Researchers Propose New Treatment Guidelines for HIV

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 5 No 8
Volume 5
Issue 8

VANCOUVER, BC--The new understanding of the importance of viral dynamics in the progression of HIV infection (see "New Thinking on HIV Progression Leads to New Strategies") has led to new guidelines for deploying drugs now available to treat HIV (a list of available agents is on page 13). Experts now recommend reducing viral load to below detectable limits, as an indication that viral replication has been curtailed as much as possible.

VANCOUVER, BC--The new understanding of the importance of viraldynamics in the progression of HIV infection (see "New Thinkingon HIV Progression Leads to New Strategies") has led to newguidelines for deploying drugs now available to treat HIV (a listof available agents is on page 13). Experts now recommend reducingviral load to below detectable limits, as an indication that viralreplication has been curtailed as much as possible.

This is important for two reasons. The first is to reduce thenumber of new cells being infected and destroyed by HIV. The secondis to spike one of the virus's main weapons: its ability to mutateand become drug-resistant. Less replication means fewer new virions,which means fewer mutants.

In his presentation at the 11th International Conference on AIDS,Paul Volberding, MD, director of the AIDS Program, San FranciscoGeneral Hospital (SFGH), translated this into practical termsas "response-optimized HIV therapy" (see table ).

At SFGH, antiviral treatment is recommended for all patients withviral load greater than 5,000 to 10,000 copies of viral RNA permilliliter of plasma, regardless of CD4 cell count. In those withviral load over 5,000 to 10,000 and CD4 counts of 350 to 500,recommended treatment is two nucleoside analogs plus a proteaseinhibitor, if needed, to reduce viral load to less than 10,000copies/mL.

"If the baseline viral load is 50,000/mL or less, use oftwo nucleoside analogs may lower it to 5,000 to 10,000,"he said. "If viral load is 50,000 to 150,000, you may beable to get down to that threshold by adding a protease inhibitor."

The 5,000 to 10,000 copies/mL guideline was based in part on thelimits of tests used to measure viral load. Newer tests have reducedthat threshold to 100 to 500 copies/mL, and third-generation testsnow used in research detect 10 to 20 copies/mL, allowing testingof the hypothesis that reducing the viral load to below that levelcould result in long-term "cure" of the disease (see"Early Combination Treatment May Provide HIV Control" fora report of ongoing tests of this hypothesis presented in Vancouver).

Recent Videos
Although high grade adverse effects are infrequent among patients undergoing treatment for SCLC, CRS and ICANS may occur in higher frequencies.
Two experts are featured in this series.
Co-hosts Kristie L. Kahl and Andrew Svonavec highlight what to look forward to at the 67th Annual ASH Meeting in Orlando.
4 experts are featured in this series.
Based on a patient’s SCLC subtype, and Schlafen 11 status, patients will be randomly assigned to receive durvalumab alone or with a targeted therapy in the S2409 PRISM trial.
4 experts are featured in this series.
Daniel Peters, MD, aims to reduce the toxicity associated with AML treatments while also improving therapeutic outcomes.
Numerous clinical trials vindicating the addition of immunotherapy to first-line chemotherapy in SCLC have emerged over the last several years.
Patients with AML will experience different toxicities based on the treatment they receive, whether it is intensive chemotherapy or targeted therapy.
A younger patient with AML who is more fit may be eligible for different treatments than an older patient with chronic medical conditions.
Related Content