<?xml version="1.0"?>
<response><item key="0"><views_conditional_field>2024 Performance Period</views_conditional_field><field_cms_id>CMS646v4</field_cms_id><field_short_name></field_short_name><field_nqf>Not Applicable</field_nqf><field_quality_id>481</field_quality_id><body><![CDATA[<p>Percentage of patients initially diagnosed with non-muscle invasive bladder cancer and who received intravesical Bacillus-Calmette-Guerin (BCG) within 6 months of bladder cancer staging</p>
]]></body><field_definition><![CDATA[<div class="photoswipe-gallery"><p>Intravesical - Within the urinary bladder</p><p>Bacillus Calmette-Guerin (BCG) - A live attenuated strain of Mycobacterium bovis, first indicated as a tuberculosis vaccine, has had widespread use in intravesical immunotherapy since the 1970's.</p><p>Tumor location: urinary bladder</p><p>Histology: urothelial carcinoma</p><p>Primary Tumor (T) stage:</p><p>Ta - Noninvasive and high <a href="/glossary/grading-recommendations-assessment-development-and-evaluation-grade" title="Grading of Recommendations Assessment, Development, and Evaluation (GRADE) is a transparent framework for developing and presenting summaries of evidence and provides a systematic approach for making clinical practice recommendations. It is the most widely adopted tool for grading the quality of evidence and for making recommendations. " class="glossify-tooltip-link">grade</a></p><p>Tis - Carcinoma in situ: "flat tumor"</p><p>T1- tumor invades subepithelial connective tissue (high grade or low grade)</p></div>]]></field_definition><field_initial_patient_population><![CDATA[<div class="photoswipe-gallery"><p>All patients initially diagnosed with T1, Tis or high <a href="/glossary/grading-recommendations-assessment-development-and-evaluation-grade" title="Grading of Recommendations Assessment, Development, and Evaluation (GRADE) is a transparent framework for developing and presenting summaries of evidence and provides a systematic approach for making clinical practice recommendations. It is the most widely adopted tool for grading the quality of evidence and for making recommendations. " class="glossify-tooltip-link">grade</a> Ta non-muscle invasive bladder cancer with bladder cancer staging within 6 months before to 6 months after the start of the measurement period and a qualified encounter in the measurement period</p></div>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<div class="photoswipe-gallery"><p>Intravesical Bacillus-Calmette Guerin (BCG) instillation for initial dose or series:</p><p>BCG is initiated within 6 months of the bladder cancer staging</p></div>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<div class="photoswipe-gallery"><p>Not Applicable</p></div>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<div class="photoswipe-gallery"><p>Equals Initial Population</p></div>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<div class="photoswipe-gallery"><p>Immunosuppressed patients, includes HIV and immunocompromised state, with a diagnosis prior to Bladder Cancer Staging</p><p>Immunosuppressive drug therapy starting on or before Bladder Cancer Staging</p><p>Active Tuberculosis diagnosis during the Bladder Cancer Staging</p><p>Mixed histology urothelial cell carcinoma including micropapillary, plasmacytoid, sarcomatoid, adenocarcinoma and squamous disease prior to Bladder Cancer Staging</p><p>Patients who undergo cystectomy, chemotherapy or radiation within 6 months of Bladder Cancer Staging</p></div>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<div class="photoswipe-gallery"><p>Unavailability of BCG within 6 months after Bladder Cancer Staging</p></div>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/oregon-urology" hreflang="en">Oregon Urology</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<div class="photoswipe-gallery"><p>A higher score is the preferred result and indicates better quality</p></div>]]></field_improvement_notation><field_guidance>Ta bladder cancer must be high grade Ta only and is supported by the 2016 AUA guidelines and 2018 NCCN guidelines.The BCG dose can be full or partial and can be from any lot or manufacturer.This eCQM is a patient-based measure.Telehealth encounters are not eligible for this measure because the measure requires a clinical action that cannot be conducted via telehealth.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.</field_guidance><field_telehealth_eligible>No</field_telehealth_eligible><field_rationale><![CDATA[<div class="photoswipe-gallery"><p>Bladder cancer is ranked 10th for new cancer cases in 2020 and is the 9th leading cause of cancer death in the United States. There are 81,400 estimated new cases in 2020 and 17,980 estimated deaths in 2020. In 2016, there were an estimated 699,450 people living with bladder cancer in the United States. Early detection (discovery of cancer in situ or localized to the primary site) is found in 85% of the patients, and with these there is a five-year survival rate of 95.8% for In Situ and 69.2% for Localized. Bladder cancer is rarely found in patients under age 20, with the median age of diagnosis being 73 (NIH, 2020).</p><p>National Comprehensive Cancer Network (NCCN) Guidelines for Bladder Cancer (version 6.2020) defines intravesical BCG as Category 1 Treatment for Ta - high <a href="/glossary/grading-recommendations-assessment-development-and-evaluation-grade" title="Grading of Recommendations Assessment, Development, and Evaluation (GRADE) is a transparent framework for developing and presenting summaries of evidence and provides a systematic approach for making clinical practice recommendations. It is the most widely adopted tool for grading the quality of evidence and for making recommendations. " class="glossify-tooltip-link">grade</a>, T1 and Tis non-muscle invasive bladder cancer. Most public data reflects prophylactic or adjuvant use of intravesical therapy with the goal of preventing recurrence or delaying progression to a higher grade or stage. BCG has been shown to be effective as prophylaxis to prevent bladder cancer recurrences following TURBT. The NCCN Bladder Cancer Panel Members recommend BCG as the preferred option over Mitomycin C for adjuvant treatment of high-grade lesions (Ta). BCG is also standard therapy for Primary Tis. Most T1 lesions are high risk and are similarly treated with adjuvant intravesical therapy with BCG being a Category 1 recommendation. (NCCN, 2020).</p></div>]]></field_rationale><field_stratification><![CDATA[<div class="photoswipe-gallery"><p>None</p></div>]]></field_stratification><field_riskadjustment><![CDATA[<div class="photoswipe-gallery"><p>None</p></div>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<div class="photoswipe-gallery"><p>Intravesical BCG should be administered within 6 months of the initial diagnosis of non-muscle invasive bladder cancer. It may be administered 3-4 weeks after resection, but there needs to be pathological tumor confirmation and must be withheld if there is traumatic catheterization, bacteriuria, persistent gross hematuria, persistent severe local symptoms or systemic symptoms. The normal induction course is 6 weekly instillations of intravesical BCG (AUA Non-Muscle Invasive Bladder Cancer and American Urological Association (AUA) Guideline for the Management of Non-muscle Invasive Bladder Cancer: Stages Ta High Risk, T1 and TIS).</p></div>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item><item key="1"><views_conditional_field>2025 Performance Period</views_conditional_field><field_cms_id>CMS646v5</field_cms_id><field_short_name></field_short_name><field_nqf>Not Applicable</field_nqf><field_quality_id>481</field_quality_id><body><![CDATA[<p>Percentage of patients initially diagnosed with non-muscle invasive bladder cancer and who received intravesical Bacillus-Calmette-Guerin (BCG) within 6 months of bladder cancer staging</p>]]></body><field_definition><![CDATA[<p>Intravesical - Within the urinary bladder</p><p>Bacillus Calmette-Guerin (BCG) - A live attenuated strain of Mycobacterium bovis, first indicated as a tuberculosis vaccine, has had widespread use in intravesical immunotherapy since the 1970's.</p><p>Tumor location: urinary bladder</p><p>Histology: urothelial carcinoma</p><p>Primary Tumor (T) stage:</p><p>Ta - Noninvasive and high grade</p><p>Tis - Carcinoma in situ: "flat tumor"</p><p>T1- tumor invades subepithelial connective tissue (high grade or low grade)</p>]]></field_definition><field_initial_patient_population><![CDATA[<p>All patients initially diagnosed with T1, Tis or high grade Ta non-muscle invasive bladder cancer with bladder cancer staging within 6 months before to 6 months after the start of the measurement period and a qualified encounter in the measurement period</p>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<p>Intravesical Bacillus-Calmette Guerin (BCG) instillation for initial dose or series:</p><p>BCG is initiated within 6 months of the bladder cancer staging</p>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<p>Not Applicable</p>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<p>Equals Initial Population</p>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<p>Immunosuppressed patients, includes HIV and immunocompromised state, with a diagnosis prior to Bladder Cancer Staging.</p><p>Immunosuppressive drug therapy starting on or before Bladder Cancer Staging.</p><p>Active Tuberculosis diagnosis during the Bladder Cancer Staging.</p><p>Mixed histology urothelial cell carcinoma including micropapillary, plasmacytoid, sarcomatoid, adenocarcinoma and squamous disease prior to Bladder Cancer Staging.</p><p>Patients who undergo cystectomy, chemotherapy or radiation within 6 months prior to Bladder Cancer Staging.</p>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<p>Unavailability of BCG within 6 months after Bladder Cancer Staging</p>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/oregon-urology" hreflang="en">Oregon Urology</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<p>A higher score is the preferred result and indicates better quality</p>]]></field_improvement_notation><field_guidance>Ta bladder cancer must be high grade Ta only and is supported by the 2016 AUA guidelines and 2018 NCCN guidelines.The BCG dose can be full or partial and can be from any lot or manufacturer.This eCQM is a patient-based measure.Telehealth encounters are not eligible for this measure because the measure requires a clinical action that cannot be conducted via telehealth.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.</field_guidance><field_telehealth_eligible>No</field_telehealth_eligible><field_rationale><![CDATA[<p>Bladder cancer is ranked 10th for new cancer cases in 2020 and is the 9th leading cause of cancer death in the United States. There are 81,400 estimated new cases in 2020 and 17,980 estimated deaths in 2020. In 2016, there were an estimated 699,450 people living with bladder cancer in the United States. Early detection (discovery of cancer in situ or localized to the primary site) is found in 85% of the patients, and with these there is a five-year survival rate of 95.8% for In Situ and 69.2% for Localized. Bladder cancer is rarely found in patients under age 20, with the median age of diagnosis being 73 (NIH, 2020).</p><p>National Comprehensive Cancer Network (NCCN) Guidelines for Bladder Cancer (version 6.2021) defines intravesical BCG as Category 1 Treatment for Ta - high grade, T1 and Tis non-muscle invasive bladder cancer. Most public data reflects prophylactic or adjuvant use of intravesical therapy with the goal of preventing recurrence or delaying progression to a higher grade or stage. BCG has been shown to be effective as prophylaxis to prevent bladder cancer recurrences following TURBT. The NCCN Bladder Cancer Panel Members recommend BCG as the preferred option over Mitomycin C for adjuvant treatment of high-grade lesions (Ta). BCG is also standard therapy for Primary Tis. Most T1 lesions are high risk and are similarly treated with adjuvant intravesical therapy with BCG being a Category 1 recommendation. (NCCN, 2021).</p>]]></field_rationale><field_stratification><![CDATA[<p>None</p>]]></field_stratification><field_riskadjustment><![CDATA[<p>None</p>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<p>Intravesical BCG should be administered within 6 months of the initial diagnosis of non-muscle invasive bladder cancer. It may be administered 3-4 weeks after resection, but there needs to be pathological tumor confirmation and must be withheld if there is traumatic catheterization, bacteriuria, persistent gross hematuria, persistent severe local symptoms or systemic symptoms. The normal induction course is 6 weekly instillations of intravesical BCG (AUA Non-Muscle Invasive Bladder Cancer and American Urological Association (AUA) Guideline for the Management of Non-muscle Invasive Bladder Cancer: Stages Ta High Risk, T1 and TIS).</p>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item><item key="2"><views_conditional_field>2026 Performance Period</views_conditional_field><field_cms_id>CMS646v6</field_cms_id><field_short_name></field_short_name><field_nqf>Not Applicable</field_nqf><field_quality_id>481</field_quality_id><body><![CDATA[<p>Percentage of patients initially diagnosed with non-muscle invasive bladder cancer and who received intravesical Bacillus-Calmette-Guerin (BCG) within 6 months of bladder cancer staging</p>]]></body><field_definition><![CDATA[<p>Intravesical - Within the urinary bladder</p><p>Bacillus Calmette-Guerin (BCG) - A live attenuated strain of Mycobacterium bovis, first indicated as a tuberculosis vaccine, has had widespread use in intravesical immunotherapy since the 1970's.</p><p>Tumor location: urinary bladder</p><p>Histology: urothelial carcinoma</p><p>Primary Tumor (T) stage:</p><p>T1- tumor invades subepithelial connective tissue (high grade or low grade)</p><p>Tis - Carcinoma in situ: "flat tumor"</p><p>Ta - Noninvasive and high grade</p>]]></field_definition><field_initial_patient_population><![CDATA[<p>All patients initially diagnosed with T1, Tis or high grade Ta non-muscle invasive bladder cancer with bladder cancer staging within 6 months before to 6 months after the start of the measurement period and a qualified encounter in the measurement period</p>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<p>Intravesical Bacillus-Calmette Guerin (BCG) instillation for initial dose or series: BCG is initiated within 6 months of the bladder cancer staging</p>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<p>None</p>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<p>Equals Initial Population</p>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<p>Immunosuppressed patients, includes HIV and immunocompromised state, with a diagnosis prior to Bladder Cancer Staging.</p><p>Immunosuppressive drug therapy starting on or before Bladder Cancer Staging.</p><p>Active Tuberculosis diagnosis during the Bladder Cancer Staging.</p><p>Mixed histology urothelial cell carcinoma including micropapillary, plasmacytoid, sarcomatoid, adenocarcinoma and squamous disease prior to Bladder Cancer Staging.</p><p>Patients who undergo cystectomy, chemotherapy or radiation within 6 months prior to Bladder Cancer Staging.</p>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<p>Unavailability of BCG within 6 months after Bladder Cancer Staging</p>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/oregon-urology" hreflang="en">Oregon Urology</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<p>Higher score indicates better quality</p>]]></field_improvement_notation><field_guidance>Ta bladder cancer must be high grade Ta only and is supported by the 2016 AUA guidelines and 2018 NCCN guidelines.The BCG dose can be full or partial and can be from any lot or manufacturer. This eCQM is a patient-based measure.Telehealth encounters are not eligible for this measure because the measure requires a clinical action that cannot be conducted via telehealth.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.</field_guidance><field_telehealth_eligible>No</field_telehealth_eligible><field_rationale><![CDATA[<p>Bladder cancer is ranked 10th for new cancer cases in 2020 and is the ninth leading cause of cancer death in the United States. There are 81,400 estimated new cases in 2020 and 17,980 estimated deaths in 2020. In 2016, an estimated 699,450 people were living with bladder cancer in the United States. Early detection (discovery of cancer in situ or localized to the primary site) is found in 85% of the patients, and with these there is a five-year survival rate of 95.8% for In Situ and 69.2% for Localized. Bladder cancer is rarely found in patients under age 20, with the median age of diagnosis being 73 (NIH, 2020).</p><p>National Comprehensive Cancer Network (NCCN) Guidelines for Bladder Cancer (version 6.2021) defines intravesical BCG as Category 1 Treatment for T1, Tis and Ta - high grade, non-muscle invasive bladder cancer. Most public data reflects prophylactic or adjuvant use of intravesical therapy to prevent recurrence or delay progression to a higher grade or stage. BCG has been shown to be effective as prophylaxis to prevent bladder cancer recurrences following TURBT. The NCCN Bladder Cancer Panel Members recommend BCG as the preferred option over Mitomycin C for adjuvant treatment of high-grade lesions (Ta). BCG is also standard therapy for Primary Tis. Most T1 lesions are high-risk and are similarly treated with adjuvant intravesical therapy, with BCG being a Category 1 recommendation. (NCCN, 2021).</p>]]></field_rationale><field_stratification><![CDATA[<p>None</p>]]></field_stratification><field_riskadjustment><![CDATA[<p>None</p>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<p>Intravesical BCG should be administered within 6 months of the initial diagnosis of non-muscle invasive bladder cancer. It may be administered 3-4 weeks after resection, but there needs to be pathological tumor confirmation and must be withheld if there is traumatic catheterization, bacteriuria, persistent gross hematuria, persistent severe local symptoms or systemic symptoms. The normal induction course is 6 weekly instillations of intravesical BCG (AUA Non-Muscle Invasive Bladder Cancer and American Urological Association (AUA) Guideline for the Management of Non-muscle Invasive Bladder Cancer: Stages T1, TIS, and Ta High Risk.</p>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item></response>
