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Project Report
Peer-Review Record

Project COALESCE—An Example of Academic Institutions as Conveners of Community-Clinic Partnerships to Improve Cancer Screening Access

Int. J. Environ. Res. Public Health 2022, 19(2), 957; https://doi.org/10.3390/ijerph19020957
by Katherine Y. Tossas 1,2,3,*, Savannah Reitzel 1, Katelyn Schifano 3, Charlotte Garrett 3, Kathy Hurt 3, Michelle Rosado 3, Robert A. Winn 3 and Maria D. Thomson 1,3
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Reviewer 3: Anonymous
Int. J. Environ. Res. Public Health 2022, 19(2), 957; https://doi.org/10.3390/ijerph19020957
Submission received: 30 November 2021 / Revised: 5 January 2022 / Accepted: 7 January 2022 / Published: 15 January 2022
(This article belongs to the Special Issue Cancer Health Disparities and Public Health)

Round 1

Reviewer 1 Report

It is a very interesting study presenting crucial data regarding disparities for early cancer screening among Caucasians and non-Caucasians residing in Virginia. Studies like this are extremely needed especially due to the current pandemic has shown how significant is health inequality in the US.

Nevertheless, the article should be improved. Firstly, the article should present some data why only a small number of federal healthcare centres have decided to participate in this program, i.e., what motivated them to take part in this research project. Secondly, the clinical aspects of screening for CRC and CCa should be presented more. Thirdly, the assumption for selection bias should be made and described. In particular, some patients could primarily attend a local GP or a family doctor who is capable of organising minimally invasive screening procedures for CRC and CCa. It is not novel, that sometimes local GPs make wrong decisions due to lack of experience, absence of equipment etc. which will overall lead to misdiagnosis and cancer progression. By the time the patient reaches the federal healthcare centre, the cancer has already progressed which means that screening programs failed. Please elaborate methods how the selection bias was mitigated in this study.

 

Major comments

  • Perhaps it will be great to see the medical data regarding methods for screening for CCa and CRC. Whether it was less invasive (cheaper) Pap smear and FOBT or more invasive (expensive) colposcopy with colonoscopy. The cost, sensitivity and specificity of abovementioned diagnostic methods is different, and it will be great to read some insights regarding which methods are preferred to be used in different racial groups.
  • The percentage of Caucasians and non-Caucasian physicians working within the same clinical settings where the examined participants were studies should be elucidated.
  • 5 – regarding self-reported race-related issues. The data regarding mental status and socioeconomic level of those patients should be also provided. Sometimes those factors can impact to patient’s misunderstanding, absence of rapport and as a result to race-related issues.

 

Minor comments

  • Such words like “anecdotally” should not be used in the Journal’s Article.

Author Response

Reviewer 1: 

It is a very interesting study presenting crucial data regarding disparities for early cancer screening among 
Caucasians and non-Caucasians residing in Virginia. Studies like this are extremely needed especially due 
to the current pandemic has shown how significant is health inequality in the US. 

Author response: Thank you! 

Nevertheless, the article should be improved. Firstly, the article should present some data why only a small 
number of federal healthcare centres have decided to participate in this program, i.e., what motivated them 
to take part in this research project. 

 
Author response: The small number of participating FQHCs reflects the pilot nature of the project, rather 
than non-participation (opt-out) of facilities. Only five FQHCs were recruited. As stated in the manuscript, 
the 5 FQHCs were chosen based on “2018 HRSA data to identify five FQHCs in Virginia with CRC and CCa 
screening rates well below the state’s average (70% and 84% respectively) and the Healthy People 2030 
goals for these cancers (74% and 84% respectively). We ensured these FQHCs minimally represented or 
surpassed the racial and ethnic (19% Black, 10% Latinx) and geographic (25% rural) diversity of the state” 

Secondly, the clinical aspects of screening for CRC and CCa should be presented more. 

Author response: We have added the following sentence to the bottom of the first paragraph in the 
introduction section (line 48) to clarify the types of screenings done for each of these cancers: “Yet, 
prevention and early detection of these cancers is possible through screenings that detect and/or remove 
pre-cancerous lesions (Papanicolaou for CCa and stool-based (i.e., FIT or FOBT) or visual (structural) 
exams (i.e., colonoscopy, flexible sigmoidoscopy) for CRC). 

Thirdly, the assumption for selection bias should be made and described. In particular, some patients could 
primarily attend a local GP or a family doctor who is capable of organising minimally invasive screening 
procedures for CRC and CCa. It is not novel, that sometimes local GPs make wrong decisions due to lack of 
experience, absence of equipment etc. which will overall lead to misdiagnosis and cancer progression. By 
the time the patient reaches the federal healthcare centre, the cancer has already progressed which means 
that screening programs failed. Please elaborate methods how the selection bias was mitigated in this 
study. 

Author response: Federally Qualified Health Centers in the United States provide primary care to patients 
in the community regardless of their ability to pay. They are not referral sites, as suggested by the 
reviewer’s comment. Their federal designation (provided by the Health Resources and Services 
Administration, HRSA) means they receive additional federal dollars to support care provision regardless 
of insurance status or finances. Therefore, FQHCs are more likely to serve publicly insured, uninsured, 
underinsured or uninsurable (i.e., non-US citizens) individuals. We have added a sentence to the end of the 
last paragraph in the introduction clarifying what is an FQHC: “FQHCs are community-based clinics that 
receive funds from the Health Resources and Services Administration (HRSA) to provide primary care 
regardless of a patient’s ability to pay.” 

Reviewer 1 Major comments: 

Perhaps it will be great to see the medical data regarding methods for screening for CCa and CRC. Whether 
it was less invasive (cheaper) Pap smear and FOBT or more invasive (expensive) colposcopy with 
colonoscopy. The cost, sensitivity and specificity of abovementioned diagnostic methods is different, and it 
will be great to read some insights regarding which methods are preferred to be used in different racial 
groups. 

 

Author response: While the cost, sensitivity, specificity and differential uptake by racial group are beyond 
the scope of this process manuscript, we added under “FQHC Baseline Data – Updated for Participating 
Clinics” some verbiage to address the type of testing available at the participating FQHCs, as well as 
proportion of providers able to perform these screenings on-site as follows: “They reported employing 170 

 
non-clinical staff, 103 nurses, and 68 providers, a majority (82% of providers) of which performed on-site 
Pap screening for CCa, all provided stool cards (predominantly Fecal Immunochemical Test, FIT cards) for 
CRC. 

 

The percentage of Caucasians and non-Caucasian physicians working within the same clinical settings 
where the examined participants were studies should be elucidated. 

 

Author response: We added a sentence to report provider race/ethnicity data for the 2 clinics that 
reported such data as follows: “FQHC Baseline Data – Updated for Participating Clinics”: “Of two clinics who 
reported the racial/ethnic composition of their providers, the clinics with the second and third largest 
proportion of nL-Black patient population (62% and 44% nL-Blacks) reported that 0% and 13% of their 
providers respectively identified as nL-Blacks.” 

 

The data regarding mental status and socioeconomic level of those patients should be also provided. 
Sometimes those factors can impact to patient’s misunderstanding, absence of rapport and as a result to 
race-related issues. 

 

Author response: While we agree with the reviewer that these individual-level factors may correlate with 
screening uptake, such information is beyond the scope of this manuscript, which is intended to describe 
the development process for the initiative. Additionally, mental health status might not be routinely 
collected for all patients, as well as socioeconomic level, beyond the proxies of insurance status, education, 
and perhaps the patient’s address. 

 

Minor comments: Such words like “anecdotally” should not be used in the Journal’s Article. 

 

Author response: The word “anecdotally” was used to refer to anecdotal evidence, which is qualitative 
data. However, we appreciate the reviewer’s feedback and have removed the word, as we had included the 
stated narrative in Box 1. 

Reviewer 2 Report

Dear authors, please find below some suggestions:

2.7. Data analysis

Line 218: authors report methods to summarize and analyze quantitative data but in results section there are not these information (Student t-test and what as descriptive index? Mean and sd or other descriptive statistics?).

Pearson Chi square test is used for categorical variables; with proportional variables the authors mean proportion? Is alpha at 0.05 the statistical significance threshold? Which software was used to perform data analysis?

  1. Results

Line 227: authors stated that FQHCs were “more likely”.. if these results refer to Chi-square test is not appropriate to verify that one condition is more likely but it would be correct to describe data, this result shows that in FQHCs group the proportion of people under 65 years old was slightly higher compare to non-participating FQHCs (74% vs 60%, p=0.01).

Line 233: why is there a bibliographic citation in results section?

3.5 section: the description of the results is not clear, especially about figure 1, authors state that the comparison is between FQHCs respondents and community organization but in x-axis of the graph there are stress conditions. As stated above, terms “more likely” is not appropriate for this type of analysis and test, these results show only the distribution of two variables (from a bivariate frequency distribution table).

Author Response

Reviewer 2: 

Line 218: authors report methods to summarize and analyze quantitative data but in results section 
there are not these information (Student t-test and what as descriptive index? Mean and sd or other 
descriptive statistics?). Pearson Chi square test is used for categorical variables; with proportional 
variables the authors mean proportion? Is alpha at 0.05 the statistical significance threshold? 
Which software was used to perform data analysis? 

Author response: We have clarified under the methods section of this process paper that “As data 
collection is ongoing, herein we provide the initial, univariate analysis of baseline data for year one 
of the project.” We also added the use of StataIC 13 software for quantitative analysis. 

 
Line 227: authors stated that FQHCs were “more likely”.. if these results refer to Chi-square test is 
not appropriate to verify that one condition is more likely but it would be correct to describe data, 
this result shows that in FQHCs group the proportion of people under 65 years old was slightly 
higher compare to non-participating FQHCs (74% vs 60%, p=0.01). 

Author response: We thank the reviewer for this statement. We have corrected to state “served a 
higher proportion of patients that were…” 

Line 233: why is there a bibliographic citation in results section? 

Author response: The citation refers the reader to the source for the stated Healthy People 2030 
goals. 

3.5 section: the description of the results is not clear, especially about figure 1, authors state that 
the comparison is between FQHCs respondents and community organization but in x-axis of the 
graph there are stress conditions. As stated above, terms “more likely” is not appropriate for this 
type of analysis and test, these results show only the distribution of two variables (from a bivariate 
frequency distribution table). 

Author response: We thank the reviewer for their comments. For figure one, the comparison is 
indeed between the FQHCs and the community organizations, represented by bars in two colors 
(orange and blue, respectively). The graph reports these three bars across three domains 
measured: cultural, individual, and institutional. While we could substitute the graph for the one 
below, the authors believe it would be simpler for the readers to keep the results grouped by 
domain on the X axis, rather than by type of organization (community organization versus FQHC). 

 

Author Response File: Author Response.pdf

Reviewer 3 Report

This is an interesting contribution addressing a relevant issue on healthcare access equality accross a same country. Similar concers are observed worlwide among different communities within a single country, e.g, elderly, immigrants, or people living in large innercities vs those living in suburban areas or isolated in mountains or field areas.

With regards to that, the COALESCE projet looks suitable for publication. It will retain attention of many readers.

The submission is however not very easy to read, since the are no tables and only one figure. The manuscript may be substantially improved while adding a few tables to highlights the result section

Author Response

Reviewer 3: 

 
This is an interesting contribution addressing a relevant issue on healthcare access equality accross a same 
country. Similar concers are observed worlwide among different communities within a single country, e.g, 
elderly, immigrants, or people living in large innercities vs those living in suburban areas or isolated in 
mountains or field areas. 

Author response: Tbank you! 

With regards to that, the COALESCE projet looks suitable for publication. It will retain attention of many 
readers. The submission is however not very easy to read, since the are no tables and only one figure. The 
manuscript may be substantially improved while adding a few tables to highlights the result section 

Author response: We have added an additional table (Table 1) to better describe the HRSA data “FQHC 
Baseline Data – HRSA, 2019” 

Round 2

Reviewer 1 Report

I believe that authors have responded to all my previous comments and the manuscript is ready for publication.

Author Response

We kindly thank the reviewer for taking the time to review our manuscript. Your comments have certainly made our manuscript better. 

Reviewer 2 Report

Dears authors, thanks for the changes you have made in the manuscript.

Some minor suggestions:

  • Line 219: please specify that alpha at 0.05 is the statistical significance threshold
  • Figure 1 shows distribution of community and FQHC stratifying by Cultural, individual and institutional subgroups. Is it correct that the two bars do not reach 100%? Lines 349,350 : the terms “more likely” are not appropriate for this type of test, these results show only the distribution of two variables (please modify it).

Author Response

We kindly thank the reviewer for taking the time to review our manuscript once again. Your comments continue to improve our manuscript.  

  • Line 219: please specify that alpha at 0.05 is the statistical significance threshold - RESPONSE: I have added verbiage to clarify that alpha 0.05 is the statistical significance threshold. 
  • Figure 1 shows distribution of community and FQHC stratifying by Cultural, individual and institutional subgroups. Is it correct that the two bars do not reach 100%? RESPONSE: No. The figure only depicts those from either the community organization or the FQHC that reported experiencing either cultural, individual or institutional race-related stress. Therefore, the bars shown should not total 100%. For example, for experiences of cultural race-related stress from the community organization (N=22), 75% reported having such experiences, thus 25% (not shown) did NOT report having those experiences. For simplicity, only the affirmative response is shown. We hope this clarifies for the reviewer. 
  • Lines 349,350 : the terms “more likely” are not appropriate for this type of test, these results show only the distribution of two variables (please modify it). RESPONSE: The language has been changed to specify that "proportionately more respondents from... reported xyz". We hope this change is satisfactory to the reviewer.
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