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. 2022 Jun 15;57(Suppl 2):222–234. doi: 10.1111/1475-6773.13996

Multilevel factors associated with inequities in multidisciplinary cancer consultation

Janeth I Sanchez 1,, Michelle Doose 2, Chris Zeruto 3, Veronica Chollette 1, Natalie Gasca 4, Dana Verhoeven 1, Sallie J Weaver 1
PMCID: PMC9670237  PMID: 35491756

Abstract

Objective

To assess changes in the prevalence of multidisciplinary cancer consultations (MDCc) over the last decade and examine patient, surgeon, hospital, and neighborhood factors associated with receipt of MDCc among individuals diagnosed with cancer.

Data Source

Surveillance, Epidemiology and End Results (SEER)–Medicare data from 2006 to 2016.

Study Design

We used time‐series analysis to assess change in MDCc prevalence from 2007 to 2015. We also conducted multilevel logistic regression with random surgeon‐ and hospital‐level effects to assess associations between patient, surgeon, neighborhood, and health care organization‐level factors and receipt of MDCc during the cancer treatment planning phase, defined as the 2 months following cancer diagnosis.

Data Collection/Extraction Methods

We identified Medicare beneficiaries >65 years of age with surgically resected breast, colorectal (CRC), or non‐small cell lung cancer (NSCLC) stages I–III (n = 103,250).

Principal Findings

From 2007 to 2015, the prevalence of MDCc increased from 35.0% to 61.2%. Overall, MDCc was most common among patients with breast cancer compared to CRC and NSCLC. Cancer patients who were Black, had comorbidities, had dual Medicare‐Medicaid coverage, were residing in rural areas or in areas with higher Black and Hispanic neighborhood composition were significantly less likely to have received MDCc. Patients receiving surgery at disproportionate payment‐sharing or rural‐designated hospitals had 2% (95% CI: −3.55, 0.58) and 17.6% (95% CI: −21.45, 13.70), respectively, less probability of receiving MDCc. Surgeon‐ and hospital‐level effects accounted for 15% of the variance in receipt of MDCc.

Conclusions

The practice of MDCc has increased over the last decade, but significant geographical and health care organizational barriers continue to impede equitable access to and delivery of quality care across cancer patient populations. Multilevel and multicomponent interventions that target care coordination, health system, and policy changes may enhance equitable access to and receipt of MDCc.

Keywords: health care delivery, inequities, multidisciplinary cancer care, multilevel


What is known on this topic

  • Multidisciplinary cancer consultations (MDCc) are associated with delivery of timely, guideline‐concordant cancer care.

  • There are persistent disparities in access to cancer care among minority and medically underserved populations.

  • Multilevel contextual measures of equitable access to MDCc have not been previously assessed.

What this study adds

  • The prevalence of MDCc increased from 35.0% to 61.2% from 2007 to 2015 across breast, colorectal, and non‐small‐cell lung cancer patients, albeit unequally for all.

  • Cancer patients who are Black, dual Medicare–Medicaid covered, residing in neighborhoods with high minority composition, and receiving surgery in rural‐designated and disproportionate sharing hospitals are significantly less likely to receive MDCc.

  • Using multilevel analyses, we found that 15% of the variation in receipt of MDCc was attributed to surgeons and hospitals.

1. INTRODUCTION

In 2021, many of the 1.8 million individuals diagnosed with cancer would have received multimodal treatments from various oncology specialists. Multidisciplinary care consultations (MDCc) refer to an array of care delivery approaches in which patients see or have their case evaluated by multiple health professionals, including medical oncologists, surgeons, and/or radiation oncologists, to identify treatment options, formulate optimized treatment plans, and initiate treatment. 1 Evidence from systematic reviews conducted over the last decade indicate that MDCc is associated with improvements in receipt of guideline‐concordant treatment, diagnostic accuracy, staging completeness, surgical techniques, and timeliness of care, with most studies focusing on lung/thoracic, head/neck, or gastrointestinal cancers. 2 , 3 , 4 , 5 , 6 , 7 , 8 MDCc has also been studied in the context of breast and prostate cancers given evolutions in multimodal management of these cancers. 8 , 9 Despite this research, the field lacks population‐based studies examining MDCc prevalence among some of the most commonly diagnosed cancers with the highest mortality rates such as breast, colorectal, and lung cancers.

Although clinical practice norms suggest MDCc is most common for patients with advanced cancers or complex cases, the use of models for delivering MDCc (e.g., multidisciplinary clinics) has grown across clinically diverse cancer populations as treatment options expand and patients seek consultations with multiple specialists to develop treatment plans. Even for patients with early stage cancers who may be recommended to receive surgery alone, engaging with a medical oncologist or radiation oncologist early in treatment planning may improve shared clinical decision making, care coordination, and receipt of timely, guideline‐concordant care. 3 , 9 , 10 , 11 , 12 , 13 , 14 , 15 However, although MDCc has been encouraged for nearly two decades, 16 it remains unclear whether MDCc is equitably delivered and/or received across diverse cancer patient populations.

Disparities in cancer outcomes experienced by racial and ethnic minorities and medically underserved populations (e.g., socioeconomically disadvantaged and rural populations) may arise from multilevel domains of influence including structural discrimination and system‐level barriers, such as limited availability of quality cancer care. 17 , 18 Limited prior research examining variation in receipt of MDCc suggests that patients who identify as Black, older, unmarried, and with comorbidities are less likely to receive MDCc. 9 , 10 , 13 , 14 Geographically, cancer patients residing in communities with large racial and ethnically minoritized populations, that are rural, and with higher poverty rates are more likely to experience limited access to cancer specialists and worse cancer outcomes. 13 , 19 Differences in the delivery of cancer care by physician specialty and health care settings has also been identified. Among Surveillance Epidemiology and Ends Results (SEER)‐Medicare beneficiaries with breast or colorectal cancer, 20% of cancer treatment variations were explained by factors beyond the patient level (i.e., between‐physician differences). 20 Additionally, among cancer patients receiving surgery, there is substantial between‐hospital variation in mortality and readmission rates with safety‐net hospitals, which often serve minority and medically underserved populations, having higher 90‐day readmission rates. 21 However, to our knowledge, no studies have concurrently examined patient, physician, hospital, and neighborhood factors associated with MDCc in a population‐based sample of patients with common high‐mortality cancers. 22 , 23 , 24 , 25

To address this gap, we used the SEER‐Medicare data to assess the prevalence of MDCc from 2007 to 2015, using a multilevel analysis to examine patient‐, neighborhood‐, surgeon‐, and hospital‐level factors associated with receipt of MDCc among Medicare beneficiaries with surgically resected (female) breast cancer, colorectal cancer (CRC), or non‐small‐cell lung cancer (NSCLC).

2. DATA AND METHODS

2.1. Data sources and study population

This retrospective population‐based cohort study used the SEER–Medicare linked data (2006–2016) to identify Medicare beneficiaries over 65 years of age with a pathologically staged (I, II, and III) single (female) breast cancer, CRC, or NSCLC as their first and only cancer. We identified patients who received surgical resection within 12 months after date of diagnosis, as confirmed by the first surgical claim for primary cancer (See Appendix S1). We excluded patients enrolled in a health maintenance organization or not enrolled in Medicare Parts A and B for at least 12 months before their cancer diagnosis and through study period, diagnosed at time of autopsy or death certificate, or died within 12 months from date of diagnosis, as we would not be able to fully capture MDCc claims. We also excluded patients missing month of diagnosis.

2.2. Measures

2.2.1. Outcome: Receipt of multidisciplinary cancer consultations (MDCc)

MDCc is operationalized as having encounters with two or more of the following oncology specialties within 2 months from diagnosis: surgery, medical oncology, and/or radiation oncology. Our approach aligns with Medicare claims guidelines and billing practices for physicians during the period of study. In the absence of specific guidelines for MDCc, the 2‐month time frame was chosen as it has been used as a quality indicator in other studies. 9 , 13 We also conducted sensitivity analyses using a 4‐month time frame. We secondarily assessed whether MDCc occurred on the same day.

We identified consultations with all oncology provider specialties using Carrier Claims with listed Current Procedural Terminology codes for patient encounters (See Appendix S1). We used National Provider Identifier information from these claims merged with American Medical Association (AMA) data to determine provider specialty. Provider specialty was ascertained using a hierarchical scheme using both primary and secondary specialty codes (See Appendix S1). 26 , 27

2.2.2. Multilevel predictors

Patient characteristics

Patient sociodemographic characteristics included age at diagnosis, race and ethnicity (non‐Hispanic [NH]‐Black, NH‐White, Hispanic, or Other), sex, marital status, and Medicare–Medicaid dual coverage status defined as being covered through a state buy‐in program at any point during study period (yes/no). Patient clinical characteristics included cancer type, staging, and number of comorbidities using the National Cancer Institute's (NCI's) comorbidity index. 28 Patient sociodemographic characteristics, including race and ethnicity, in the SEER‐Medicare database were obtained from the SEER cancer registries that collect data from various sources (e.g., administrative databases, patient intake forms, provider records, and imputation algorithms) and the Medicare database. 29 Per the SEER‐Medicare data use agreement, American Indian/Alaska Native, Asian, Pacific Islander, and unknown race or ethnicity were combined into a single “Other” category to protect confidentiality.

Neighborhood characteristics

Neighborhood characteristics included census‐tract‐level indices of racial and ethnic composition (e.g., percentage Black individuals, percentage Hispanic individuals), area deprivation, SEER registry geographic location, and rurality. Percent Black and Hispanic composition was categorized into quartiles based on the distribution of the study population within a census tract. Patient's zip code was linked to the Neighborhood Atlas's Area Deprivation Index (ADI) data to capture neighborhood socioeconomic disadvantage based on state‐level rankings. 30 SEER registry geographic location was categorized as Northeast, Midwest, Southwest, South, and West. Patient‐level zip codes were linked to the 2013 Rural–Urban Continuum Codes (RUCC) to obtain scores (1–3 classified as urban and 4–9 classified as rural). 31

Surgeon characteristics

For each surgeon, we identified surgical specialty (general, oncology, other), medical school graduation year (before 2000 or later), and sex (male, female). Individual provider information was obtained from the AMA data.

Hospital characteristics

Characteristics of the hospital where patients received their first surgery included NCI Cancer Center designation (yes/no), Commission on Cancer accreditation (yes/no), teaching status (yes/no), hospital type (non‐profit, private, government), rural hospital status (yes/no), and disproportionate share hospital (DSH) payment qualification (yes/no). Hospital characteristics were obtained from the NCI's SEER‐Medicare's data Hospital File. 32

2.2.3. Statistical analyses

To describe the study population, we reported frequencies and percentages of patients who received MDCc within 2 months from diagnosis over multiple days or on the same day of MDCc. Significant differences in the distribution of patients by MDCc (vs. no MDCc) and same‐day MDCc (vs. MDCc received over multiple days) were assessed using the Pearson Chi‐square test. Bivariate and multilevel mixed‐effects logistic regressions were performed to assess the associations between multilevel factors and MDCc with patients (Level 1) nested within surgeon (Level 2) and then clustered by the hospital where first surgery was performed (Level 3). Random intercepts were modeled for surgeons and hospitals to account for this clustering. We included the multilevel factors presented in Table 1 as fixed effects. These factors were identified a priori based on Andersen's Model of Healthcare Utilization 33 and prior research on MDCc. As measures of individual and neighborhood socioeconomic status, we assessed whether dual Medicare–Medicaid coverage and area deprivation, respectively, varied by race and ethnicity; these interaction terms were not significant on the basis of a Wald test and were excluded from the model. We conducted sensitivity analyses to assess the prevalence of MDCc by cancer type, stage, and receipt of MDCc within 4 months from diagnosis.

TABLE 1.

Characteristics of breast, colorectal, and non‐small‐cell lung cancer patients who received multidisciplinary cancer consultation (MDCc) and same‐day MDCc between 2007 and 2015

Overall Cohort (N = 103,250) MDCc (n = 58,017) p‐Value (MDC vs. no MDC) Same‐day MDCc (n = 6990) p‐Value (same day vs. not same day)
n % n % n %
Patient level
Age (Mean ± SD) 75.9 ± 4.0 74.8 ± 3.9 <0.001 74.1 ± 3.9 <0.001
Race and ethnicity <0.001 0.265
Non‐Hispanic White 86,394 83.7% 48,830 56.5% 5859 11.9%
Non‐Hispanic Black 6619 6.4% 3265 49.3% 405 12.3%
Hispanic 4832 4.7% 2744 56.8% 360 13.0%
Other 5405 5.2% 3036 56.2% 379 12.4%
Sex <0.001 <0.001
Male 19,848 19.2% 7593 38.3% 757 9.5%
Female 83,402 80.8% 50,282 60.3% 6246 12.4%
Marital status <0.001 0.026
Single 8291 8.4% 4310 52.0% 511 11.8%
Married 50,664 51.3% 30,000 59.2% 3735 12.3%
Other 39,831 40.3% 21,176 53.2% 2453 11.6%
Medicaid coverage <0.001 0.009
No 85,135 82.5% 49,680 58.4% 61,086 12.2%
Yes 18,115 17.5% 8195 45.2% 917 11.2%
Cancer type <0.001 <0.001
Breast 58,184 56.4% 41,643 71.6% 5614 13.4%
Colorectal 33,019 32.0% 11,575 35.1% 940 8.1%
Lung 12,047 11.7% 4657 38.7% 449 9.6%
Stage 0.292 <0.001
I 52,281 50.6% 29,407 56.3% 3710 12.6%
II 33,033 32.0% 18,499 56.0% 2187 11.7%
III 17,936 17.4% 9969 55.6% 1106 11.0%
Comorbidities <0.001 <0.001
0 51,921 51.0% 32,139 61.9% 4.051 12.5%
1 29,026 28.5% 15,818 54.5% 1855 11.7%
2 7201 7.1% 35,407 48.7% 403 11.4%
3+ 13,650 13.4% 5828 42.7% 619 10.5%
Neighborhood level
% Black composition <0.001 <0.001
Lower quartile 26,990 26.2% 15,771 58.4% 2061 13.0%
2nd quartile 26,444 25.6% 15,133 57.2% 1899 12.5%
3rd quartile 25,671 24.9% 14,295 55.7% 1704 11.9%
Highest quartile 24,054 23.3% 12,763 53.1% 1332 10.4%
% Hispanic composition <0.001 0.007
Lower quartile 25,159 24.4% 14,039 55.8% 1803 12.8%
Second quartile 26,445 25.6% 15,128 57.2% 1783 11.7%
Third quartile 26,340 25.5% 14,942 56.7% 1737 11.6%
Highest quartile 25,212 24.4% 13,709 54.4% 1673 12.1%
Area deprivation index <0.001 <0.001
Lowest quintile (lowest disadvantage) 24,544 25.2% 14,678 59.8% 1945 13.2%
2nd quintile 21,353 21.9% 12,264 57.4% 1381 11.2%
3rd quintile 19,181 19.7% 10,708 55.8% 1226 11.4%
4th quintile 17,646 18.1% 9575 54.3% 1141 11.9%
Highest quintile (most disadvantage) 14,747 15.1% 7604 51.6% 909 11.9%
Rurality (RUCC) <0.001 <0.001
Urban 86,377 83.7% 48,628 56.3% 5757 11.8%
Rural 16,861 16.3% 9239 54.8% 1244 13.4%
SEER region <0.001 <0.001
Northeast 22,173 21.5% 11,350 51.2% 1043 9.1%
Midwest 12,258 11.9% 6928 56.5% 1092 15.7%
Southwest 4256 4.1% 2656 62.4% 404 15.1%
South 26,178 25.4% 14,585 55.7% 1416 9.7%
West 38,385 37.2% 22,356 58.2% 3048 13.5%
Surgeon level
Surgeon specialty <0.001 <0.001
General 62,129 68.1% 39,129 63.0% 4649 11.8%
Oncology 9877 10.8% 6945 70.3% 986 14.1%
Other surgeon specialty 19,289 21.1% 7943 41.2% 699 8.8%
Surgeon graduation year 0.028 <0.001
Before 2000 82,386 90.2% 48,649 59.1% 5549 11.3%
2000 or later 8909 9.8% 5368 60.3% 785 14.5%
Surgeon sex <0.001 <0.001
Male 68,174 74.7% 37,398 54.9% 3799 10.1%
Female 23,121 25.3% 16,619 71.9% 2535 15.2%
Hospital level
Hospital type 0.019 <0.001
Non‐profit 69,539 75.8% 38,153 54.9% 4676 12.2%
Private 9532 10.4% 5340 56.0% 470 8.8%
Government 12,669 13.8% 6857 54.1% 773 11.2%
NCI designation 0.011 <0.001
None 89,095 93.6% 49,092 55.3% 5580 11.3%
Yes (clinical and/or comprehensive) 6047 6.4% 3230 53.4% 586 18.0%
CoC accreditation <0.001 0.004
No 41,061 43.2% 22,093 53.8% 2.709 12.2%
Yes 54,081 56.8% 30,229 55.9% 3457 11.4%
Teaching status <0.001 <0.001
No 42,810 46.7% 23,870 55.8% 2432 10.1%
Yes 48,925 53.3% 26,478 54.1% 3487 13.1%
Disproportionate share payment qualification 0.569 <0.001
No 18,050 19.7% 9876 54.7% 1332 13.4%
Yes 73,552 80.3% 40,417 55.0% 4583 11.3%
Rural primary status <0.001 <0.001
No 90,052 98.2% 49,728 55.2% 5883 11.8%
Yes 1683 1.8% 620 36.8% 36 5.8%

Abbreviations: CoC, Commission on Cancer; NCI, National Cancer Institute; RUCC, Rural–Urban Continuum Codes (2013); SD, standard deviation; SEER, Surveillance, Epidemiology, and End Results Program.

We calculated the variance inflation factor (mean VIF = 2.45) and could identify no significant evidence of multicollinearity between the multilevel factors in Table 1. Year of diagnosis was also included as a discrete covariate to account for the effect of calendar time on MDCc. We computed average marginal effects and report the (marginal) probability of receiving MDCc compared to the reference group, measured as the average changes in percentage (%) points, and 95% confidence intervals (CIs). To determine the variation in receipt of MDCc across surgeons and hospitals, we calculated the intraclass correlation (ICC) in a null (unadjusted) multilevel model without any patient, neighborhood, surgeon, and hospital factors and in the full model, which adjusted for all multilevel factors in Table 1. Statistical significance was assessed at the 0.05 level. All analyses were performed in STATA version 16.0 (STATA Corporation).

3. RESULTS

3.1. Patient and neighborhood characteristics

The study population included 103,250 patients with surgically resected breast, CRC, or NSCLC cancer from 2007 to 2015. Table 1 describes the characteristics of patients who received MDCc within 2 months from diagnosis. The mean patient age was 75 years. Significantly more Hispanic (56.8%), female (60.3%), and married (59.2%) patients, and patients without dual Medicare–Medicaid coverage (58.4%) received MDCc. Additionally, more patients without comorbidities (61.9%) received MDCc. Most patients residing in neighborhoods with a lower proportion of Black residents, lower area deprivation, urban areas, and in the Western part of the United States received MDCc. By cancer site, more breast cancer patients (71.6%) received MDCc than CRC (35.1%) or NSCLC patients (38.7%). Similar patient sociodemographic and clinical characteristics were observed for MDCc within 4 months from diagnosis and same‐day MDCc at both time periods.

3.2. Surgeon and hospital characteristics

There were 6456 unique surgeons and 1389 unique hospitals in this study. The number of patients per surgeon varied from 1 to 151 (median = 7.9), with 77.0% of the surgeons having at least two patients. The number of patients per hospital varied from 1 to 902 (median = 53.2), with only 13.7% of hospitals having only one patient. Most hospitals (78.8%) had at least two surgeons, and the number of surgeons per hospital varied from 1 to 73 (median = 7.2 surgeons per hospital). A higher proportion of patients who had their surgery performed by a surgeon specializing in oncology (70.3%), graduated from medical school after 2000 (60.3%), and by a female surgeon (71.9%) received MDCc. More patients who received surgery at a hospital that was private (56.0%), not NCI‐designated (55.3%), Commission on Cancer accredited (55.9%), and not designated as a rural hospital (55.2%) received MDCc.

3.3. Prevalence of MDCc

From 2007 to 2015, the prevalence of MDCc increased from 35.0% to 61.2%, while same‐day MDCc increased from 9.4% to 13.9% (p‐value <0.001) (Figure 1A). A total of 57,875 patients (56.1%) received MDCc, and of these, 12.0% received MDCc on the same day. Similar trends in prevalence of MDCc within 4 months from diagnosis were observed. Among patients who received MDCc, 91.8% had an encounter with a medical oncologist, 94.4% with a surgeon, and 49.1% with a radiation oncologist within 2 months of diagnosis. Consultation with both a medical oncologist and a surgeon was observed for 86.2% of patients with MDCc, while 35.7% of patients with MDCc had consultation with all three provider types. From 2007 to 2015, MDCc was highest among breast cancer patients overall and among stage II and III CRC or NSCLC patients compared to stage I (Figure 1B).

FIGURE 1.

FIGURE 1

Prevalence of multidisciplinary cancer consultation (MDCc) from 2007 to 2015. (A) Prevalence of MDCc and same‐day MDCc by year of cancer diagnosis. (B) Prevalence of MDCc by year of cancer diagnosis stratified by cancer type and stage. CRC, colorectal cancer; MDCc, multidisciplinary cancer consultation; NSCLC, non‐small‐cell lung cancer.

3.4. Factors associated with receipt of MDCc

Results from the adjusted multilevel analysis indicated that patients who were older, single, diagnosed with CRC or NSCLC, and with at least one comorbidity had a lower probability of receiving MDCc (Table 2). Compared to NH‐White patients, NH‐Black patients were 3.3% less likely to have received MDCc (95% CI: −4.78, −1.83), while Hispanic patients were 1.8% more likely to have received MDCc (95% CI: 0.18, 3.40). Late‐stage cancer was also significantly associated with a higher likelihood of receiving MDCc compared to patients diagnosed with stage I (stage II: 6.6%, 95% CI: 5.85, 7.31; stage III: 16.3%, 95% CI: 15.47, 17.15). Patients with dual Medicare–Medicaid coverage were 7.2% less likely to have received MDCc compared to patients without dual coverage (95% CI: −8.09, −6.22).

TABLE 2.

Average marginal effects of receiving multidisciplinary cancer consultation (MDCc) among Medicare beneficiaries with surgically resected cancer from 2007 to 2015

Unadjusted marginal effects Adjusted marginal effects a
Percentage (%) points (95% CI) Percentage (%) points (95% CI)
Patient level
Age −1.24 (−1.28, −1.20) −0.96 (−0.96, −0.86)
Race and ethnicity
Non‐Hispanic White Reference Reference
Non‐Hispanic Black −7.19 (−8.44, −5.94) −3.30 (−4.78, −1.83)
Hispanics 0.27 (−1.17, 1.70) 1.79 (0.18, 3.40)
Other −0.35 (−1.71, 1.01) 1.93 (0.34, 3.52)
Sex
Male Reference Reference
Female 22.03 (21.28, 22.79) 0.13 (−0.80, 1.07)
Marital status
Single Reference Reference
Married 7.23 (6.07, 8.39) 4.19 (2.96, 5.42)
Other 1.18 (0.00, 2.36) 1.13 (−0.11, 2.37)
Medicaid coverage
No Reference Reference
Yes −13.12 (−13.91, −12.32) −7.16 (−8.09, −6.22)
Cancer type
Breast Reference Reference
Colorectal −36.52 (−37.15, −35.88) −39.4 (−40.37, −38.36)
Lung −32.91 (−33.86, −31.97) −32.4 (−34.25, −30.59)
Stage
I Reference Reference
II −0.25 (−0.93, 0.44) 6.58 (5.85, 7.31)
III −0.67 (−1.51, 0.18) 16.31 (15.47, 17.15)
Comorbidities
0 Reference Reference
1 −7.40 (−8.11, −6.69) −2.05 (−2.80, −1.31)
2 −1.32 (−14.43, −11.97) −4.11 (−5.38, −2.83)
3+ −1.92 (−20.13, −18.27) −6.69 (−7.71, −5.67)
Neighborhood level
% Black composition
Lower quartile Reference Reference
Second quartile −1.20 (−2.04, −0.36) −0.19 (−1.11, 0.73)
Third quartile −2.77 (−3.62, −1.93) −0.19 (−1.18, 0.81)
Highest quartile −5.34 (−6.20, −4.47) −1.50 (−2.73, −0.28)
% Hispanic composition
Lower quartile Reference Reference
Second quartile 1.40 (0.55, 2.26) 0.24 (−0.72, 1.22)
Third quartile 0.93 (0.07, 1.78) 0.35 (−0.75, 1.44)
Highest quartile −1.43 (−2.29, −0.56) −1.38 (−2.71, −0.06)
Area deprivation index
Lowest quintile (lowest disadvantage) Reference Reference
Second quintile −2.37 (−3.27, −1.46) 0.65 (−0.324, 1.62)
Third quintile −3.98 (−4.91, −3.04) 0.41 (−0.6, 1.46)
Fourth quintile −5.54 (−6.50, −4.58) −0.05 (−1.18, 1.08)
Highest quintile (most disadvantage) −8.24 (−9.25, −7.23) −0.62 (−1.86, 0.63)
Rurality (RUCC)
Urban Reference Reference
Rural −1.50 (−2.32, −0.68) −1.75 (−3.00, −0.52)
SEER region
Northeast Reference Reference
Midwest 5.33 (4.23, 6.43) 8.13 (5.41, 10.85)
Southwest 11.22 (9.62, 12.81) 7.82 (4.32, 11.32)
South 4.53 (3.63, 5.42) 5.45 (3.08, 7.83)
West 7.05 (6.23, 7.88) 4.91 (2.70, 7.12)
Surgeon level
Surgeon specialty
General Reference Reference
Oncology 7.33 (6.36, 8.31) −0.55 (−2.32, 1.23)
Other surgeon specialty −21.80 (−22.59, −21.01) 0.71 (−0.58, 1.99)
Surgeon graduation year
Before 2000 Reference Reference
2000 or later 1.20 (0.13, 2.27) 0.79 (−0.62, 2.21)
Surgeon sex
Male Reference Reference
Female 17.02 (16.33, 17.71) 0.49 (−0.72, 1.70)
Hospital level
Hospital type
Non‐profit Reference Reference
Private 1.16 (0.09, 2.22) −1.29 (−3.17, 0.59)
Government −0.74 (−1.68, 0.20) −1.66 (−3.59, 0.26)
NCI designation
No Reference Reference
Yes −1.69 (−2.98, −0.39) −2.80 (−6.20, 0.60)
CoC accreditation
No Reference Reference
Yes 2.09 (1.45, 2.73) 2.90 (1.41, 4.40)
Teaching status
No Reference Reference
Yes −1.64 (2.28, −0.99) −0.44 (−1.84, 0.95)
Disproportionate share payment qualification
No Reference Reference
Yes 0.24 (−0.57, 1.05) −2.06 (−3.55, −0.58)
Rural primary status
No Reference Reference
Yes −18.38 (−20.71, −16.06) −17.57 (−21.45, −13.70)

Abbreviations: CI, Confidence Interval; CoC, Commission on Cancer; NCI, National Cancer Institute; RUCC, Rural–Urban Continuum Codes (2013); SEER, Surveillance, Epidemiology, and End Results Program.

a

Adjusted for age, race and ethnicity, sex, marital status, cancer type, cancer stage, comorbidities, percent Black and Hispanic neighborhood composition, area deprivation index, rurality, SEER region surgeon specialty, graduation year, sex, hospital type, NCI designation, Commission on Cancer accreditation, teaching status, disproportionate share payment qualification, rural primary status designation, year of diagnosis, and surgeon and hospital random effects.

Patients residing in neighborhoods with the highest Black (95% CI: −2.73, −0.28) or Hispanic (95% CI: −2.71, −0.06) composition had a 1.5% and 1.4% lower probability of receiving MDCc compared to patients residing in neighborhoods with lower (0%–25%) minority composition. Area deprivation was not significantly associated with receiving MDCc. Patients residing in rural areas had a 1.8% lower probability of receiving MDCc compared to patients residing in urban areas (95% CI: −3.00, −0.52).

Surgeon characteristics (i.e., specialty, sex, graduation year) were not significantly associated with MDC. However, patients receiving surgery at a Commission on Cancer accredited hospital had a significantly higher probability of receiving MDCc compared to patients receiving surgery at hospitals not accredited (2.9%, 95% CI: 1.41, 4.40). Receiving surgery at a hospital qualifying for DSH payment was associated with a 2.1% lower probability of receiving MDCc (95% CI: −3.55, −0.58), while patients receiving surgery at a rural primary status hospital had a 17.6% lower probability of receiving MDCc compared to patients receiving surgery at a non‐rural hospital (95% CI: −21.45, −13.70).

3.5. Variation in MDCc

In the null (unadjusted) multilevel model, the ICC for variation in receipt of MDCc attributed to the surgeon and hospital levels was 3.9% and 21.0%, respectively (Table 3). After accounting for patient, neighborhood, surgeon, and hospital characteristics, the variance in receipt of MDCc attributed to the hospital level reduced to 11.3% (95% CI: 10.3%, 12.4%).

TABLE 3.

Variance in receipt of multidisciplinary cancer consultations (MDCc) attributed to surgeon and hospital levels

Null (unadjusted) model Full (adjusted) model a
ICC 95%CI ICC 95%CI
Surgeon 3.9% (3.1%, 5.0%) 4.1% (3.3%, 5.1%)
Hospital 21.0% (19.9%, 22.2%) 11.3% (10.3%, 12.4%)
a

Adjusted for age, race and ethnicity, sex, marital status, cancer type, cancer stage, comorbidities, percent Black and Hispanic neighborhood composition, area deprivation index, rurality, SEER region surgeon specialty, graduation year, sex, hospital type, NCI‐designation, Commission on Cancer accreditation, teaching status, disproportionate share payment qualification, rural primary status designation, year of diagnosis.

4. DISCUSSION

In this study, MDCc after diagnosis almost doubled from 2007 to 2015, representing an uptake in an important cancer care quality metric. During this period, most of the 57,875 patients with MDCc (86.2%) saw both a surgeon and medical oncologist, while 35.7% had encounters with surgical, medical oncology, and radiation oncology providers. As expected, MDCc varied by cancer type and stage, with MDCc being most prevalent among breast cancer patients and adjusted analyses finding higher probability of MDCc among patients diagnosed with late‐stage cancers.

Consistent with prior studies, we found that patients who are older, single, and Black were less likely to receive MDCc even after accounting for neighborhood‐, surgeon‐, hospital‐, and other patient‐level factors. 10 , 13 , 14 , 34 The disparity between Black patients and NH‐White patients may be partly explained by differences in system‐level factors such as limited access to quality cancer care, mistrust of providers and health care systems, and/or lack of patient–provider communication. 35 , 36 Conversely, and similar to Simpson et al., 13 Hispanic patients in our study had a 1.8% higher probability of receiving MDCc compared to NH‐White patients, which may be associated with stronger cultural‐related advantages of residing in Hispanic enclaves (e.g., access to social networks, resilience, and the presence of patient navigators or promatoras to enhance care delivery). 37 , 38 However, we found that residing in neighborhoods with the highest Black or Hispanic composition was associated with a 1.4% and 1.5%, respectively, lower probability of receiving MDCc. 39 As a measure of racial composition, the percentage of residents who identify as Black or Hispanic within a specific geographical area is a potential reflection of neighborhood racial context where neighborhoods with higher proportions of racial and ethnic minoritized groups may experience structural and systemic barriers such as inadequate transportation, limited availability of quality cancer care resources, and increased exposures to stress, bias, and trauma that may impede utilization of cancer‐related health services. 39 Neighborhood characteristics not assessed in this study, such as social cohesion, housing‐pattern‐based segregation, neighborhood mobility and isolation, and other social risks, are also likely to play a role in access to and receipt of MDCc and should be assessed in future research. 40 , 41 , 42 , 43

We also found that the probability of receiving MDCc was 7.2% lower among patients with dual Medicare–Medicaid coverage. Patients with Medicaid coverage may experience access barriers to specialty care due to inadequate provider reimbursement and high administrative burden (e.g., preauthorization, payment delays, claim rejection) that may lead some specialists to limit their Medicaid patient panels. 44 These findings suggest opportunities for clinic‐, health‐system‐, and policy‐level interventions that facilitate access to high‐quality cancer care for patients with Medicaid, particularly for patients from racially and ethnically minoritized and medically underserved groups who are more likely to experience greater financial burden after a cancer diagnosis. 45 Such approaches may include value‐based care delivery models and aligning reimbursement with equity‐driven quality measures.

Additionally, we found a lower probability of receiving MDCc with increasing comorbidity. Newly diagnosed older adult cancer patients are likely to have concurrent conditions, such as heart disease and diabetes, and compounded disease severity that may adversely affect cancer treatment options and contribute to poorer survival. 46 Populations that experience health disparities, including racial and ethnic minorities, are more likely to have comorbid medical and mental health conditions compared to NH‐Whites. 47 While there is an important, growing body of research examining integration of geriatric assessment, multimorbidity, and multidisciplinary approaches for comprehensive care for older adults with cancer, 48 , 49 relatively limited evidence to date examines MDCc approaches among populations facing cancer and other comorbid conditions. 50 More research is needed to better understand the impact of MDCc on care management, coordination, and outcomes for patients with concurrent and competing health care needs throughout their cancer journey. Future research should evaluate effects of MDCc on important outcomes such as treatment‐related toxicities, recurrence, and progression‐free survival in these populations.

Geographically, rural patients had 1.8% lower probability of receiving MDCc compared to urban patients. Less than 15% of oncologists practice in rural settings, and rural cancer patients experience limited access to local clinical settings that provide cancer treatment and longer travel distances to oncology care. 51 , 52 , 53 Although only 12% of patients with MDCc had same‐day MDCc, a post hoc analysis (data not shown) indicated that rural patients with MDCc had a higher probability of receiving MDCc on the same day compared to urban patients. Same‐day multidisciplinary clinics may enhance timely cancer care delivery and increase adherence of provider recommendations, especially for underserved populations. 54 , 55 Given the travel and financial barriers associated with residing in rural areas, 53 our findings underscore the need for provider‐ and system‐focused interventions that leverage telehealth resources and promote same‐day MDCc in populations or areas with limited cancer resources.

We found that—after adjusting for patient, neighborhood, surgeon, and hospital characteristics—approximately 15% of the variation in receipt of MDCc was attributable to surgeons and hospitals. This highlights the important roles providers and health care organizations play in care delivery, which may be modifiable points for interventions to improve equitable delivery of quality cancer care and outcomes. For example, interprofessional skills trainings and policies that promote teamwork competencies, collaboration, and building referral networks across care delivery organizations may be avenues to increase MDCc. 56 Accreditation by the Commission on Cancer may also play another important role at both the surgeon and hospital level as it was associated with receipt of MDCc. Commission on Cancer accredits hospitals based on the standards that patients will receive cancer care using a multidisciplinary team approach. 57 Understanding how best to implement MDCc across diverse cancer care delivery settings with limited availability of specialty providers, variable knowledge about cancer treatments, and experiencing financial pressures (e.g., rural or DSH‐designated hospitals) are important next steps. 58 For example, although many rural hospitals and oncologists may not be able to provide onsite multidisciplinary services, there may be opportunities to draw on telehealth, virtual consultation, and visiting specialist models to facilitate guideline‐recommended cancer care. 53

Several limitations must be considered when interpreting these findings. First, surgery is standard of care for all three cancer types, and our analyses were limited to patients with surgical resection. However, we recognize that surgery is only one treatment modality, and future analyses should examine other health care organizational factors associated with receipt of guideline‐recommended radiation and systemic therapies. Next, we used a claims‐based algorithm to capture MDCc but acknowledge that claims‐based encounters with multiple providers do not necessarily equate to optimal care coordination. Nevertheless, prior reviews demonstrate that MDCc are associated with receipt of guideline‐concordant treatment, diagnostic accuracy, staging completeness, and timeliness. 3 Additionally, our 2‐month post‐diagnosis timeframe for capturing MDCc may underestimate specialist encounters after diagnosis and before surgical resection, 9 but we found no significant differences in receipt of MDCc within 2 months compared to 4 months or in the factors associated with MDCc at both time periods. We also were unable to capture discussion of clinical cases at multidisciplinary tumor boards or similar non‐billable conferences, which have been considered standard clinical practice in certain cancer care delivery settings (e.g., NCI‐designated Cancer Centers). Presentation at tumor boards, however, often remains reserved for particularly complex, unusual, or novel cases because of time and resource constraints.

Our neighborhood race and ethnicity measures were also limited to compositional measures (e.g., percentage of Black individuals). Future research should examine effects of comprehensive measures of systemic and structural inequities on receipt of MDCc and related outcomes, such as segregation based on housing patterns. 59 We also did not conduct geospatial analyses of factors, such as distance to tertiary care or specialty availability in a given geographical area, which may partially mediate disparities in the receipt of MDCc and contribute to disparities in access, receipt, and outcomes of cancer care among rural populations. 60 , 61 , 62 Finally, other factors not assessed in this study may influence receipt of MDCc, including patient and provider preferences, hospital organizational structures and processes, financial incentives, and referral policies. Despite these limitations, our findings can inform future research and interventions aiming to improve access to and receipt of MDCc among populations that experience health disparities.

5. CONCLUSION

The prevalence of MDCc is growing, albeit unequally for all cancer patients, with persistent racial, ethnic, and geographical disparities. Given that the surgeon‐ and hospital‐level factors explained 15% of the variation in MDCc, our findings can be used to inform future strategies that aim to synergistically address barriers at the patient, provider, health system, and neighborhood level to enhance equitable access to and receipt of multidisciplinary cancer care.

AUTHOR CONTRIBUTIONS

All authors (Janeth I. Sanchez, Michelle Doose, Chris Zeruto, Veronica Chollette, Natalie Gasca, Dana Verhoeven, and Sallie J. Weaver) contributed to the acquisition, analysis, and interpretation of the data, contributed to the critical revision for important intellectual content, and provided final approval of the version to be published. Janeth I. Sanchez, Michelle Doose, Veronica Chollette, and Sallie J. Weaver. contributed to the study concept and design, drafting the article, and statistical analyses. Chris Zeruto and Natalie Gasca contributed to the statistical analyses.

FUNDING INFORMATION

This article was prepared as part of the authors' official duties as employees of the US Federal Government. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the National Cancer Institute, National Institute on Minority Health and Health Disparities, or other federal agencies.

Supporting information

Appendix S1. Supplemental table.

ACKNOWLEDGMENTS

The authors would like to thank Drs. Shakuntala Malik, Anand Singla, Edward Sauter, Lindsey Enewold, and Michael Halpern for providing clinical and research expertise to this study.

Sanchez JI, Doose M, Zeruto C, et al. Multilevel factors associated with inequities in multidisciplinary cancer consultation. Health Serv Res. 2022;57(Suppl. 2):222‐234. doi: 10.1111/1475-6773.13996

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Associated Data

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Supplementary Materials

Appendix S1. Supplemental table.


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