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Lynch SyndromeOCCPINCT01850654

Ohio Colorectal Cancer Prevention Initiative

A study testing LS tumor screening, Genetic testing and Genetic Counseling in people with Lynch Syndrome and Colorectal Cancer, run by Ohio State University Comprehensive Cancer Center at 49 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of the Ohio Colorectal Cancer Prevention Initiative (OCCPI) is to reduce morbidity and mortality due to colorectal cancer (CRC) in the state of Ohio. By identifying individuals at high-risk for CRC (genetically predisposed) and providing screening recommendations for cancer risk reduction, the OCCPI will… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Lynch Syndrome, Colorectal Cancer
What is being tested?
LS tumor screening, Genetic testing and Genetic Counseling
Could I receive a placebo?
No, everyone receives an active treatment
How many people
3,470 participants
Where
49 sitesUnited States
Study dates
26 Dec 2012to 2 Jan 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Newly diagnosed with colorectal adenocarcinoma (all stages) and have a resection at any hospital in Ohio between 1/1/2013 and 12/31/2016.
  • For individuals who have neoadjuvant treatment and show a complete response at resection, the tumor screening will be attempted on their original biopsy (even if it occurred in 2012) as long as their resection occurred between 1/1/2013 and 12/31/2016.
  • Many individuals with stage IV CRC will not have a resection; therefore, the tumor screening will be attempted on their original colon biopsy as long as their primary diagnosis occurred between 1/1/2013 and 12/31/2016. If only metastatic CRC is available on a biopsy (liver or lymph node metastases), tumor screening will be attempted on the metastatic tissue.
  • Newly diagnosed with endometrial cancer (any histology except sarcoma) and have a resection between 1/1/2013 and 12/31/2016 at OSU only.
  • All at-risk relatives of the participants found to have LS.
  • First-degree relatives (parents, siblings and adult children ≥ 25 years of age) of the CRC participants who do not have LS.

Who cannot join

  • Prisoners.
  • Individuals who are under the age of 18.
  • Individuals must have a primary colorectal or endometrial cancer, not a recurrence of a previous colorectal or endometrial cancer.

Trial locations and contacts

49 sites in 1 country.

49 sites in 1 country

United States49 sites
  • Akron General Medical Center

    Akron, Ohio, 44109

  • Akron City/St. Thomas Hospital (Summa Health System)

    Akron, Ohio, 44309

  • Summa Barberton (Summa Health System)

    Barberton, Ohio, 44203

  • Mercy Clermont

    Batavia, Ohio

  • Mercy Medical Center

    Canton, Ohio, 44708

  • Aultman Hospital

    Canton, Ohio, 44710

  • Adena Health System

    Chillicothe, Ohio, 45601

  • The Christ Hospital

    Cincinnati, Ohio, 45219

  • Good Samaritan Hospital (TriHealth)

    Cincinnati, Ohio, 45220

  • Bethesda North Hospital (TriHealth)

    Cincinnati, Ohio, 45242

  • Mercy Anderson

    Cincinnati, Ohio

  • Mercy West

    Cincinnati, Ohio

  • The Jewish Hospital

    Cincinnati, Ohio

  • MetroHealth

    Cleveland, Ohio, 44109

  • Fairview Hospital

    Cleveland, Ohio, 44111

  • Cleveland Clinic

    Cleveland, Ohio, 44195

  • Mount Carmel East Hospital

    Columbus, Ohio, 43213

  • Riverside Methodist Hospital

    Columbus, Ohio, 43214

  • Grant Medical Center

    Columbus, Ohio, 43215

  • Mount Carmel West Hospital

    Columbus, Ohio, 43222

  • Doctors Hospital

    Columbus, Ohio, 43228

  • Summa Western Reserve (Summa Health System)

    Cuyahoga Falls, Ohio, 44223

  • Miami Valley Hospital

    Dayton, Ohio, 45409

  • Good Samaritan Hospital Dayton

    Dayton, Ohio, 45415

  • Kettering Medical Center

    Dayton, Ohio, 45429

  • Wright-Patterson Medical Center

    Dayton, Ohio, 45433

  • Grady Memorial Hospital

    Delaware, Ohio, 43015

  • Mercy Fairfield

    Fairfield, Ohio

  • Blanchard Valley Health System

    Findlay, Ohio, 45840

  • Wayne Healthcare

    Greenville, Ohio, 45331

  • Fairfield Medical Center

    Lancaster, Ohio, 43130

  • St. Rita's Medical Center

    Lima, Ohio, 45801

  • Marietta Memorial Hospital

    Marietta, Ohio, 45750

  • Marion General Hospital

    Marion, Ohio

  • St. Luke's Hospital (ProMedica)

    Maumee, Ohio, 43537

  • Toledo Clinic Cancer Center

    Maumee, Ohio

  • Hillcrest Hospital

    Mayfield Heights, Ohio, 44124

  • Atrium Medical Center

    Middletown, Ohio, 45005

  • Knox Community Hospital

    Mount Vernon, Ohio, 43050

  • Licking Memorial Hospital

    Newark, Ohio, 43055

  • Southern Ohio Medical Center

    Portsmouth, Ohio, 45648

  • Robinson Memorial (Summa Health System)

    Ravenna, Ohio, 44266

  • Springfield Regional Medical Center

    Springfield, Ohio, 45504

  • Flower Hospital (ProMedica Health System)

    Sylvania, Ohio, 43560

  • Toledo Hospital (Promedica Health System)

    Toledo, Ohio, 43606

  • Upper Valley Medical Center

    Troy, Ohio, 45373

  • South Pointe Hospital

    Warrensville Heights, Ohio

  • Mount Carmel St. Ann's Hospital

    Westerville, Ohio, 43081

  • Genesis Cancer Care Center (Genesis Healthcare System)

    Zanesville, Ohio, 43701

Other trials in United States

About this study

Official title: Ohio Colorectal Cancer Prevention Initiative: Universal Screening for Lynch Syndrome

The purpose of the Ohio Colorectal Cancer Prevention Initiative (OCCPI) is to reduce morbidity and mortality due to colorectal cancer (CRC) in the state of Ohio. By identifying individuals at high-risk for CRC (genetically predisposed) and providing screening recommendations for cancer risk reduction, the OCCPI will understand how to increase length of life and quality of life for those diagnosed with CRC in Ohio, as well as to better prevent CRC in others in Ohio.

Participants will have free tumor screening for Lynch syndrome, and may be eligible for free genetic testing and free genetic counseling as part of this study.

Read the detailed description

Lynch Syndrome:

Lynch syndrome (LS), previously known as "hereditary non-polyposis colorectal cancer", is a hereditary cancer syndrome that causes the majority of hereditary CRC and approximately 3% of all CRC. LS significantly increases the risk for an individual to develop CRC during their lifetime. Individuals with LS also have an increased risk to develop extracolonic cancers, including endometrial, gastric, ovarian, upper urinary tract, small bowel, biliary tract, CNS, and certain types of skin cancer. Tumor studies, including microsatellite instability (MSI) testing and immunohistochemical (IHC) analysis, provide information regarding characteristic features of LS-associated tumors and can help target genetic testing. Given the hereditary nature of this syndrome, screening all patients who are newly diagnosed with CRC for LS can identify additional individuals who are at high-risk of developing cancer.

Study Aims:

By developing a CRC research infrastructure within the state of Ohio, the OCCPI will achieve the following specific aims:

  • Establish and implement a statewide universal screening protocol for LS.
  • Elucidate the prevalence of hereditary CRC in Ohio.
  • Provide screening recommendations for high-risk individuals with CRC and their families, as well as local access to genetic counseling.
  • Create a CRC biorepository for future research on the etiology of CRC from the leftover samples of the CRC patients, as well as samples from their relatives.

With the successful implementation of the OCCPI, knowledge will be gained that will facilitate the adoption of a universal screening protocol for LS in Ohio and the creation of a statewide CRC biorepository to be used for additional studies on cancer risks, prevention, screening, treatment and survivorship.

Study Procedures for CRC and EC participants:

  • You will be asked to donate 2-3 tablespoons of blood.
  • A small piece of your colorectal or endometrial tumor will be obtained from the hospital where you had your surgery.
  • You will be asked to contribute your leftover samples (tumor and blood) to the OCCPI biorepository (sample bank) for help with future research. Additionally, CRC participants will be asked to donate a saliva sample to the OCCPI biorepository. The samples will be kept securely in a lab at OSU. Before your samples can be used for research, the people doing the research must get specific approval from the OCCPI Steering Committee and possibly the Institutional Review Board (IRB) of OSU. The IRB is responsible for protecting the participants involved in research studies and making sure all research is done in a safe and ethical manner.
  • You will be asked to complete a questionnaire which will ask about your age, medical history, family history, lifestyle factors and environmental exposures. It should take about one hour to complete the questionnaire and you can complete it from home.
  • We will test your tumor for features of LS (MSI, IHC, methylation).
  • For CRC patients: if your tumor shows features of LS OR you were diagnosed under age 50 OR you have a family history of CRC or endometrial cancer OR you have synchronous or metachronous CRC or endometrial cancer, we will test your blood for the genes that cause LS, as well as other genes that can cause hereditary cancer.
  • For endometrial cancer patients: if your tumor shows features of LS, we will test your blood for the genes that cause LS, as well as other genes that can cause hereditary cancer.
  • Some patients may have tumor genetic testing.
  • If you are found to have LS or another type of hereditary cancer, you will be offered free genetic counseling.
  • If you are found to have LS, your at-risk relatives will be offered free genetic counseling and genetic testing.

Study Procedures for first-degree relatives (FDR) of the CRC participants:

The FDRs of all of the CRC study participants will be given the opportunity to contribute to the biorepository for future research.

  • Family Member Consent for Contact forms will be provided to the CRC participant at the time of their enrollment for them to distribute to all of their FDRs (parents, siblings and adult children ≥ 25 years). The FDRs will mail the signed form to OSU.
  • After obtaining permission to contact the FDRs, OSU will mail them the biorepository consent form and saliva kit to return to the OCCPI biorepository.
  • The FDRs of the CRC study participants will also be invited to complete the baseline questionnaire.

Length of study:

  • The LS tumor screening portion of the OCCPI will take 1-4 months.
  • If applicable, genetic testing results should be ready in an additional 3-6 months.
  • Overall, your participation in the LS screening portion of the OCCPI is expected to take about 1 year. Most of this time will be spent waiting for results. Your active involvement will take about 15 minutes on the day that you provide consent and about 60 minutes when you complete the questionnaire from home.
Being tested
LS tumor screening, Genetic testing, Genetic Counseling, Biorepository, Questionnaire
Keywords
colorectal cancer, colon cancer, rectal cancer, endometrial cancer, Lynch syndrome, Ohio colon cancer study, OSU colon study
Medical subject headings
Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal Neoplasms, Colonic Neoplasms, Rectal Neoplasms, Endometrial Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LS tumor screeningGenetic

    Also called MSI, IHC, Methylation

    All participants with CRC or EC will have LS tumor screening (MSI, IHC, methylation if applicable).

  • Genetic testingGenetic

    Next-generation sequencing panel of several genes that increase the risk for hereditary cancers including the LS genes (MLH1, MSH2, MSH6, PMS2, EPCAM), polyposis genes (MUTYH, APC), and others.

    The following study participants will have free genetic testing:

    • CRC and EC study participants with unmethylated MSI-high (MSI-H) tumors
    • CRC and EC study participants with microsatellite stable (MSS) or MSI-low (MSI-L) tumors who have abnormal IHC results and they do not have methylation of the MLH1 promoter
    • CRC study participants diagnosed with CRC <50 years, regardless of tumor studies or family history
    • CRC study participants diagnosed with CRC ≥ 50 years with a FDR with CRC or EC OR synchronous or metachronous CRC or EC throughout their life, regardless of tumor studies.

    At-risk relatives of the individuals found to have LS are eligible for free single site genetic testing.

  • Genetic CounselingBehavioural

    The participants found to have LS or another type of hereditary cancer will have free genetic counseling.

    At-risk relatives of the individuals found to have LS are eligible for free genetic counseling.

  • BiorepositoryOther

    The biorepository is an optional part of the OCCPI. CRC and EC participants will contribute leftover tumor and blood samples, as well as a saliva sample. FDR of the CRC participants will contribute a saliva sample. The at-risk relatives of those found to have LS will contribute blood and saliva samples.

  • QuestionnaireBehavioural

Study groups in NCT01850654
Study groupRoleWhat they receive
ProbandsOtherParticipants with colorectal or endometrial cancer.
Receives: Genetic: LS tumor screening; Genetic: Genetic testing; Behavioral: Genetic Counseling; Other: Biorepository; Behavioral: Questionnaire
First-degree relatives of the participants with CRCOtherThe first-degree relatives of the CRC probands (participants with colorectal cancer).
Receives: Other: Biorepository; Behavioral: Questionnaire
At-risk relativesOtherThe relatives of the participants found to have Lynch syndrome.
Receives: Genetic: Genetic testing; Behavioral: Genetic Counseling; Other: Biorepository; Behavioral: Questionnaire

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Determine the Incidence of Hereditary Cancer Syndromes among Newly Diagnosed Colorectal Cancer Patients

    Through tumor testing for Lynch syndrome and follow-up genetic testing for all patients with abnormal tumor testing and select patients with normal tumor testing (those diagnosed under age 50 and those at or over age 50 with a first degree relative with colorectal or endometrial cancer or synchronous or metachronous colon or endometrial cancer).

    Measured: 36 months (initial assessment)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 May 2013 (estimated)
  2. Study start26 Dec 2012
  3. Primary completion2 Jan 2018
  4. Study completion2 Jan 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
3,470 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01850654
Sponsor's protocol ID
OSU-12170
Acronym
OCCPI
Status last verified
Jun 2018
First submitted
3 May 2013
Last updated
28 Jun 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med. 2005 May 5;352(18):1851-60. doi: 10.1056/NEJMoa043146.

    PubMed 15872200
  • Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Clendenning M, Sotamaa K, Prior T, Westman JA, Panescu J, Fix D, Lockman J, LaJeunesse J, Comeras I, de la Chapelle A. Feasibility of screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol. 2008 Dec 10;26(35):5783-8. doi: 10.1200/JCO.2008.17.5950. Epub 2008 Sep 22.

    PubMed 18809606
  • Palomaki GE, McClain MR, Melillo S, Hampel HL, Thibodeau SN. EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome. Genet Med. 2009 Jan;11(1):42-65. doi: 10.1097/GIM.0b013e31818fa2db. No abstract available.

    PubMed 19125127
  • Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group. Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. Genet Med. 2009 Jan;11(1):35-41. doi: 10.1097/GIM.0b013e31818fa2ff.

    PubMed 19125126

Questions about this trial

What is this clinical trial studying?

A study testing LS tumor screening, Genetic testing and Genetic Counseling in people with Lynch Syndrome and Colorectal Cancer, run by Ohio State University Comprehensive Cancer Center at 49 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Jun 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 49 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Determine the Incidence of Hereditary Cancer Syndromes among Newly Diagnosed Colorectal Cancer Patients (time frame: 36 months (initial assessment)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01850654, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jun 2018.

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