Arimidex

A cancer survivor is "anyone who has been diagnosed with cancer from the time of diagnosis through the balance of his or her life." (1) Continued advances in cancer treatment have led to marked improvements in cure rates, resulting in almost 10 million U.S. cancer survivors. (2) Nearly two thirds of all cancer patients survive for at least five years, and survival rates are much higher for many common types of cancer (Table 1). (2,3) Cancer survivors are at increased risk for recurrence of the original cancer and development of second primary malignancies as a result of cancer therapy and other risk factors. Prolonged monitoring and treatment are warranted for long-term side effects of surgical, radiation, or cytotoxic therapy.

Approximately 70 percent of cancer patients have comorbid conditions, (4) requiring a comprehensive approach to medical care. Family physicians often have established long-term relationships with these patients and their families, and most cancer patients continue to receive medical care from their family physicians. In addition to overseeing care, acting as a patient advocate, and providing support for family members, the family physician can ensure continued surveillance, provision of preventive care, and management of medical problems.

This article provides an overview of ongoing care and follow-up for cancer survivors. It summarizes surveillance recommendations for the detection of recurrent cancer and second primaries, describes monitoring for potential physical and psychosocial complications of treatment, and addresses other considerations such as genetic risk assessment among survivors of breast, colorectal, and prostate cancers, childhood acute lymphoblastic leukemia, and Hodgkin's disease. These cancers were selected as examples based on their high prevalence or high rates of survival. Tables 2 (5,6) and 3 summarize surveillance information.

[TABLE 2 OMITTED]

Breast Cancer Survivors

More than 2.1 million U.S. women are breast cancer survivors. (2) Current recommendations for surveillance after primary breast cancer include monthly self-examination of the breasts, annual mammography of preserved breast tissue, and a careful history and physical examination every six months for five years, and annually thereafter. (7) Intensive surveillance using laboratory and imaging tests does not improve overall survival or quality of life. (8) Routine surveillance using bone scans, chest radiographs, and blood tests for tumor markers is not recommended. (8)

Breast cancer survivors have an increased risk of second primary cancers involving the ipsilateral and contralateral breast, ovaries, colon, and rectum. (9) Most recurrent breast cancers arise within the first five years following treatment. Recurrence rates are very low in patients with primary tumors smaller than 1 cm and negative axillary nodes. (10) Non-specific symptoms (e.g., weight loss, persistent cough) or physical findings (e.g., breast or chest wall changes, adenopathy) are common indicators of breast cancer recurrence (11) that should be evaluated thoroughly and specifically sought during regular surveillance.

Breast cancer survivors also may develop physical complications of treatment such as lymphedema, premature menopause, neurocognitive changes, and osteopenia or osteoporosis, as well as psychologic distress related to coping and sexuality changes. (9) Up to 30 percent of breast cancer patients treated with chemotherapy experience cognitive effects, sometimes referred to as "chemo brain." (12) These complications warrant discussion and possible intervention with cognitive-behavior therapy or pharmacotherapy. Studies of various treatment strategies are underway. (12) Lymphedema occurs in 20 to 30 percent of breast cancer patients treated surgically (13) and often responds to early conservative management by physical therapists specializing in this condition. (14) Meticulous skin care is recommended to reduce the risk of local and systemic infection arising from impaired lymphatic return. (Additional information is available online at http://www.cancer.org or through the National Lymphedema Network at 800-541-3259.)

Although tamoxifen (Nolvadex) has been demonstrated to reduce the risk of recurrent breast cancers (15) and maintain bone density, (16) it does increase the risk of uterine cancer. Annual monitoring by pelvic examination is indicated. (7) Recent data suggest that the use of aromatase inhibitors (anastrozole [Arimidex]) in post-menopausal, estrogen receptor-positive breast cancer patients may have greater efficacy and fewer side effects than tamoxifen in the adjuvant setting. (17)

Finally, a review of family history may suggest a hereditary component in breast cancer. Approximately 5 to 10 percent of breast cancers are caused by mutations in cancer-susceptibility genes, most commonly BRCA1 and BRCA2. (18) The role of genetics professionals is important in assessing individual genetic risk and the need for specific testing among these patients and their family members. (A directory of professionals can be found online at http://cancer.gov/search/genetics_services/).

Colorectal Cancer Survivors

For the more than 1 million colorectal cancer survivors in the United States, (2) the prompt detection of recurrent disease can result in improved survival and potential cure. The risk of recurrence is highest in the first five years following resection; thus, frequent follow-up and surveillance have been recommended during this time (Table 2). (5,6) Although a recent meta-analysis (5,19) has shown a survival benefit of 19 percent at five years in patients undergoing intensive follow-up, the American Society of Clinical Oncology (20) and the National Comprehensive Care Network (NCCN) (7) guidelines have limited their follow-up recommendations to history taking, physical examination, carcinoembryonic antigen testing, and colonoscopy. Interpretation of the meta-analysis is complicated by the variety of tests and follow-up schedules used in the studies reviewed. While in this meta-analysis more intensive follow-up was associated with an overall survival benefit, it is not possible to infer an optimal combination of tests or frequency of clinical follow-up for intensive colorectal cancer surveillance. (5)

History taking, physical examinations, and carcinoembryonic antigen monitoring are recommended every three months for the first two years following treatment, and then every six months for the next three years (7,20) (Table 2). (5,6) Patients with carcinoembryonic antigen elevations should be investigated with computed tomography (CT), positron-emission tomography, or colonoscopy, as appropriate, to identify the site of recurrence and its potential for resection. Elevated carcinoembryonic antigen levels may precede symptoms by as much as three to eight months. (21) Surveillance colonoscopy is recommended 12 months postoperatively, provided a full colonoscopy was performed before surgery (at six months if otherwise), and then every three to five years if no abnormalities are detected. (7) Use of routine chest radiographs for annual follow-up is not recommended. (7)

Many survivors of colorectal cancer need to adapt to treatment-associated effects such as fecal incontinence and adhesions. Radiation therapy can cause persistent diarrhea and episodic bleeding resulting from radiation proctitis. This may be treated symptomatically (22) with antimotility agents such as loperamide (Imodium). In severe radiation proctitis, a short course of hydrocortisone foam enemas may be beneficial. Family physicians should be alert to the challenges of ostomy care, including issues of body image and sexuality. (23) Consultation with an ostomy specialist can help family physicians develop individualized treatment recommendations and supportive care.

Colorectal cancer can be organized into three categories based on family history: (1) sporadic (about 60 percent of all cases)--no family history; (2) familial (about 30 percent of cases)--several affected family members; and (3) hereditary (about 10 percent of cases)--mainly genetic syndromes such as familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC). (20) FAP has a classic presentation with the formation of hundreds to thousands of adenomatous polyps within the colon and rectum at an early age. Persons with FAP have a nearly 100 percent chance of developing cancer by age 50.24 Persons with HNPCC have an increased risk for colorectal cancers, as well as cancers of the endometrium, small bowel, ureter, and renal pelvis. (25) Women with HNPCC have a lifetime risk of 30 to 60 percent of developing endometrial cancer. (26) Genetic counseling can help determine familial risk and the need for regular testing. Nonsteroidal anti-inflammatory drugs such as aspirin and sulindac (Clinoril) have been shown to have a protective effect against colorectal cancers and polyps. (27,28)

Prostate Cancer Survivors

Approximately 98 percent of prostate cancer patients are alive five years after diagnosis, with many men thriving for extended periods (Table 1). (2,3) As a result, the number of prostate cancer survivors is estimated to exceed 1.7 million persons. (2)

Surveillance for prostate cancer survivors includes annual digital rectal examination and monitoring of prostate-specific antigen (PSA) levels every six months for five years, and then annually. (7) The serum PSA declines to undetectable levels following radical prostatectomy; a slower decline is noted after radiation therapy. (29) Elevated serum PSA levels following the initial decline attained with definitive therapy indicates disease recurrence. More recently, the concept of PSA velocity, or the change in PSA level over time, is gaining attention. Preoperative PSA velocity during the year before diagnosis has been associated with the risk of death from prostate cancer. (30) Postoperative PSA velocity, along with Gleason score and cancer staging, has been shown to predict disease recurrence. (29)

Although recurrence represents the most serious threat to patients' health, complications resulting from therapy are of greater concern to patients and significantly affect quality of life. A study (31) of patients with localized prostate cancer who were assigned randomly to surgery or watchful waiting noted more erectile dysfunction and urinary leakage in those treated surgically. Phosphodiesterase type 5 inhibitors (tadalafil [Cialis], vardenafil [Levitra], sildenafil [Viagra]) can be used to treat erectile dysfunction in patients who have completed nerve-sparing prostatectomy. (32) These inhibitors can potentiate the hypotensive effects of nitrates and alpha blockers.

Published data on treatment complications in prostate cancer vary depending on the type of therapy, outcome definitions, and study participants. An increased incidence of bladder cancer has been noted among prostate cancer patients treated with radiation therapy, but this could be attributable to increased surveillance. (33)

Many cases of prostate cancer have a familial component. The risk to an individual increases as the number of affected family members increases. (34) In addition, men with family members affected by breast or ovarian cancers may be at increased risk for prostate cancer caused by BRCA1 and BRCA2 mutations. (35) Consultation with a genetics professional for risk assessment and possible testing may be useful.

Childhood Cancer Survivors

Providing risk-based health care for the growing number of survivors of childhood and adolescent cancer (currently 270,000 in the United States) is challenging, given the risk for a variety of late complications associated with therapy. Chemotherapy and radiation therapy administered during years of growth and development significantly influence the aging of various organ systems. Nearly one half of young adult survivors of childhood cancer have at least one major adverse outcome. (35) Later cancer-related effects predominantly increase the risk for early mortality caused by second cancers and cardiac or pulmonary disease. (36) Single-institution studies (37) estimate that two thirds of survivors have at least one chronic or late-occurring complication of cancer therapy, with about one third having serious or life-threatening complications. The incidence of most late effects increases with age, with some effects not becoming apparent clinically until decades after therapy.

With many of these late effects, there is a window of opportunity for surveillance and early diagnosis. Currently, testing for the early detection of cancer in childhood cancer survivors lags below desired levels, despite the increased risk. (38) Periodic evaluation is recommended and should include a systematic plan for surveillance and prevention, incorporating risks based on the previous cancer or cancer therapy, genetic predispositions, personal behaviors, and comorbid health conditions. (39)

Assessing and stratifying risks for a heterogeneous population of childhood cancer survivors treated in different eras is difficult. The Children's Oncology Group recently developed a set of guidelines for the long-term follow-up care of survivors of childhood, adolescent, and young adult cancers (http://www.survivorshipguidelines.org). However, the relatively limited size of these populations precludes studies assessing the extent to which surveillance impacts measurable reductions in morbidity or mortality. Two case studies are presented that briefly illustrate risks for late effects faced by survivors.

Illustrative Cases

CASE ONE

A 27-year-old man had been diagnosed in 1980, when he was two years old, with acute lymphoblastic leukemia, the most common childhood cancer. He was treated with 24 Gray (Gy) cranial radiotherapy, methotrexate (Trexall), 6-mercaptopurine (Purinethol), vincristine (Oncovin), prednisone, and asparaginase (Elspar). He has not received any specific follow-up for more than 10 years.

Treatment that occurred during the early 1980s is associated with cognitive dysfunction, growth hormone deficiency, obesity, osteoporosis, and psychosocial problems. (40) In addition to a history and physical examination (including calculation of body mass index), surveillance recommendations include checking thyroid-stimulating hormone and free-thyroxine levels for central hypothyroidism. (40) An assessment for osteoporosis should be considered because treatment with methotrexate and prednisone is associated with early onset of this condition. (40) If the patient is obese, blood pressure, dyslipidemia, and insulin resistance also should be assessed. (40)

Periodontal disease is associated with cranial radiotherapy; therefore, dental cleaning every six months and an annual evaluation by a dentist are recommended. (40) Assessment of educational and vocational progress is important, and neurocognitive testing should be considered if problems are apparent. Patients who received more than 24 Gy of cranial radiotherapy appear to be at increased risk of cognitive dysfunction. All survivors of childhood cancers are at increased risk for depression and should be screened and treated appropriately. (40)

CASE TWO

A 28-year-old woman who had been diagnosed with Hodgkin's disease at age 15 presents with a breast mass. Previously, she had been treated with staging laparotomy and splenectomy followed by radiation therapy (45 Gy to the mediastinum; 36 Gy to periaortic and perisplenic lymph nodes; 21 Gy to the pelvis) and chemotherapy using nitrogen mustard (mechlorethamine [Mustargen]), procarbazine (Matulane), 125 mg per [m.sup.2] of doxorubicin (Adriamycin), bleomycin (Blenoxane), vincristine, vinblastine (Velban), and prednisone.

Female Hodgkin's disease survivors treated with mediastinal, mantle, or chest radiation face a significant increase in the risk for breast cancer, which can occur as quickly as six to eight years after radiation therapy. The 30-year cumulative incidence is about 17 percent. (41) Because of a cumulative risk of 35 percent for breast cancer at 40 years, surveillance with clinical breast examinations, beginning at 20 years of age, and mammography, beginning at 25 years of age, has been recommended for female Hodgkin's disease survivors who were treated with chest irradiation. (42) These patients also are at increased risk for second primary cancers (e.g., nonmelanoma skin cancers, soft tissue sarcomas, thyroid cancer), as well as ovarian failure, late-onset anthracycline-induced cardiomyopathy, osteoporosis, and overwhelming sepsis caused by splenectomy. Surveillance recommendations, which are available from the Children's Oncology Group screening guideline, are summarized in Table 3.

Final Comments

Definitive recommendations for surveillance of childhood cancer survivors are complicated by published data that generally are limited to cross-sectional studies and cohort studies of limited size. (40) More importantly, the majority of childhood and adolescent survivors present to family physicians at different times in their lives. The intent of the guidelines is to facilitate optimal care of this population and enhance communication between survivors, clinicians, and cancer centers. (43)

Survivors of adult and childhood cancers should be encouraged to engage in preventive health practices, including immunizations, cancer screening, and maintenance of a healthy body weight and balanced nutrition, as well as regular exercise. Physicians should remain alert to nonspecific symptoms or physical findings (e.g., mass, adenopathy) that can indicate cancer recurrence.

The authors indicate that they do not have any conflicts of interest. Sources of funding: none reported.

REFERENCES

(1.) Living beyond cancer: finding a new balance: President's Cancer Panel 2003-2004 annual report. Bethesda, Md.: President's Cancer Panel, National Cancer Institute, National Institutes of Health, U.S. Dept. of Health and Human Services, 2004.

(2.) National Cancer Institute. Surveillance, epidemiology, and end results (SEER). Accessed online September 29, 2004, at: http://www.seer.cancer.gov.

(3.) Brenner H. Long-term survival rates of cancer patients achieved by the end of the 20th century: a period analysis. Lancet 2002;360:1131-5.

(4.) Ogle KS, Swanson GM, Woods N, Azzouz F. Cancer and comorbidity: redefining chronic diseases. Cancer 2000;88:653-63.

(5.) Jeffery GM, Hickey BE, Hider P. Follow-up strategies for patients treated for non-metastatic colorectal cancer. Cochrane Database Syst Rev 2004;(3):CD002200.

(6.) Kattlove H, Winn RJ. Ongoing care of patients after primary treatment for their cancer [published correction appears in CA Cancer J Clin 2003;53:315]. CA Cancer J Clin 2003;53:172-96.

(7.) National Comprehensive Cancer Network. The NCCN clinical practice guidelines in oncology. Accessed online September 29, 2004, at: http://www.nccn.org/professionals/physician_gls.

(8.) Rojas MP, Telaro E, Russo A, Fossati R, Confalonieri C, Liberati A. Follow-up strategies for women treated for early breast cancer. Cochrane Database Syst Rev 2000;(4):CD001768.

(9.) Burstein HJ, Winer EP. Primary care for survivors of breast cancer. N Engl J Med 2000;343:1086-94.

(10.) Fisher B, Jeong JH, Anderson S, Bryant J, Fisher ER, Wolmark N. Twenty-five-year follow-up of a randomized trial comparing radical mastectomy, total mastectomy, and total mastectomy followed by irradiation. N Engl J Med 2002;347:567-75.

(11.) Osuch JR. Breast health and disease over a lifetime. Clin Obstet Gynecol 2002;45:1140-61.

(12.) Schagen SB, van Dam FS, Muller MJ, Boogerd W, Lindeboom J, Bruning PF. Cognitive deficits after postoperative adjuvant chemotherapy for breast carcinoma. Cancer 1999;85:640-50.

(13.) Erickson VS, Pearson ML, Ganz PA, Adams J, Kahn KL. Arm edema in breast cancer patients. J Natl Cancer Inst 2001;93:96-111.

(14.) Harris SR, Hugi MR, Olivotto IA, Levine M. Clinical practice guidelines for the care and treatment of breast cancer: 11. Lymphedema. CMAJ 2001;164:191-9.

(15.) Tamoxifen for early breast cancer: an overview of the randomised trials. Early Breast Cancer Trialists' Collaborative Group. Lancet 1998;351:1451-67.

(16.) Love RR, Mazess RB, Barden HS, Epstein S, Newcomb PA, Jordan VC, et al. Effects of tamoxifen on bone mineral density in postmenopausal women with breast cancer. N Engl J Med 1992;326:852-6.

(17.) Baum M, Buzdar A, Cuzick J, Forbes J, Houghton J, Howell A, et al. Anastrozole alone or in combination with tamoxifen versus tamoxifen alone for adjuvant treatment of postmenopausal women with early-stage breast cancer: results of the ATAC (Arimidex, Tamoxifen Alone or in Combination) trial efficacy and safety update analyses. Cancer 2003;98:1802-10.

(18.) Claus EB, Schildkraut JM, Thompson WD, Risch NJ. The genetic attributable risk of breast and ovarian cancer. Cancer 1996;77:2318-24.

(19.) Renehan AG, Egger M, Saunders MP, O'Dwyer ST. Impact on survival of intensive follow up after curative resection for colorectal cancer: systematic review and meta-analysis of randomised trials. BMJ 2002;324:813.

(20.) Byers T, Levin B, Rothenberger D, Dodd GD, Smith RA. American Cancer Society guidelines for screening and surveillance for early detection of colorectal polyps and cancer: update 1997. American Cancer Society Detection and Treatment Advisory Group on Colorectal Cancer. CA Cancer J Clin 1997;47:154-60.

(21.) Chau I, Allen MJ, Cunningham D, Norman AR, Brown G, Ford HE, et al. The value of routine serum carcino-embryonic antigen measurement and computed tomography in the surveillance of patients after adjuvant chemotherapy for colorectal cancer. J Clin Oncol 2004;22:1420-9.

(22.) Miller AR, Martenson JA, Nelson H, Schleck CD, Ilstrup DM, Gunderson LL, et al. The incidence and clinical consequences of treatment-related bowel injury. Int J Radiat Oncol Biol Phys 1999;43:817-25.

(23.) Penson RT, Gallagher J, Gioiella ME, Wallace M, Borden K, Duska LA, et al. Sexuality and cancer: conversation comfort zone. Oncologist 2000;5:336-44.

(24.) Burt RW. Familial risk and colon cancer. Int J Cancer 1996;69:44-6.

(25.) Lynch HT, Smyrk T, Lynch J. An update of HNPCC (Lynch syndrome). Cancer Genet Cytogenet 1997;93:84-99.

(26.) Dunlop MG, Farrington SM, Carothers AD, Wyllie AH, Sharp L, Burn J, et al. Cancer risk associated with germline DNA mismatch repair gene mutations. Hum Mol Genet 1997;6:105-10.

(27.) Baron JA, Cole BF, Sandler RS, Haile RW, Ahnen D, Bresalier R, et al. A randomized trial of aspirin to prevent colorectal adenomas. N Engl J Med 2003;348:891-9.

(28.) Sandler RS, Halabi S, Baron JA, Budinger S, Paskett E, Keresztes R, et al. A randomized trial of aspirin to prevent colorectal adenomas in patients with previous colorectal cancer [published correction appears in N Engl J Med 2003;348:1939]. N Engl J Med 2003;348:883-90.

(29.) Polascik TJ, Oesterling JE, Partin AW. Prostate specific antigen: a decade of discovery--what we have learned and where we are going. J Urol 1999;162:293-306.

(30.) D'Amico AV, Chen MH, Roehl KA, Catalona WJ. Preoperative PSA velocity and the risk of death from prostate cancer after radical prostatectomy. N Engl J Med 2004;351:125-35.

(31.) Steineck G, Helgesen F, Adolfsson J, Dickman PW, Johansson JE, Norlen BJ, et al. Quality of life after radical prostatectomy or watchful waiting. N Engl J Med 2002;347:790-6.

(32.) Incrocci L, Hop WC, Slob AK. Efficacy of sildenafil in an open-label study as a continuation of a double-blind study in the treatment of erectile dysfunction after radiotherapy for prostate cancer. Urology 2003;62:116-20.

(33.) Chun TY. Coincidence of bladder and prostate cancer. J Urol 1997;157:65-7.

(34.) Steinberg GD, Carter BS, Beaty TH, Childs B, Walsh PC. Family history and the risk of prostate cancer. Prostate 1990;17:337-47.

(35.) Hudson MM, Mertens AC, Yasui Y, Hobbie W, Chen H, Gurney JG, et al. Health status of adult long-term survivors of childhood cancer: a report from the Childhood Cancer Survivor Study. JAMA 2003;290:1583-92.

(36.) Mertens AC, Yasui Y, Neglia JP, Potter JD, Nesbit ME Jr, Ruccione K, et al. Late mortality experience in five-year survivors of childhood and adolescent cancer: the Childhood Cancer Survivor Study. J Clin Oncol 2001;19:3163-72.

(37.) Oeffinger KC, Eshelman DA, Tomlinson GE, Buchanan GR, Foster BM. Grading of late effects in young adult survivors of childhood cancer followed in an ambulatory adult setting. Cancer 2000;88:1687-95.

(38.) Yeazel MW, Oeffinger KC, Gurney JG, Mertens AC, Hudson MM, Emmons KM, et al. The cancer screening practices of adult survivors of childhood cancer: a report from the Childhood Cancer Survivor Study. Cancer 2004;100:631-40.

(39.) Oeffinger KC, Hudson MM. Long-term complications following childhood and adolescent cancer: foundations for providing risk-based health care for survivors. CA Cancer J Clin 2004;54:208-36.

(40.) Oeffinger KC, Eshelman DA, Tomlinson GE, Tolle M, Schneider GW. Providing primary care for long-term survivors of childhood acute lymphoblastic leukemia. J Fam Pract 2000;49:1133-46.

(41.) Bhatia S, Yasui Y, Robison LL, Birch JM, Bogue MK, Diller L, et al. High risk of subsequent neoplasms continues with extended follow-up of childhood Hodgkin's disease: report from the Late Effects Study Group. J Clin Oncol 2003;21:4386-94.

(42.) Bhatia S, Robison LL, Oberlin O, Greenberg M, Bunin G, Fossati-Bellani F, et al. Breast cancer and other second neoplasms after childhood Hodgkin's disease. N Engl J Med 1996;334:745-51.

(43.) Oeffinger KC, Mertens AC, Hudson MM, Gurney JG, Casillas J, Chen H, et al. Health care of young adult survivors of childhood cancer: a report from the Childhood Cancer Survivor Study. Ann Fam Med 2004;2:61-70.

ANNETTE Y. SUNGA, M.D., M.P.H., is a member of the medical staff at the Roswell Park Cancer Institute. She completed a residency in family medicine through the St. John Hospital and Medical Center in Detroit, and received specialized training in cancer prevention and control as part of a general preventive medicine residency program at the State University of New York (SUNY), Buffalo.

MARGARET M. EBERL, M.D., is enrolled in the cancer prevention and control track of the preventive medicine residency at SUNY, Buffalo. She received her medical degree and completed residency training in family medicine at SUNY, Buffalo.

KEVIN C. OEFFINGER, M.D., is professor in the Family and Community Medicine and Pediatrics departments and director of the After the Cancer Experience (ACE) Young Adult Program at the University of Texas Southwestern Medical Center in Dallas. He received his medical degree from the University of Texas Health Science Center in San Antonio, and completed a family medicine residency at the McLennan County Family Practice Residency Program, Waco, Tex.

MELISSA M. HUDSON, M.D., is director of the After Completion of Therapy Clinic and a member in the Hematology/Oncology department at St. Jude Children's Research Hospital in Memphis. She obtained her medical degree and completed pediatric residency training at the University of Texas Medical School in Houston and a pediatric hematology-oncology fellowship at the M.D. Anderson Cancer Center in Houston.

MARTIN C. MAHONEY, M.D., PH.D., F.A.A.F.P., is chair of Clinical Prevention at Roswell Park Cancer Institute, Buffalo. He obtained his medical degree and completed a family practice residency and a faculty development fellowship at SUNY, Buffalo.

Address correspondence to Annette Y. Sunga, M.D., M.P.H., Division of Cancer Prevention and Population Services, Roswell Park Cancer Institute-Carlton 307, Elm and Carlton Streets, Buffalo, NY 14263 (e-mail: Annette.Sunga@RoswellPark.org). Reprints are not available from the authors.

COPYRIGHT 2005 American Academy of Family Physicians
COPYRIGHT 2005 Gale Group