Integrating Tobacco Treatment Into Cancer Care: A Randomized Controlled Comparative Effectiveness Trial

Smoking Cessation Clinical Trial

Official title:

Integrating Tobacco Treatment Into Cancer Care: A Randomized Controlled Comparative Effectiveness Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01871506
• Other study ID #: 2013P001036
• Secondary ID: 1R01CA166147-01A
• Status: Completed
• Phase: N/A
• Start date: September 2013
• Est. completion date: May 2018

Study information

• Verified date: August 2019
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There are currently over 11 million cancer survivors in the U.S. and survival rates are increasing. Unfortunately, 10-30% of cancer patients are current smokers at the time of diagnosis, and many of these patients have elevated socioeconomic, medical, and psychosocial vulnerabilities. Documented risks associated with continued smoking following cancer diagnosis include decreased survival time; increased complications from surgery, radiation, and chemotherapy; and increased risk of second primary tumors. U.S. Department of Health & Human Services Public Health Service evidence-based tobacco treatment guidelines exist but have not been integrated into the cancer setting. This is a tremendous missed opportunity to address a modifiable risk factor. In recognition of this treatment gap, the National Cancer Institute (NCI) sponsored a conference in 2009 to address how to increase the readiness and capacity for delivery of tobacco treatment in Cancer Centers. The American Society of Clinical Oncology (ASCO) recommends identification, advice, and counseling of all smokers by their second oncology visit as a core quality indicator; however, currently only half of patients report being asked about tobacco use.

Specific Aim: To conduct a randomized controlled comparative effectiveness trial of two strategies to promote smoking cessation in suspected or newly diagnosed cancer patients.

Study Design: A multi-site randomized controlled comparative effectiveness trial will enroll 295 current smokers with suspected or newly diagnosed melanoma, lymphoma, thoracic, breast, genitourinary, gastrointestinal, head and neck, or gynecologic cancer. Participants will be randomly assigned to receive Intensive Counseling (IC) or "Standard Care" (SC). Both groups will receive an initial motivational counseling session and 3 weekly follow-up counseling sessions with a tobacco treatment counselor, conducted in-person or by telephone. The IC arm has the option to also receive:

• Smoking Cessation Medication: Up to a 12-week supply of FDA approved smoking cessation medication (Varenicline, bupropion, or combination NRT) at no cost to the participant.

• Extended Counseling: An additional 4 biweekly and 3 monthly proactive counseling sessions with a tobacco treatment counselor (total of 11 counseling contacts).

All participants will complete 1 baseline and 2 follow-up surveys, at 3 and 6 months. Self-reported abstinence will be biochemically confirmed at 3 and 6 months.

Description:

Specific Aims

Aim 1: To compare the effectiveness of two tobacco treatments that are integrated into cancer care in producing tobacco abstinence at 6 months.

Aim 2: To explore: a) mechanisms through which treatment promotes abstinence; b) subpopulations in which abstinence is promoted; and c) which aspects of treatment promote abstinence.

Aim 3: To compare the incremental cost effectiveness (cost per quit) of two tobacco treatments.

Exploratory Aim: To identify the percentage and associated characteristics of smokers who 1) enroll in tobacco treatment and 2) adhere to tobacco treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 303
• Est. completion date: May 2018
• Est. primary completion date: May 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

INCLUSION CRITERIA:

Adult men and women may participate in this study if he/she meet the following requirements:

1. Current, new* patient at one of our three participating study sites: Massachusetts General Hospital (MGH) Cancer Center, Memorial Sloan Kettering Cancer Center (MSKCC), or Dana-Farber Cancer Institute (DFCI);

2. Currently with suspected or newly diagnosed cancer (thoracic, breast, genitourinary, gastrointestinal, head and neck, gynecologic, lymphoma, melanoma);

3. Has smoked a cigarette, even a puff, in the past 30 days;

4. Is willing to consider trying to quit smoking using counseling and/or smoking cessation medication;

5. Is English or Spanish speaking (MGH); English speaking (MSK; DFCI);

6. Has regular telephone access.

[*Patients will be considered "new" and eligible under the following conditions:

1. if they are attending approximately one of their first 4 visits or are within approximately 3 months of the initial visit date with their primary oncologist at the Massachusetts General Hospital (MGH) Cancer Center, Memorial Sloan Kettering Cancer Center (MSKCC), or Dana-Farber Cancer Institute (DFCI) for suspected or recently diagnosed cancer;

2. if they come to the MGH, MSKCC, or DFCI for a second opinion, the patient opts to receive their cancer treatment at any of these institutions;

3. if they have a past cancer diagnosis, they are currently faced with a local and distant recurrence of tumors;

4. if they have been treated previously for other types of cancer, they are currently faced with a new form of cancer.]

EXCLUSION CRITERIA:

In an effort to be as inclusive as possible, a patient will be excluded only if he/she:

1. Is NOT currently receiving or has no intentions to receive care at one of three participating cancer treatment centers: Massachusetts General Hospital Cancer Center, Memorial Sloan Kettering Cancer Center, or Dana-Farber Cancer Institute (DFCI);

2. Is currently psychiatrically unstable or otherwise unable to provide informed consent as determined by study investigators or oncology clinician;

3. Is not English or Spanish speaking;

4. Is medically ineligible (as determined by their treating physician);

5. Has insufficient comprehension/literacy.

ADDITIONAL INFORMATION:

Participant inclusion/exclusion is not based on use of smoking cessation medication -- he/she may decide not to use any smoking cessation medication and still participate in the study. Patients deemed ineligible will be referred to the state quit line.

Patients interested in participating in the study should contact the appropriate contact person, based on whether they are a current patient at the MGH, MSKCC, or DFCI.

Related Conditions & MeSH terms

• Smoking Cessation

Intervention

Behavioral:
• Standard Care (SC)
Initial counseling session: The initial counseling session will last approximately 45 minutes and will be conducted in-person or by phone by a tobacco treatment counselor. The session will be structured in a 5 As format and utilize Motivational Interviewing (MI) techniques. 3 Weekly Follow-up Counseling Sessions: SC Patients will be offered 3 weekly proactive follow-up sessions, concentrated on quitting and staying quit throughout cancer treatment. Medication advice: The tobacco counselor will advise SC subjects to use smoking cessation medication to assist with their quit. Smoking cessation medication will not be provided by the study free of cost for SC subjects.
• Intensive Counseling (IC)
The IC model includes all components of the SC as well as extended counseling support and up to 90 days of free FDA approved smoking cessation medication. Extended counseling support: Participants in the IC group will be offered the same initial 4 counseling sessions as the SC group as well as 4 additional proactive biweekly sessions and 3 monthly booster sessions. Smoking cessation medication: IC participants will be offered a 4-week supply of FDA-approved smoking cessation medication (varenicline, bupropion or nicotine replacement therapy) of their choice, with the option to renew the medication twice for up to 90 days of free medication. Participants are not required to take smoking cessation medication.

Locations

Country	Name	City	State
United States	Dana-Farber Cancer Institute	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	Memorial Sloan-Kettering Cancer Center	New York	New York

Sponsors (3)

Lead Sponsor	Collaborator
Massachusetts General Hospital	National Cancer Institute (NCI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Biochemically Verified 7-day Point Prevalence Tobacco Abstinence at 6 Months	Number of participants with 7-day point-prevalence tobacco abstinence at 6-month follow-up, assessed by biochemically confirmed saliva cotinine (<15 ng/ml76, 82) or <10 ppm expired air carbon monoxide (CO) for participants concurrently using NRT	6 months
Secondary	Number of Participants With Biochemically Verified 7-day Point Prevalence Tobacco Abstinence at 3 Months	Number of participants with7 -day point-prevalence tobacco abstinence at 3-month follow-up, assessed by biochemically confirmed saliva cotinine (<15 ng/ml76, 82) or <10 ppm expired air carbon monoxide (CO) for participants concurrently using NRT	3 months
Secondary	Number of Participants With Continuous Tobacco Abstinence	Number of Participants with Continuous tobacco abstinence (between quit and follow-up) at 3 & 6 months	3 months to 6 months
Secondary	Number of Participants With Sustained Tobacco Abstinence	Number of Participants with Biochemically confirmed repeated point prevalence abstinence at 3 & 6 months	6 months
Secondary	Number of Participants With Self-reported 7-day Point Prevalence.	Number of Participants with Self-reported smoking abstinence of at least 7 days	6 months
Secondary	The Number of IT Participants Who Used Smoking Cessation Pharmacotherapy	The number of IT participants who used 1) smoking cessation pharmacotherapy (Y/N dispensed) 2) smoking cessation counseling (Y/N), 3) 1-2 4-week refills, 4) took 1-3 monthly booster sessions.	Treatment Initiation to 6 month follow-up
Secondary	The Number of IT Participants Who Used Smoking Cessation Counseling	The number of intervention participants who used smoking cessation counseling during the study (Y/N)	Treatment Initiation to 6 Month Follow-up
Secondary	The Number of IT Participants Who Took 1-2 4-week Refills	The number of intervention participants who took 1-2 4-week refills of smoking cessation medication	Treatment Initiation to 6 Month Follow-up
Secondary	The Number of IT Participants Who Took 1-3 Monthly Booster Sessions	The number of IT participants who took 1-3 monthly booster sessions of smoking cessation counseling	Treatment Initiation to 6 Month Follow-up
Secondary	Cost-effectiveness	The cost of the standard of care treatment and the cost of the intensive treatment.	6 months