mutations that may affect pancreatic cancer were not evaluated to determine whether might be useful as a treatment.

Initial results showed that overall survival was not improved among those taking compared to those taking . Patients in the group who had cancer that grew during the trial sometimes took other drugs. Changes in which therapy some participants received may affect their survival: 9 patients who were in the group (15%) took a after disease progression during the trial.

Conclusions:

This clinical trial shows that may improve progression-free survival for patients with pancreatic cancer that had not progressed on platinum-based chemotherapy.

Share your thoughts on this XRAYS article by taking our brief survey.

Posted 7/3/19

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Expert Guidelines
Expert Guidelines

National Comprehensive Cancer Network (NCCN) guidelines recommend the following for people diagnosed with pancreatic cancer:

  • Receive treatment from a team of healthcare professionals that includes a variety of experts in cancer care, genetics, mental health, nutrition and management of side effects. These experts are more likely to be found at large cancer centers that have extensive experience treating pancreatic cancer.
  • Make sure you have had the following tests:
    • Genetic testing for an . Genetic test results may help you and your doctor decide on the best treatment. Genetic test results may also help your relatives understand their risk for cancer. 
    • Imaging tests to learn the of your cancer.  is needed to plan and monitor your treatment. These tests determine whether the tumor can be removed with surgery (it is resectable), if the cancer has spread to nearby organs or (it is locally advanced) or has spread to other parts of the body (it has metastasized).
    • Tumor testing for people with locally advanced or pancreatic cancer can also be used to make treatment decisions and/or determine if you are eligible for clinical trials. 
  • Keep a copy of all test results (online patient portals are a great way to access test results). This will come in handy during a second opinion, if necessary. 
  • Discuss with your healthcare team whether chemotherapy is recommended before and/or after your surgery.

Updated: 11/13/2023

Questions To Ask Your Doctor
Questions To Ask Your Doctor

  • How do I get genetic testing for a mutations?
  • Does carrying a mutation in or another gene change your treatment recommendations for me?
  • Should I have testing?
  • Which treatment is the best for me?
  • Will my insurance pay for Lynparza to treat my pancreatic cancer?
  • Is there a clinical trial that I can join?

Open Clinical Trials
Open Clinical Trials

The following treatment studies are enrolling people diagnosed with pancreatic cancer.

The following vaccine studies are enrolling people with pancreatic cancer.

  • NCT05111353: Neoantigen Vaccines in Pancreatic Cancer in the Window Prior to Surgery. This study looks at the safety of an neoantigen vaccines for pancreatic cancer patients following chemotherapy. Participants receive either the vaccine following by chemotherapy and surgery or the vaccine after  chemotherapy and before surgery.

Other clinical trials for people with pancreatic cancer can be found here.

Updated: 08/15/2023

Open Clinical Trials
Open Clinical Trials

The following studies look at treatment for people with advanced

 

Updated: 02/01/2024

Peer Support
Peer Support

The following organizations offer peer support services for people with or at high risk for pancreatic cancer:

Updated: 08/23/2022

Who covered this study?

MedPageToday

POLO Will Change Practice in Pancreatic Cancer This article rates 4.0 out of 5 stars

Bloomberg Weekly

AstraZeneca's Lynparza Slows Spread of Rare Pancreatic Cancer This article rates 2.0 out of 5 stars

How we rated the media

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