Guest guest Posted May 16, 2004 Report Share Posted May 16, 2004 Also, it is good to keep in mind that with CLL/SNL one can go form a later stage, e.g. lV back to RAI stage 0 with treatment. Dan Hill Staging CLL and SLL, and a couple of other things From everything I've read, CLL and SLL are basically the same thing and are treated in the same way. Dr. Coutre, in his telephone conference lecture, was asked a question about this. He said cells are considered to be leukemic (as in CLL) if they circulate in the blood. Lymphomas stay in the lymph nodes. If you have mutant B cells that fit the profile for CLL wandering around in your peripheral blood, you have CLL. As to staging - and the Rai system has four stages for CLL -- it's important to keep in mind that staging was developed more than three decades ago when doctors had few tools to understand the disease. So they looked for obvious measurable things. While staging remains important, we now have cytogenetic testing such as FISH (flouresence in-situ hybridization), as well as tests for such markers as CD 38 and ZAP-70, that can give us a more detailed account of what to expect. To solely rely on staging is a mistake. This is not your father's CLL (with apology to Oldsmobile.) I also noted a comment, attributed to the MD website, that one has only nine months to live if refractory to fludarabine. I personally don't like one-size-fits-all " time frames, " and, at any rate, there are new treatments that are changing such statistics. With the advent of Campath, patients now have an alternative if fludarabine fails. And there are new frontiers in immunotherapy - read the " round-headed kid " articles at www.clltopics.org -- that could mean avoiding fludarabine and the harsher chemo drugs altogether. We live in interesting times for CLL (remember the old Chinese curse). Arenson 47, dx '03 Stage 2, 8x Rituxan '04, FISH test '04 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2004 Report Share Posted May 16, 2004 You are absolutely right. I posted the comment about 6 - 9 months to live for patients refactory to Fludara. One-size-fits-all time frames don't fit any better than on-size panty hose and that was the point I was trying to make. I took the article from MD to my first appt with Dr Coutre and asked if this applied to my specific case. He said yes that was about what I could expect. Which actually meant 3 - 6 months for me because I had finished Fludara 3 months prior. That was in January of 2000. According to my calendar I've beat the experts odds by 4 years and my last bone marrow biopsy in June 2003 was normal. I have no evidence of Leukemia in my bone marrow. Campath did it for me. After 6 weeks of treatment I had complete response. There are advances being made every day. New drugs being tested, using combinations of drugs that haven't been tried previously and even Green Tea. This disease doesn't have to be a death sentence any longer. My roll model was a elderly gentleman who was my hay broker. I had no idea he had ever been sick. At 75 years old he looked and acted 10 years younger than his years. After I got to oknow him he told me about having Leukemia. You wouldn't know he had ever had a sick day. At one point he was in the hospital and the Dr told his daughter to make his funeral arrangements that Pete wouldn't make it through the night. 13 years later Pete died of a stroke. Time frames like that are only statistical compulations. They have nothing to do with how an individual is going to respond. Campath only gave me a 33% chance, but I figured someone has to make up that 33% and I might as well be one of them. Sue possumfestival <possumfestival@...> wrote: >Snip I also noted a comment, attributed to the MD website, that one has only nine months to live if refractory to fludarabine. I personally don't like one-size-fits-all " time frames, " and, at any rate, there are new treatments that are changing such statistics. With the advent of Campath, patients now have an alternative if fludarabine fails. And there are new frontiers in immunotherapy – read the " round-headed kid " articles at www.clltopics.org -- that could mean avoiding fludarabine and the harsher chemo drugs altogether. We live in interesting times for CLL (remember the old Chinese curse). Arenson 47, dx '03 Stage 2, 8x Rituxan '04, FISH test '04 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2004 Report Share Posted May 16, 2004 Excellent information , Thanks, K. Staging CLL and SLL, and a couple of other things From everything I've read, CLL and SLL are basically the same thing and are treated in the same way. Dr. Coutre, in his telephone conference lecture, was asked a question about this. He said cells are considered to be leukemic (as in CLL) if they circulate in the blood. Lymphomas stay in the lymph nodes. If you have mutant B cells that fit the profile for CLL wandering around in your peripheral blood, you have CLL. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2004 Report Share Posted May 17, 2004 Sue, I like your style!!! I've always figured to be on the right side of the mean, also. Someone has to be - why not me! Bettie P.S. and YOU! :-) Re: Staging CLL and SLL, and a couple of other things You are absolutely right. I posted the comment about 6 - 9 months to live for patients refactory to Fludara. One-size-fits-all time frames don't fit any better than on-size panty hose and that was the point I was trying to make. I took the article from MD to my first appt with Dr Coutre and asked if this applied to my specific case. He said yes that was about what I could expect. Which actually meant 3 - 6 months for me because I had finished Fludara 3 months prior. That was in January of 2000. According to my calendar I've beat the experts odds by 4 years and my last bone marrow biopsy in June 2003 was normal. I have no evidence of Leukemia in my bone marrow. Campath did it for me. After 6 weeks of treatment I had complete response. There are advances being made every day New drugs being tested, using combinations of drugs that haven't been tried previously and even Green Tea. This disease doesn't have to be a death sentence any longer. My roll model was a elderly gentleman who was my hay broker. I had no idea he had ever been sick. At 75 years old he looked and acted 10 years younger than his years. After I got to oknow him he told me about having Leukemia. You wouldn't know he had ever had a sick day. At one point he was in the hospital and the Dr told his daughter to make his funeral arrangements that Pete wouldn't make it through the night. 13 years later Pete died of a stroke. Time frames like that are only statistical compulations. They have nothing to do with how an individual is going to respond. Campath only gave me a 33% chance, but I figured someone has to make up that 33% and I might as well be one of them. Sue possumfestival <possumfestival@...> wrote: >Snip I also noted a comment, attributed to the MD website, that one has only nine months to live if refractory to fludarabine. I personally don't like one-size-fits-all " time frames, " and, at any rate, there are new treatments that are changing such statistics. With the advent of Campath, patients now have an alternative if fludarabine fails. And there are new frontiers in immunotherapy – read the " round-headed kid " articles at www.clltopics.org -- that could mean avoiding fludarabine and the harsher chemo drugs altogether. We live in interesting times for CLL (remember the old Chinese curse). Arenson 47, dx '03 Stage 2, 8x Rituxan '04, FISH test '04 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2004 Report Share Posted May 17, 2004 Its all about attitude. The best medicine in the world won't save you if you don't have the will to fight. My aunt said she was very impressed with my strength and bravery. I told her it has nothing to do with either one. Its all about being scared to death and running for your life. You will do what ever is necessary if you want to live. It was worth every miserable minute of it. All the misery is now just a bad dream. I laugh about power puking and wearing Depends because I was too weak to make it to the toilet in time. My cousin was going through Interfuron treatment at the same time I was going through the worst of my chemo. We had some pretty interesting conversations and made each other laugh a lot. You can't get away with lying to someone who knows, about how wonderful you feel so we reversed it and grossed each other out with side effect stories. The rest of the family didn't get our warped humor but we both came through. If we hadn't laughed we would have had to cry. If you have the choice I suggest laughing even if its at yourself. If you think about it there is really nothing quite as funny as a 48 year old woman smoking pot for nausea and coughing so hard it starts the gag reflex. I took projectile vomiting to a new art form. Needless to say I only tried that once. I have boiled down my experiences to two bits of advice. Do what ever it takes and be nice to nurses because they have needles. Sue bettie grant <bettiejgrant@...> wrote: Sue, I like your style!!! I've always figured to be on the right side of the mean, also. Someone has to be - why not me! Bettie P.S. and YOU! :-) Quote Link to comment Share on other sites More sharing options...
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