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Cancer Management Handbook
 

Home » Cancer Management Handbook » Chapter 24

Cancer Management: A Multidisciplinary Approach, 12th Edition (2009).
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Chapter 24 
By Ronald T. Mitsuyasu, MD, and Jay S. Cooper, MD | March 12, 2010

Treatment

Treatment of preinvasive disease
Cryotherapy, laser therapy, cone biopsy, and loop electrosurgical excision procedure have all been used to treat preinvasive disease in HIV-infected patients. Short-term recurrence rates of 40% to 60% have been reported.

Determinants of recurrence
Immune status of the patient seems to be the most important determining factor for recurrence. Close surveillance after initial therapy is critical, and repetitive treatment may be necessary to prevent progression to more invasive disease.

Treatment of cervical carcinoma
The same principles that guide oncologic management of the immunocompetent patient with cervical carcinoma (see chapter 17) are utilized in AIDS patients with this cancer.

Resection
Resection can be undertaken for the usual indications, and surgical decisions should be based on oncologic appropriateness and not on HIV status.

Radiation therapy
As most AIDS patients with cervical cancer present with advanced disease, radiation therapy is indicated more often than surgery. If the patient’s overall physical condition permits, treatment regimens are identical to those used for the same stage disease in uninfected individuals (see chapter 17). It is important to note that the standard of care for advanced carcinoma of the cervix (stages III–IV, without hematogeneous dissemination) now includes a combination of irradiation and concurrent cisplatin-based chemotherapy. At present, there is insufficient evidence to suggest that irradiation or other treatments for cervical carcinoma in AIDS patients is any less effective than in similar non–HIV-infected individuals.

Chemotherapy
Antineoplastic regimens, such as cisplatin (50 mg/m2) or carboplatin (200 mg/m2), bleomycin (20 U/m2; maximum, 30 U), and vincristine (1 mg/m2), have been used in patients with metastatic or recurrent disease. Vigorous management of side effects and complications of these treatments and of AIDS itself must be provided.

ANAL CARCINOMA

Although anal carcinoma is not currently an AIDS-defining illness, the incidence of this tumor is increasing in the population at risk for HIV infection. The incidence of anal carcinoma in homosexual men in a San Francisco study was estimated at between 25 and 87 cases per 100,000, compared with 0.7 case per 100,000 in the entire male population.

Etiology and risk factors

HPV
Precursor lesions of anal intraepithelial neoplasia (AIN), also known as anal SILs, have been found to be associated with HPV infection, typically with oncogenic serotypes, eg, types 16 and 18. Cytologic abnormalities occur in nearly 40% of patients, especially those with CD4 cell counts < 200 cells/μL. Abnormal cytology may predict the later development of invasive carcinoma.

Signs and symptoms

Rectal pain, bleeding, discharge, and symptoms of obstruction or a mass lesion are the most frequent presenting symptoms.

Screening and diagnosis

Studies to evaluate the usefulness of anoscopy with frequent anal cytology have been undertaken to determine whether early detection of AIN may result in interventions that would prevent the development of invasive tumors.

Work-up of patients with anal carcinoma
For patients with anal carcinoma, determination of the extent of local disease, as well as full staging for dissemination, should be undertaken (see chapter 13).

Pathology

Squamous cell carcinoma
The majority of anal carcinomas are of the squamous cell type.

Histologic grading
The grading for AIN is similar to that for CIN, with AIN-1 denoting low-grade dysplasia and AIN-2 and AIN-3 referring to higher grade dysplastic lesions. The gross appearance of lesions on anoscopy does not predict histologic grade. Higher grade dysplastic lesions are seen in patients with lower CD4 cell counts.

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Table of Contents

Chapter 1: Head and Neck Tumors

Chapter 2: Thyroid and Parathyroid Cancers

Chapter 3: Non-Small-Cell Lung Cancer

Chapter 4: Small-Cell Lung Cancer, Mesothelioma, and Thymoma

Chapter 5: Breast Cancer Overview

Chapter 6: Stages 0 and I breast cancer

Chapter 7: Stage II breast cancer

Chapter 8: Stages III and IV breast cancer

Chapter 9: Esophageal cancer

Chapter 10: Gastric cancer

Chapter 11: Pancreatic, neuroendocrine GI, and adrenal cancers

Chapter 12: Liver, gallbladder, and biliary tract cancers

Chapter 13: Colon, rectal, and anal cancers

Chapter 14: Prostate cancer

Chapter 15: Testicular cancer

Chapter 16: Urothelial and kidney cancers

Chapter 17: Cervical cancer

Chapter 18: Uterine corpus tumors

Chapter 19: Ovarian cancer

Chapter 20: Melanoma and other skin cancers

Chapter 21: Bone sarcomas

Chapter 22: Soft-tissue sarcomas

Chapter 23: Primary and metastatic brain tumors

Chapter 24: AIDS-related malignancies

Chapter 25: Carcinoma of an unknown primary site

Chapter 26: Hodgkin lymphoma

Chapter 27: Non-Hodgkin lymphoma

Chapter 28: Multiple myeloma and other plasma cell dyscrasias

Chapter 29: Acute leukemias

Chapter 30: Chronic myeloid leukemia

Chapter 31: Chronic lymphocytic leukemia

Chapter 32: Myelodysplastic syndromes

Chapter 33: Hematopoietic cell transplantation

Chapter 34: Pain management

Chapter 35: Management of nausea and vomiting

Chapter 36: Depression, anxiety, and delirium

Chapter 37: Fatigue and dyspnea

Chapter 38: Anorexia and cachexia

Chapter 39: Oncologic emergencies and paraneoplastic syndromes

Chapter 40: Infectious complications

Chapter 41: Fluid complications

Color atlas The ABCDEs of moles and melanomas

Color atlas 2: Skin lesions

Color atlas 3: Dermatologic toxicities associated with targeted therapies

Appendix 1: Response Evaluation Criteria and Performance Scales

Appendix 2: Cancer Information on the Internet

Appendix 3: Cancer Drugs and Indications Newly Approved by the US Food and Drug Administration

Appendix 4: Chemotherapeutic Agents Their Uses, Dosages, and Toxicites

 
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