UPDATE IN THE MANAGEMENT AND TREATMENT OF COLORECTAL CANCER. Edwin A. Empaynado, MD Advocare Colon and Rectal Surgical Specialists

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UPDATE IN THE MANAGEMENT AND TREATMENT OF COLORECTAL CANCER Edwin A. Empaynado, MD Advocare Colon and Rectal Surgical Specialists

WHAT IS COLON CANCER? WHAT CAUSES COLORECTAL CANCER? WHAT ARE THE RISK FACTORS SYMPTOMS DIAGNOSIS AND SCREENING STAGING OF COLON CANCER MEDICAL AND SURGICAL TREATMENT SURVIVORSHIP AND FOLLOW-UP PREVIEW OF PRESENTATION

Rank 1. 2. Common Types of Cancer Breast Cancer (Female) Lung and Bronchus Cancer Estimated New Cases 2018 Estimated Deaths 2018 266,120 40,920 234,030 154,050 3. Prostate Cancer 164,690 29,430 4. 5. Colorectal Cancer Melanoma of the Skin 140,250 50,630 91,270 9,320 6. Bladder Cancer 81,190 17,240 7. 8. Non-Hodgkin Lymphoma Kidney and Renal Pelvis Cancer 74,680 19,910 65,340 14,970 9. Uterine Cancer 63,230 11,350 10. Leukemia 60,300 24,370 HOW COMMON IS COLORECTAL CANCER? 3 rd most common cause of cancer in men and women of the U.S. or 8.1% of all new cancer cases in 2018 2 nd leading cause of cancer death among men and women of the U.S. or 8.3% of all cancer deaths in 2018 1 National Cancer Institute

WHAT AGE GROUP GETS COLORECTAL CANCER? Median age at diagnosis is 67 NCI, SEER 18 2011-2015

WHO DIES FROM COLORECTAL CANER? Median age at death 73

Rates of newly diagnosed cases of CRC have been decreasing 2.6% per year over past 10 years Rates of death from CRC cases have been decreasing 2.4% per year over past 10 years TRENDS IN NEW CASES OF COLORECTAL CANCER AND DEATH RATES NCI, SEER 9 1975-2015

TRENDS IN SURVIVAL RATES FOR COLORECTAL CANCER Percent surviving past 5 years from diagnosis of CRC 64.5 NCI, SEER 1975-2010

Population Health Data from 2013-2015 34.4/100,000 new cases diagnosed per year 14.5/100,000 number of deaths per year 4.5% lifetime risk of being diagnosed with colorectal cancer 1,332,085 people diagnosed with CRC in U.S. in 2015 PREVALENCE OF COLORECTAL CANCER 1 National Cancer Institute

WHAT IS COLON CANCER? Carcinoid tumors Gastrointestinal stromal tumors (GIST) Lymphomas Sarcomas Metestatic tumors (ie endometrial, ovarian, melanoma, etc.) Adenocarcinoma 96% of all colorectal cancers Cancer cells that arise from adenomatous polyps of mucous producing cells that normally help lubricate the inside lining of the colon and rectum

Cancers can be caused by changes in the DNA inside our cells called DNA mutations These mutations leads to uncontrolled cell growth and the development of cancerous tumors Inherited gene mutations occurs in about 10% cases Acquired gene mutations most common cause of CRC where a person acquires a mutation during a lifetime rather than inherited. WHAT CAUSES COLORECTAL CANCER?

A change in bowel habits Rectal bleeding or blood in your stool Abdominal discomfort and/or fullness that persists or recurs Feelings of incomplete evacuation Progressive weakness or fatigue Unexplained weight loss Anemia on recent bloodwork SYMPTOMS OF COLORECTAL CANCER

STOOL-BASED TESTS Highly sensitive fecal immunochemical test (FIT) every year Highly sensitive guaiac-based fecal occult blood test (gfobt) every year Multi-targeted stool DNA test (MT-sDNA) every 3 years VISUAL EXAMS OF THE COLON AND RECTUM Colonoscopy every 10 years CT colonoscopy (virtual colonoscopy) every 5 years Flexible sigmoidoscopy (FSIG) every 5 years SCREENING FOR COLORECTAL CANCER American Cancer Society (ACS) recommends average risk screening for CRC to start at age 45 through to age 75 at 10 year intervals Ages 76 through 85 screening is based on overall medical health and patient preferences People over 85 should no longer get colorectal screening 2 American Cancer Society

Average risk patients DO NOT have the following Personal history of colorectal cancer or colon polyps Family history of colorectal cancer Personal history of inflammatory bowel disease A confirmed hereditary colorectal cancer syndrome Personal history of abdominal and/or pelvic radiation to treat prior cancer WHAT IS AVERAGE RISK SCREENING?

Older age African-American race Personal history of colorectal cancer or polyps Inflammatory intestinal conditions Inherited syndromes Family history of colon cancer Low-fiber, high fat diet Sedentary lifestyle Diabetes Obesity Smoking Alcohol Radiation therapy for cancer Lynch Syndrome Familial Adenomatous Polyposis (FAP) WHAT ARE THE RISK FACTORS FOR COLORECTAL CANCER? Crohn s Disease Ulcerative Colitis

Patients at increased risk for colorectal cancer may need screening prior to age 45 and screened at more frequent intervals with colonoscopy Strong family history of colon cancer or polyps Personal history of colon cancer and/or polyps Personal history of inflammatory bowel disease Known family history of hereditary colorectal cancer syndrome Personal history of abdominal and/or pelvic radiation for treatment of prior cancer SCREENING FOR PEOPLE WHO ARE AT HIGHER RISK? Start screening prior to age 45 Consider more frequent screening, ie- every 3 to 5 years Screening at earlier age and every 1 to 2 years Start as early as teenage years with more frequent intervals Earlier age of screening and every 3 to 5 years

PROS Stool collection can done at home No prep required No need for sedation SCREENING MODALITIES Highly sensitive fecal immunochemical test (FIT) CONS Fails to detect some polyps and cancers Certain foods and medications may need to be avoided If positive, additional tests are needed to determine the source False-positive results Check stool samples for hidden (occult) blood. Test is done annually

PROS Does not require a bowel prep You can eat, drink and take your medications as usual before the test Stool collection done at home to avoid disruption of your daily routine CONS DNA stool test is less sensitive than colonoscopy at detecting precancerous polyps If abnormal, additional tests would be needed False-positive rates as high as 10-15% SCREENING MODALITIES Multi-targeted stool DNA test (MT-sDNA) Stool sample is used to look for DNA changes that would suggest the presence of colon cancer or precancerous conditions. Repeated every 3 years.

PROS Sedation is not required Less extensive bowel prep requirement Biopsies and/or other therapies can be performed through the scope SCREENING MODALITIES Flexible sigmoidoscopy (FSIG) CONS Upper colon abnormalities are not seen An enema prep is usually required You may need to change your diet and/or medication prior to test Rare complication of bowel injury and/or bleeding can occur Cramping and bloating after exam Tiny video camera that allows visualization of the rectum and lower part of the colon (sigmoid colon). Repeated every 5 years

PROS Test does not require sedation or insertion of a scope into the rectum CONS Requires a thorough bowel cleansing before the test May not detect small polyps or cancers Dietary and/or medication changes would be required Radiation exposure Purely diagnostic procedure; abormal findings would need colonoscopy follow-up Cramping and bloating SCREENING MODALITIES CT colonoscopy (virtual colonoscopy) CT scan produces initial cross-section images of abdominal organs that can be reconstructed in 3D images by a computer to detect abnormalities. Repeated every 5 years.

PROS The most sensitive test currently available for colon cancer screening. Visualize the entire colon Abnormal tissues can be biopsied and/or removed through the scope CONS Thorough bowel cleansing is required before the test Diet changes are required and medications may need to altered Sedation is usually required and would require someone to take you home Rare complication of bowel injury and/or bleeding from therapeutic sites Cramping and bloating after procedure SCREENING MODALITIES Colonoscopy Flexible tube with fiberoptic video camera is inserted into the rectum to detect abnormalities. Repeated every 10 years.

SHAPE o PEDUCULATED o SESSILE o SEMI-PEDUCULATED CELL PATTERN TUBULAR VILLOUS TUBULOVILLOUS HYPERPLASTIC SERRATED DYSPLASIA LOW-GRADE DYSPLASIA HIGH-GRADE DYSPLSIA ADENOMATOUS POLYPS Polyps are tissue growth from the inner lining of the colon that can be benign (non-cancerous) or grow into cancers (precancerous). Adenomatous feature is a description of a cell when viewed under a microscope that is different from normal cell appearance.

DIFFERENTIATION WELL DIFFERENTIATED MODERTELY DIFFERENTIATED POORLY DIFFERENTIATED INVASION VASCULAR LYMPHATIC LYMPHOVASCUALR HISTOLOGY MUCIN PRODUCING SIGNET-CELL INVASIVE ADENOCARCINOMA Adenocarinoma is a type of cancer from cells that form mucous producing glands lining the colonic wall. Invasive is a cell description suggesting spread beyond the inner lining of the colon.

Carcinoembryonic Antigen Test (CEA) CT scan 3T MRI TransRectal UltraSound (TRUS) PET/CT Scan o < 5ng/mL o Can be higher in smokers PRE-OP STAGING TESTS Radiographic staging of tumor Helps determine chemotherapy and/or radiation treatment plans Assess tumor resectability

85% of patients who present with colonic obstruction have CRC Only 40% of patients with obstructing left-sided colon cancer can be resected without the need of a colostomy Stent placement provides an effective solution to acute colonic obstruction Allows for bridge to elective and more favorable operative conditions Palliative treatment for advanced stage colon cancer TREATMENTS ENDOSCOPY AND COLONIC STENTING

Open Segmental colon resection Proximal diverting colostomy Laparoscopic colon resection Robotic colon resection Transanal full-thickness excision Transanal Endoscopic Microsurgery (TEM) TREATMENTS SURGERY PRIMARY CURATIVE TREATMENT

Segmental colon resection En bloc resection for negative radial margin Complete mesenteric lymph node resection High ligation of mesenteric pedicle Minimum 13 lymph nodes in specimen Total mesorectal excision Adequate tissue margin 5cm proximal and distal margins in colon cancer 1cm for sphincter-saving resection in rectal cancer TREATMENT ONCOLOGIC GOALS OF RESECTION

The weed Scan the lawn for other weeds Pull by the roots Normal turf around the weed Addition of fertilizer with weed killer

WHEN IS CHEMOTHERAPY GIVEN? Adjuvant chemo is given after surgery. The goal is to target small cancer cells throughout the body and help reduce recurrent cancer rates Neoadjuvant chemo is given before surgery, usually in combination with radiation, to reduce tumor size and improve resection Advanced cancers that has metastasized to other organs in efforts to improve quality of life HOW IS CHEMOTHERAPY GIVEN? Systemic chemotherapeutic drugs are either IV or orally given. Regional drugs are put right into an artery leading to a specific body part, ie liver, to reduce systemic side effects TREATMENTS CHEMOTHERAPY 5-Fluorouracil (5-FU) Capecitabine (Xeloda) Irinotecan (Camptosar) Oxaliplatin (Eloxatin) Trifluridine and Tipiracil (Lonsurf) 5-FU + Leucovorin FOLFOX FOLFIRI CAPIRI

Anti-angiogenesis therapy Bevacizumab (Avastin) Regorafenib (Stivarga) Ramucirumab (Cyramza) Epidermal growth factor receptor (EGFR) inhibitors Cetuximab (Erbitux) Panitumumab (Vectibix) Humanized antibody Pembrolizumab (Keytruda) TREATMENT TARGETED CHEMOTHERAPY Treatment on the cancer s specific molecular targets (ie -genes and proteins) Blocks tumor cell growth and spread Limits damage to healthy cells

Hair loss Mouth sores Loss of appetite Nausea and vomiting Diarrhea Immunosuppression Easy bruising or bleeding Fatigue Neuropathy SIDE EFFECTS OF CHEMOTHERAPY

Before surgery given with chemotherapy to improve efficacy (usually for rectal cancer) After surgery for cancer spread to other organs and/or peritoneal lining TREATMENTS RADIATION THERAPY High-energy x-rays used to destroy tumor cells and decrease local recurrence or spread of cancer During surgery, IORT to destroy tumor cells left behind after surgery Palliative radiation in advance cancers causing blockage, bleeding, or pain

External-beam radiation therapy (ERBT) Internal radiation therapy (brachytherapy) Stereotactic radiation therapy Endocavitary radiation therapy TREATMENT TYPES OF RADIATION THERAPY Shrink tumors before surgery to facilitate resection Alternative to surgery for patients who are not good surgical candidates Relieve symptoms of advance tumor growth such as pain and/or bleeding

STAGING COLORECTAL CANCER TNM Staging System T = Tumor N = Lymph Node M = Metastases(distant)

LOCAL TUMOR STAGING (T)

HOW DOES COLON CANCER METASTASIZE? Cancer cells spread by: Blood Lymphatics lymph nodes (N) Distant Organs lung, liver, peritoneal cavity (M) Medi Visuals, Inc., 2009

Stage 0 colorectal cancer Usual treatment with polypectomy alone with usually no additional surgery Stage I colorectal cancer Segmental surgical resection of tumor and mesenteric lymph nodes alone Stage II colorectal cancer Cure rates with segmental surgical resection alone are good and few benefit from additional adjuvant chemotherapy Stage III colorectal cancer Segmental surgical resection followed by adjuvant chemotherapy Stage IV (Metastatic) colorectal cancer Non-curative surgical resection aimed at palliating symptoms; palliative chemotherapy and/or radiation goals for longevity with quality of life TREATMENT OPTION BY STAGE Stages 0, I, II, and III are curable by surgery Stage II and III rectal cancer can receive radiation treatment before surgery

SURVIVAL RATES BASED ON STAGE 5-year survival rates for colorectal cancer based on initial stage of tumor

Regular physical examinations every 3-6 months CEA test Every 3-6 months CT scan annually for 3 years Sigmoidoscopy every 6 months Colonoscopy one year after surgery; then every 3-5 years depending on previous test result WHAT IS THE FOLLOW-UP CARE AFTER TREATMENT? 80% of recurrences are found within the first 2-3 years after surgery Primary goal of follow-up is early detection of recurrent cancer

UPDATE IN THE MANAGEMENT AND TREATMENT OF COLORECTAL CANCER Edwin A. Empaynado, MD, FACS Advocare Colon and Rectal Surgical Specialists