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Dive into the research topics where M. Jacob Adams is active.

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Featured researches published by M. Jacob Adams.


Journal of Clinical Oncology | 2004

Cardiovascular Status in Long-Term Survivors of Hodgkin's Disease Treated With Chest Radiotherapy

M. Jacob Adams; Stuart R. Lipsitz; Steven D. Colan; Nancy J. Tarbell; S. Ted Treves; Lisa Diller; Nina Greenbaum; Peter Mauch; Steven E. Lipshultz

PURPOSE Cardiovascular status was assessed in 48 Hodgkins disease (HD) survivors at a median of 14.3 years (range, 5.9 to 27.5 years) after diagnosis because they may be at increased risk for cardiovascular abnormalities. PATIENTS AND METHODS Patients completed the Short-Form 36 quality-of-life instrument and were screened by echocardiography, exercise stress testing, and resting and 24-hour ECG. RESULTS All patients received mediastinal irradiation (median, 40.0 Gy; range, 27.0 to 51.7 Gy) at a median age of 16.5 years (range, 6.4 to 25.0 years). Four patients received an anthracycline. Although every patient described their health as good or better, and none had symptomatic heart disease at screening, all but one had cardiac abnormalities on screening. Restrictive cardiomyopathy was suggested by reduced average left ventricular (LV) dimension (P < .001) and mass (P < .001), without increased LV wall thickness. Significant valvular defects were present in 42%; 75% had conduction defects. One survivor developed complete heart block shortly after the study visit. Autonomic dysfunction was suggested by a monotonous heart rate in 57%, persistent tachycardia in 31%, and blunted hemodynamic responses to exercise in 27%. Peak oxygen uptake (VO2max) during exercise, a predictor of mortality in heart failure, was significantly reduced (< 20 mL/kg/m2) in 30% of survivors. VO2max was correlated with increasing fatigue, increasing shortness of breath (both, r = -0.35; P =. 02), and decreasing physical component score on the SF-36 (r = 0.554; P = .00017). CONCLUSION A variety of unsuspected, clinically significant cardiovascular abnormalities are common in long-term survivors of HD who are treated at a young age with mediastinal irradiation. We recommend serial, comprehensive cardiac screening of HD survivors who fit this profile.


Critical Reviews in Oncology Hematology | 2003

Radiation-associated cardiovascular disease

M. Jacob Adams; Patricia H. Hardenbergh; Louis S. Constine; Steven E. Lipshultz

As the number of cancer survivors grows because of advances in therapy, it has become more important to understand the long-term complications of these treatments. This article presents the current knowledge of adverse cardiovascular effects of radiotherapy to the chest. Emphasis is on clinical presentations, recommendations for follow-up, and treatment of patients previously exposed to irradiation. Medline literature searches were performed, and abstracts related to this topic from oncology and cardiology meetings were reviewed. Potential adverse effects of mediastinal irradiation are numerous and can include coronary artery disease, pericarditis, cardiomyopathy, valvular disease and conduction abnormalities. Damage appears to be related to dose, volume and technique of chest irradiation. Effects may initially present as subclinical abnormalities on screening tests or as catastrophic clinical events. Estimates of relative risk of fatal cardiovascular events after mediastinal irradiation for Hodgkins disease ranges between 2.2 and 7.2 and after irradiation for left-sided breast cancer from 1.0 to 2.2. Risk is life long, and absolute risk appears to increase with length of time since exposure. Radiation-associated cardiovascular toxicity may in fact be progressive. Long-term cardiac follow-up of these patients is therefore essential, and the range of appropriate cardiac screening is discussed, although no specific, evidence-based screening regimen was found in the literature.


Pediatrics | 2008

Monitoring for Cardiovascular Disease in Survivors of Childhood Cancer: Report From the Cardiovascular Disease Task Force of the Children's Oncology Group

Sadhna M. Shankar; Neyssa Marina; Melissa M. Hudson; David C. Hodgson; M. Jacob Adams; Wendy Landier; Smita Bhatia; Kathleen Meeske; Ming-Hui Chen; Karen E. Kinahan; Julia Steinberger; David N. Rosenthal

Curative therapy for childhood cancer has improved significantly in the last 2 decades such that, at present, ∼80% of all children with cancer are likely to survive ≥5 years after diagnosis. Prevention, early diagnosis, and treatment of long-term sequelae of therapy have become increasingly more significant as survival rates continue to improve. Cardiovascular disease is a well-recognized cause of increased late morbidity and mortality among survivors of childhood cancer. The Childrens Oncology Group Late Effects Committee and Nursing Discipline and Patient Advocacy Committee have recently developed guidelines for follow-up of long-term survivors of pediatric cancer. A multidisciplinary task force critically reviewed the existing literature to evaluate the evidence for the cardiovascular screening recommended by the Childrens Oncology Group guidelines. In this review we outline the clinical manifestations of late cardiovascular toxicities, suggest modalities and frequency of monitoring, and address some of the controversial and unresolved issues regarding cardiovascular disease in childhood cancer survivors.


Circulation | 2013

Long-term Cardiovascular Toxicity in Children, Adolescents, and Young Adults Who Receive Cancer Therapy: Pathophysiology, Course, Monitoring, Management, Prevention, and Research Directions A Scientific Statement From the American Heart Association

Steven E. Lipshultz; M. Jacob Adams; Steven D. Colan; Louis S. Constine; Eugene H. Herman; Daphne T. Hsu; Melissa M. Hudson; Leontien C. M. Kremer; David C. Landy; Tracie L. Miller; Kevin C. Oeffinger; David N. Rosenthal; Craig Sable; Stephen E. Sallan; Gautam K. Singh; Julia Steinberger; Thomas R. Cochran; James D. Wilkinson

Cancer is diagnosed in >12 000 children and adolescents in the United States each year.1 Progress in cancer therapeutics over the past 40 years has remarkably improved survival rates for most childhood malignancies. For all pediatric cancers, 5-year survival increased from 58% for children diagnosed between 1975 and 1977 to 82% for those diagnosed between 1999 and 2006.2 In the United States, this success translates into >325 000 survivors of childhood cancer, of whom 24% are now >30 years from diagnosis.3 During this same period, the incidence of many histological subtypes of childhood cancer has increased, including acute lymphoblastic leukemia (ALL), acute myeloid leukemia, non-Hodgkin lymphoma, neuroblastoma, and soft-tissue and germ-cell tumors.3 Consequently, the number of childhood cancer survivors is expected to increase as a result of the rising pediatric cancer incidence and improved long-term survival rates.3 The increasing number of survivors soon revealed acute and delayed modality-specific toxicities and their impact on quality of life and early mortality. In their seminal 1974 publication, Meadows and D’Angio4 described the wide array of potential late effects of successful therapy for childhood cancer. In the past 2 decades, the Childhood Cancer Survivor Study has also improved our understanding of the long-term mortality and morbidity in this high-risk population. Among young adult survivors of childhood cancer diagnosed between 1970 and 1986, at least 1 of 6 domains of health status (general health, mental health, functional status, activity limitations, cancer-related pain, and cancer-related anxiety) declined moderately to severely in 44%.5 The cumulative incidence of a chronic health condition 30 years after cancer diagnosis is now 73%, with a cumulative incidence of 42% for severe, disabling, or life-threatening conditions or death attributable to a chronic condition.6 Also by 30 years after cancer diagnosis, the cumulative mortality rate from causes …


Pediatric Blood & Cancer | 2005

Pathophysiology of anthracycline- and radiation-associated cardiomyopathies: Implications for screening and prevention

M. Jacob Adams; Steven E. Lipshultz

Great progress has been made in treating childhood cancers over the past 40 years. Along with second malignancies, a major complication of anti‐cancer therapies is adverse cardiovascular effects, especially cardiomyopathy and coronary artery disease. The pathophysiology and characteristics of cardiomyopathy associated with radiation therapy and anthracycline therapy are distinctive. We describe each type of cardiomyopathy, along with its risk factors. These distinctive cardiomyopathies require different screening tests. Appropriate screening of the entire cardiovascular system should be performed because radiation and chemotherapy affect the entire system. Prevention recommendations focus on cardiomyopathy and coronary artery disease. Pediatr Blood Cancer 2005;44:600–606.


Seminars in Radiation Oncology | 2003

Radiation-associated cardiovascular disease: Manifestations and management

M. Jacob Adams; Steven E. Lipshultz; Cindy L. Schwartz; Luis F. Fajardo; Veronique Coen; Louis S. Constine

Irradiation of the heart incidental to the treatment of malignancies can cause a spectrum of cardiovascular complications. These include pericarditis, myocardial fibrosis, muscular dysfunction, valvular abnormalities, and conduction disturbances. Survivors of Hodgkins disease and breast cancer survivors treated with radiotherapy after mastectomy appear to be the groups at highest risk for radiation-associated cardiovascular disease. Although modern techniques of chest radiotherapy have decreased its frequency by reducing the dose and volume of radiation exposure to the heart, survivors treated with radiation remain at increased risk of cardiovascular disease. The risk of fatal cardiovascular disease increases with younger age at treatment, longer follow-up, and higher dose volumes of exposure to the heart. Certain chemotherapeutic agents, such as anthracyclines, also increase the risk of damage to the heart. Cardiac damage associated with radiotherapy may be progressive. Screening of survivors may help identify those at highest risk for serious cardiovascular disease. The broad range of radiation-associated cardiovascular disease makes it necessary for survivors to be examined with multiple screening modalities, although data do not exist to support definitive recommendations on test frequency.


Cancer | 2009

The effect of modafinil on cognitive function in breast cancer survivors

Sadhna Kohli; Susan G. Fisher; Yolande Tra; M. Jacob Adams; Mark Mapstone; Keith Wesnes; Joseph A. Roscoe; Gary R. Morrow

The authors conducted a randomized clinical trial examining the effects of modafinil in reducing persistent fatigue in patients after treatment for cancer and performed secondary analyses to assess the effect of modafinil on cognitive function.


Journal of Clinical Oncology | 2010

Cardiotoxicity after childhood cancer: Beginning with the end in mind

Steven E. Lipshultz; M. Jacob Adams

Worldwide, more than 28 million people live with cancer. This number could triple by 2030. With the increasing number of patients with cancer and improvements in cancer management that continue to reduce cancer death rates, the number of cancer survivors is projected to increase rapidly, in particular, those afflicted during childhood. In children and adolescents, the survival rate has jumped from fewer than 50% in the mid-1970s to 80% today. The growing population of childhood survivors is notable for its vulnerability to adverse health outcomes, many of which may not become clinically apparent until years after the completion of therapy. Despite surviving their initial cancer, childhood cancer survivors continue to face considerable premature mortality as adults. The excess risk of dying from other causes that contributes most to loss of life expectancy is the increased incidence of chronic conditions among survivors of childhood cancer. We need to monitor the health of these survivors and to minimize the use of therapies with late toxicities in newly diagnosed patients. Survivors also experience a higher prevalence of chronic conditions, with as many as two thirds of childhood cancer survivors reporting at least one chronic condition and one fourth reporting a severe, disabling, or life-threatening condition. Survivors of childhood cancer are 5 to 10 times more likely than their healthy siblings to experience heart disease. The incidence of these conditions increases with time, so the full extent of disease- and treatment-related late effects has yet to be realized. Survivors of childhood cancer are a new, large, emerging population at risk for acquired premature symptomatic cardiovascular disease. The report by Tukenova et al 1 provides important information on late excess cardiovascular mortality in childhood cancer survivors and on the factors associated with this mortality. Their report adds new information about late cardiac effects in childhood cancer survivors by specifically using carefully calculated radiation doses to the heart as a factor to assess overall mortality and cardiovascular mortality. Importantly, this study also evaluated the potential classes of medications for their association with cardiovascular mortality. This article not only validates previous studies of overall cardiac mortality, 2-7 it also provides new data on cumulative anthracycline dose, cumulative radiation dose, and the contribution of other agents. Although the dose-dependent risk of congestive heart failure and related deaths associated with anthracyclines among childhood cancer survivors is established, and although radiation exposure to the heart has also been associated with increased risk of cardiovascular disease, this article’s evaluation of the association between the dose of radiation and the dose of anthracyclines on cardiovascular mortality in the same cohort is important. Studies have generally looked only at radiation as a dichotomous variable, although others have looked at treat


Journal of Clinical Oncology | 2012

Cardiovascular Status of Childhood Cancer Survivors Exposed and Unexposed to Cardiotoxic Therapy

Steven E. Lipshultz; David C. Landy; Gabriela Lopez-Mitnik; Stuart R. Lipsitz; Andrea S. Hinkle; Louis S. Constine; Carol A. French; Amy M. Rovitelli; Cindy Proukou; M. Jacob Adams; Tracie L. Miller

PURPOSE To determine whether cardiovascular abnormalities in childhood cancer survivors are restricted to patients exposed to cardiotoxic anthracyclines and cardiac irradiation and how risk factors for atherosclerotic disease and systemic inflammation contribute to global cardiovascular status. METHODS We assessed echocardiographic characteristics and atherosclerotic disease risk in 201 survivors of childhood cancer with and without exposure to cardiotoxic treatments at a median of 11 years after diagnosis (range, 3 to 32 years) and in 76 sibling controls. RESULTS The 156 exposed survivors had below normal left ventricular (LV) mass, wall thickness, contractility, and fractional shortening and above normal LV afterload. The 45 unexposed survivors also had below normal LV mass overall, and females had below normal LV wall thickness. Exposed and unexposed survivors, compared with siblings, had higher levels of N-terminal pro-brain natriuretic peptide (81.7 and 69.0 pg/mL, respectively, v 39.4 pg/mL), higher mean fasting serum levels of non-high-density lipoprotein cholesterol (126.5 and 121.1 mg/dL, respectively, v 109.8 mg/dL), higher insulin levels (10.4 and 10.5 μU/mL, respectively, v 8.2 μU/mL), and higher levels of high-sensitivity C-reactive protein (2.7 and 3.1 mg/L, respectively, v 0.9 mg/L; P < .001 for all comparisons). Age-adjusted, predicted-to-ideal 30-year risk of myocardial infarction, stroke, or coronary death was also higher for exposed and unexposed survivors compared with siblings (2.16 and 2.12, respectively, v 1.70; P < .01 for both comparisons). CONCLUSION Childhood cancer survivors not receiving cardiotoxic treatments nevertheless have cardiovascular abnormalities, systemic inflammation, and an increased risk of atherosclerotic disease. Survivorship guidelines should address cardiovascular concerns, including the risk of atherosclerotic disease and systemic inflammation, in exposed and unexposed survivors.


Radiation Research | 2012

A Pooled Analysis of Thyroid Cancer Incidence Following Radiotherapy for Childhood Cancer

Lene H. S. Veiga; Jay H. Lubin; Harald Anderson; Florent de Vathaire; Margaret A. Tucker; Parveen Bhatti; Arthur B. Schneider; Robert Johansson; Peter D. Inskip; Ruth A. Kleinerman; Roy E. Shore; Linda Pottern; Erik Holmberg; Mike Hawkins; M. Jacob Adams; Siegal Sadetzki; Marie Lundell; Ritsu Sakata; Lena Damber; Gila Neta; Elaine Ron

Childhood cancer five-year survival now exceeds 70–80%. Childhood exposure to radiation is a known thyroid carcinogen; however, data are limited for the evaluation of radiation dose-response at high doses, modifiers of the dose-response relationship and joint effects of radiotherapy and chemotherapy. To address these issues, we pooled two cohort and two nested case-control studies of childhood cancer survivors including 16,757 patients, with 187 developing primary thyroid cancer. Relative risks (RR) with 95% confidence intervals (CI) for thyroid cancer by treatment with alkylating agents, anthracyclines or bleomycin were 3.25 (0.9–14.9), 4.5 (1.4–17.8) and 3.2 (0.8–10.4), respectively, in patients without radiotherapy, and declined with greater radiation dose (RR trends, P = 0.02, 0.12 and 0.01, respectively). Radiation dose-related RRs increased approximately linearly for <10 Gy, leveled off at 10–15-fold for 10–30 Gy and then declined, but remained elevated for doses >50 Gy. The fitted RR at 10 Gy was 13.7 (95% CI: 8.0–24.0). Dose-related excess RRs increased with decreasing age at exposure (P < 0.01), but did not vary with attained age or time-since-exposure, remaining elevated 25+ years after exposure. Gender and number of treatments did not modify radiation effects. Thyroid cancer risks remained elevated many decades following radiotherapy, highlighting the need for continued follow up of childhood cancer survivors.

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Stuart R. Lipsitz

Brigham and Women's Hospital

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