One out of eight 8 had a grade 4 hematologic toxicity. 50% of the patients were alive and disease free. However the remaining
four patients died from AIDS related illnesses in the 3 year follow up (40). Around the same time Kim et al (George Washington University, 2001) showed that HIV+ patients had worse outcomes and tolerance than HIV negative patients in the treatment of anal cancer using the standard RT dose of 50-54 Gy and concurrent full dose chemotherapy (6). In this study, analyzed patients were from 1985 to 1998 a period of time before the advent of HAART. The HIV+ patients included patients with AIDS defining illnesses, Inhibitors,research,lifescience,medical and low CD4 counts. These patients tended to have a lower performance status. Inhibitors,research,lifescience,medical Overall 5/13 HIV+ patients analyzed failed initial definitive chemoradiation compared to 9/60 HIV negative patients. If the patients with known AIDS were removed from the analysis, the differences in treatment outcomes between the two groups are reduced. The only patients that required treatment breaks were the patients with AIDS. Each required an unscheduled 3-4 week treatment break due Inhibitors,research,lifescience,medical to grade 4 toxicity (1-skin ulcer, 1-thrombocytopenia). Furthermore, in the Kim analysis, late toxicity
(poor skin healing) was higher in the HIV+ group 4/10 versus 5/33. Another early study also suggested that HIV+ patients with AIDS may not tolerate anal cancer treatment. Clinicians at the Beth Israel Medical Center in NY (1987-1991) commented on the results of treating 9 HIV+ patients, 3 of which had AIDS (41). The authors reported over 50% needed more than 2 weeks of unscheduled treatment break due to toxicity. Over 50% had grade 3-4 skin toxicity. However, 7/9 did have a clinical complete Inhibitors,research,lifescience,medical response despite the toxicity. At least one of the two patients that did not have a complete response also had AIDS. The author do mention that an early antiretroviral, Inhibitors,research,lifescience,medical zidovudine was given concurrently with chemoradiation in patients and was well tolerated. Delineation of subgroups in the HIV+ population can help identify HIV+ patients that may not tolerate treatment from those that can tolerate standard combined modality therapy. In 1999, Hoffman
et al (UCSF) published a report on a small cohort of HIV+ patients treated for anal cancer (42). Hoffman et al (1999) stratified patients based on CD4 count and showed that values greater than 200 Linifanib (ABT-869) portend to superior treatment outcomes and tolerance (42). Patients with higher CD4 counts were more likely to receive the standard of care in terms of chemotherapy and RT dosing. These authors suggested that fear of toxicity caused physicians to empirically alter chemotherapy regimens in the HIV+ population. The mean RT dose was similar between the 2 groups ~51 Gy. However even with an altered chemotherapy http://www.selleckchem.com/products/abt-199.html regimen the group with CD4 counts less than 200 still experienced more toxicity such as moist desquamation and hematologic suppression.