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world cancer report - iarc

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TUMOURS ASSOCIATED WITH<br />

HIV/AIDS<br />

Approximately 30-40% of patients with<br />

HIV infection are likely to develop malignancies.<br />

Kaposi sarcoma is the most common<br />

malignancy in patients with HIV infection.<br />

Since no current therapies have proven<br />

curative, both delivery of effective treatment<br />

and maintenance of adequate control<br />

of HIV and other infections remain the<br />

goals of current treatment. Several studies<br />

have shown benefits of highly active<br />

anti-retroviral treatment (HAART) on<br />

Kaposi sarcoma lesions. HAART might be<br />

a useful alternative both to immune<br />

response modifiers during less aggressive<br />

stages of this disease and to systemic<br />

cytotoxic drugs in the long term<br />

maintenance therapy of advanced Kaposi<br />

sarcoma (Tavio M et al., Ann Oncol, 9: 923,<br />

1998; Tirelli U and Bernardi D, Eur J<br />

Cancer, 37: 1320-24, 2001). Liposomal<br />

anthracyclines are considered the standard<br />

treatment for patients with<br />

advanced stages of AIDS-related Kaposi<br />

sarcoma. Concomitant use of both HAART<br />

and haematological growth factors is<br />

needed, with the aim of reducing opportunistic<br />

infections and myelotoxicity.<br />

Non-Hodgkin lymphoma in patients with<br />

HIV infection is about two hundred-fold<br />

more frequent than expected. One feature<br />

of AIDS-non-Hodgkin lymphoma is the<br />

widespread extent of the disease at initial<br />

presentation and the frequency of systemic<br />

B-symptoms (general symptoms<br />

such as night sweats, weight loss, temperature<br />

change). Whether intensive or<br />

conservative chemotherapy regimens are<br />

appropriate is still a matter of controver-<br />

alter gastric acid secretion, elevating gastric<br />

pH, changing the gastric flora and<br />

allowing anaerobic bacteria to colonize<br />

the stomach. These bacteria produce<br />

60 The causes of <strong>cancer</strong><br />

sy. In fact, the poor bone marrow reserve<br />

and underlying HIV immunodeficiency<br />

make the management of systemic non-<br />

Hodgkin lymphoma very difficult. Intensive<br />

chemotherapy regimens may be given to<br />

low or intermediate risk category patients<br />

and conservative chemotherapy regimens<br />

to high or poor risk patients (Spina M et al.,<br />

Ann Oncol, 10: 1271-1286, 1999). The prognosis<br />

of AIDS-non-Hodgkin lymphoma is<br />

very poor.<br />

Hodgkin disease in patients with AIDS carries<br />

a relative risk much lower than that for<br />

non-Hodgkin lymphoma but the histological<br />

subtypes tend to be those with<br />

unfavourable prognosis and the response<br />

rate remains poorer than that of the general<br />

population. Outcome may be improved<br />

by an optimal combination of anti-neoplastic<br />

and HAART to improve control of the<br />

underlying HIV infection. The inclusion of<br />

growth factors may allow the use of higher<br />

doses of the drugs (Vaccher E et al., Eur J<br />

Cancer, 37: 1306-15, 2001)<br />

Cervical intraepithelial neoplasia (CIN) has<br />

been increasingly diagnosed in HIV-infected<br />

women; invasive cervical <strong>cancer</strong> is currently<br />

an AIDS-defining condition. CIN in<br />

HIV-infected women is associated with high<br />

grade histology, more extensive and/or<br />

multifocal disease and disseminated lower<br />

genital tract HPV-related lesions<br />

(Mandelblatt JS et al., AIDS, 6: 173-178,<br />

1992; Robinson W 3 rd, Semin Oncol, 27:<br />

463-470, 2000). Therapeutic recommendations<br />

are the same as for non-HIV-infected<br />

women, because most HIV-infected women<br />

will die from cervical <strong>cancer</strong> rather than<br />

other AIDS-related diseases.<br />

Testicular <strong>cancer</strong> appears to be more frequent<br />

in HIV-seropositive homosexual men<br />

but the risk is not directly related to the<br />

active reductase enzymes that transform<br />

food nitrate into nitrite, an active molecule<br />

capable of reacting with amines, amides<br />

and ureas to produce carcinogenic<br />

Fig. 2.51 Kaposi sarcoma of the skin in a patient<br />

with AIDS. The biopsy (below) reveals the presence<br />

of human herpes virus 8 (HHV-8) in tumour<br />

cell nuclei, demonstrated by immunohistochemistry<br />

(brown colour). Affected individuals are uniformly<br />

co-infected with HIV and HHV-8.<br />

level of immune deficiency. Patients with<br />

HIV infection are offered the standard<br />

chemotherapy, since the majority can be<br />

cured of their tumour and have a good<br />

quality of life (Bernardi D et al., J Clin<br />

Oncol, 13, 2705-2711, 1995).<br />

The spectrum of <strong>cancer</strong>s in patients with<br />

HIV infection may further increase as<br />

these patients survive longer. Based on<br />

advances in current understanding of HIV<br />

viral dynamics and the availability of<br />

newer anti-retroviral therapies, continuation<br />

of HAART with prophylaxis against<br />

opportunistic infections in patients<br />

receiving chemotherapy may significantly<br />

improve treatment outcome.<br />

N-nitroso compounds. H. pylori acts as a<br />

gastric pathogen and thereby mediates a<br />

carcinogenic outcome involving soluble<br />

bacterial products and the inflammatory

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