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AIDS Treatment News
Treatment Interruptions Dr. Cohen: There were a couple of very important presentations on treatment interruptions [see abstracts #64 through #68lb on this topic]. I would summarize them as follows: We continue to learn from studies that in some cases people can safely stop their medications. If somebody has had a good CD4 rise and then stops medication, CD4 counts do not plummet rapidly, on average. The viral load, even as it goes up, may leave most people able to tolerate some time off antiretrovirals if that is their choice. The risks include a few percent who can have symptoms associated with HIV rebound -- similar to what some have when first exposed to HIV. We have also learned at past meetings that the other risk of stopping -- rapidly falling CD4 counts -- is greatest in those who have a history of very low counts -- suggesting that immune reconstitution is not always complete for those who have ever had very low CD4 counts. But even this is a generalization -- there are some with low counts in the past who have stopped and had some time off with stable counts -- they just need more frequent monitoring if they do stop. New data at this meeting highlighted a caution -- that a few percent of people will develop viral resistance when stopping antiretrovirals. Understanding of why and when that happens is still evolving. But it appears that if your viral load is higher than 50 and you stop your antiretrovirals, that is when you are more likely to develop resistance. And this resistance is most likely to drugs with a "low genetic barrier" to the development of resistance - especially 3TC and the non-nukes [efavirenz and nevirapine].
 We are
seeing results of studies showing that people can take weeks or even months
off antiretrovirals (long-cycle approaches to treatment interruption). For
example, a Thai trial compared short treatment cycles (7 days on and 7 days
off), vs. continuous treatment, vs. a strategy of stopping when the CD4
counts are above 350 and starting only after a 30% drop in the counts.(1)
The researchers noted that their volunteers needed to be on medications
only 33% of the time with this CD4-guided strategy. This approach is promising
to reduce drug exposure. And it is similar to the strategy being tested
in the international "SMART" trial -- the largest trial ever attempted in
our field. (SMART compares long-cycle interruptions to continuous therapy.
It is tackling a key issue in structured treatment interruption, which is
whether it makes a difference in the long term. Readers can learn more about
the SMART study at http://www.smart-trial.org
)
But an important caution about treatment interruption also came from this trial,(1) which showed that the 7-day-on-7-day-off antiretroviral regimen for people with well-suppressed virus did not always work. This trial had 73 volunteers, of whom about a third did 7 days on and 7 days off, and there were virologic escapes. There may be reasons that explain it, including underlying resistance, or these volunteers not always having less than 50 when they stopped. These are just conjectures, as the research team did not fully explain why their results differed so much from other studies that showed successful suppression even after 7 days off. The bottom line is that the 7-7 regimen is still a research approach with rules yet to be understood, which is why we remind people that this is still research and not a recommendation. If everybody looked at the 7- 7 data from Dr. Dybul at the National Institutes of Health and started doing it, the Thai data suggests that as many as half of the people trying it could have virologic escape. Researchers and doctors are cautious because sometimes we learn later on that problems occur. We need time and experience to understand the newer strategies in order to know how to apply our findings. So these days if someone is considering a treatment interruption, and they want to be as conservative as possible -- meaning to conserve the drugs they are on now for use next time -- some of the studies suggested treatment interruption may be safe, but it is also important to do so in a way that minimizes creating resistance. Resistance occurs while the drugs are leaving the bloodstream and are present in concentrations too low to stop the virus from growing. So we can take advantage of the higher genetic barrier to resistance of boosted protease inhibitors. One approach I use is a week of boosted dual protease inhibitors to avoid resistance. If someone is on, say, AZT plus 3TC plus efavirenz, I may substitute a dual boosted protease inhibitor combination, Kaletra plus saquinavir, for example, for a week. This allows the AZT, 3TC, and efavirenz to leave the bloodstream while continuing viral suppression. Then you can stop the protease inhibitors, and these drugs have a high enough genetic barrier that you are quite unlikely to lose them to resistance. Otherwise, you might lose 3TC or efavirenz - - and it seems to me a good use of that week on an alternative regimen to not risk losing those very precious drugs. Get them out of your system while the virus is suppressed. James: As a practical matter, do you have trouble with reimbursement if you prescribe these drugs for just one week?
Dr. Cohen: In my experience, no, because it appears the same as
if I am just switching to this combination; no insurance refuses
to pay for medication switches. And certainly our pharmacies
here in Massachusetts are enlightened enough that if I want to
give somebody a week's supply instead of a month's supply they
are OK with that. It may be different elsewhere.
Choosing Drugs for Highly Treatment Experienced Patients ("Deep Salvage") James: What was new at this meeting for people who have had extensive antiretroviral treatment, and have already developed resistance to a number of the drugs? Dr. Cohen: At this meeting we saw two very important pieces of the puzzle. One area is new drugs. Another is an idea on how to wait instead of switching antiretrovirals too soon. Given that there are important new drugs coming, the question is what to do if somebody is on a combination now that is holding them at some acceptable viral load. If they do not have enough new drugs that can work for them to create an effective, potent regimen that makes it likely they will re-establish suppression, we have seen that if you switch too early they will lose those drugs and be back where they started, only worse since they now have even fewer options. So there has always been an interest in postponing the switch until you have a good switch. The difficult question for a couple of years has been, what do you do while you wait? Because keeping someone on a regimen allowing partial suppression, but unfortunately also allowing the virus to create more and more mutations, creates more and more cross resistance, potentially losing options you've been trying to save somebody for. No one has a great answer, but Steve Deeks presented some very preliminary but creative work, that for many was one of the highlights of the meeting for innovativeness.(2) Since after resistance non-nukes are generally useless, he has people on a combination of nucleoside analogs and protease inhibitors, as most of us do. He then focused on a group who were still receiving benefit from the antivirals -- those whose current viral load on meds was lower than their set point -- suggesting that at least some of the meds were working. Then he thought, maybe we could "save" a class -- and keep people on just nucleoside analogs, or just protease inhibitors, minimizing creating more resistance to either one class or the other -- and minimizing toxicity from one class as well. He showed that when he stopped the protease inhibitors, maintaining the nucleosides only, at least for weeks if not months, the viral load stayed suppressed; he could maintain this viral load even without the protease inhibitors for months. Five patients did the reverse, and stayed on the protease inhibitors, and he did see a viral load increase of a little over half a log -- suggesting that, at least for now, stopping the protease inhibitors and maintaining nucleosides may be a better way to postpone switching and preserve the protease inhibitors for the future. If you are off the protease inhibitors you will not develop new PI mutations, so drugs like tipranavir may stay more active for you. That's the logic. Dr. Deeks also pointed out that this approach does not last forever. It may be a stalling maneuver. It does provide food for thought, and maybe another option for a while. But he noted that in time the nucleoside-inhibitor-only approach will lead to rebound -- so it might be necessary to restart the protease inhibitors for some period of time, to take advantage of the fact that the protease inhibitors can reduce the blood level of even resistant virus. The key is to emphasize that these observations are the beginning of a story -- and we have much to learn about when these observations hold true, as well as when we will see different outcomes. But it has some relevance for some people now. There are new drugs coming. We saw data on tipranavir that shows that the company now has a dose worth using, and that it works well against many protease-inhibitor-resistant mutations. T-20 is already well established and approved for sale at least in the U.S. as of March 2003; in this meeting we saw data to show that T-1249 works if you have T-20 resistance, and it works quite well. We also saw data about other new classes of drugs, including many other entry inhibitors, CCR-5 inhibitors, and one drug from a completely new class that may be a viral assembly inhibitor. Many of these new drugs are still only in the test tube; there is a little clinical data. But it was promising that people are finding new drugs and new drug classes that work against resistant viruses. Human Monoclonal Antibody James: What do you think about the early test of the anti-HIV antibody TNX-355 -- a new kind of possible treatment that was injected once, and still inhibited HIV two weeks later?(3) Dr. Cohen: It's not clear ultimately where this drug will go -- but there might be an injectable treatment given every two weeks or so. In the trial so far they gave only one dose, and two weeks later the virus reached its lowest point. We have never before seen a drug that a single dose took two weeks to reach its maximum response; it is not entirely clear why that happened. This finding was curious but suggests that this drug binds to the cells for a prolonged period and maintains the effects for far longer than our usual oral medication. It raises a host of questions because we have not used drugs with these characteristics before. James: Activists were disappointed that there was no human data on TMC125, a new and very powerful non-nucleoside.(4) Dr. Cohen: Yes, there may be issues with the formulation. This drug has been burdened by a formulation that requires many pills per day, and the company is working hard to improve on that before moving ahead. As I understand it, they are closer to proceeding to the next phase of research. There are many drugs we will hear about over time -- some will be developed more slowly than others. We are hearing less data about some potential drugs since many trials are just under way. Because we do not hear about something does not necessarily mean there is no new information about it. Sometimes the trials are being planned or have started, but are not mature enough to be presented at scientific meetings. Summary James: Could you summarize some of your main take-home points from the meeting? Dr. Cohen: (1) We continue to learn that we are far from preventing HIV infection with a vaccine. Therefore prevention through behavior changes that are maintained is critical to protecting oneself reducing the size of the epidemic. We also don't know much more about the risk from re-exposure to HIV, so for now we suggest caution as more is learned. (2) We know that treatment works, and we are learning more about the tradeoffs with different approaches. There is no perfect regimen for everyone, but clearly some choices have well- established advantages over others. (3) We must continue to be vigilant about side effects. While searching for ways to both prevent and reverse them, we must also be alert for newer side effects that we do not yet know much about. We are only six years into the "HAART" era -- and without a cure in place, we have decades to go. (4) Starting treatment is no longer a single decision to be made once -- people can stop and restart multiple times in different patterns. The benefits and risks of these approaches are finally beginning to be defined. And through longer-term studies finally underway, we hope to be able to move from the era of knowing that we can stop medications in some cases, to knowing whether we should stop medications. It will take many people in long- term studies to answer this question. (5) The only way forward is more research. We all need to be vigilant about supporting HIV research, as well as advocating for our own field. References Note: These references are to the 10th Conference on Retroviruses and Opportunistic Infections, Boston February 10- 14, 2003. They are available at http://www.retroconference.org and will remain there for about a year. The abstracts should be readable on all computers, but the browser's Internet security setting should not be too high, or the software to search the abstracts will not work. 1. J Ananworanich, P Cardiello, P Srasuebkul, and others. HIV- NAT 001.4: A Prospective Randomized Trial of Structured Treatment Interruption in Patients with Chronic HIV Infection. [Abstract #64] 2. SG Deeks, JN Martin, R Hoh, T Wrin, C Petropoulos, and RM Grant. Continued reverse transcriptase inhibitor therapy is sufficient to maintain short-term partial suppression of multi- drug resistant viremia. [Abstract #640] 3. DR Kuritzkes, JM Jacobson, W Powderly and others. Safety and preliminary anti-HIV activity of an anti-CD4 mAb (TNX-355; formerly HU5A8) in HIV-infected patients. [Abstract #13] 4. K Das, AD Clark, and PL Boyer. Could multiple modes of binding of a potent NNRTI TMC125-R165335 explain its potency against common drug-resistant mutants? [Abstract #613 - Poster available] AIDS Treatment News Published twice monthly Subscription and Editorial Office: 1233 Locust St., 5th floor Philadelphia, PA 19107 800/TREAT-1-2 toll-free email: aidsnews@critpath.org useful links: http://www.aidsnews.org/ Editor and Publisher: John S. James Associate Editor: Tadd T. Tobias Statement of Purpose: AIDS Treatment News reports on experimental and standard treatments, especially those available now. We interview physicians, scientists, other health professionals, and persons with AIDS or HIV; we also collect information from meetings and conferences, medical journals, and computer databases. Long-term survivors have usually tried many different treatments, and found combinations that work for them. AIDS Treatment News does not recommend particular therapies, but seeks to increase the options available. AIDS Treatment News is published 24 times per year, on the first and third Friday of every month, and print copies are sent by first class mail. Email is available (see below). Back issues are available at http://www.aidsnews.org/ To subscribe, you can call 800-TREAT-1-2 or 415-255-0588: |
Dr. Cal Cohen