Hi folks
My question is about side effects with Venetoclax and Obinituzumab. I wonder if anyone out there has any insights.
I'm 66, was diagnosed in July 2020. Watch & wait until July 2022. Started Venetoclax and Obinituzumab in New York at Sloan Kettering. I’ve completed the Obinituzumab, and am now on the regular 400mg/day Venetoclax. A few bumps: Obinituzumab infusion reaction that first day, one urinary tract infection that needed to be treated, low hemoglobin that necessitated transfusions, one Covid bout. But overall, I’m now doing really well, hemoglobin back to normal, platelets higher. Feeling much better.
Except one thing. Early in December, my left knee started to flare up. Quite painful. I have a history with this knee, which has a known torn meniscus, so I went to an orthopedist who took xrays (nothing came up with fractures or arthritis) and who’s given me meloxicam to alleviate inflammation and recommended surgery. However, one blood measure is irregular: high Alkaline Phosphatase, which has been identified as coming from bone. As December progressed, my right knee has joined the party, even though I have no history of soreness or injury! The minute I put weight on either knee they get extremely sore, and I have to constantly ice it and either walk with a cane or avoid walking at all.
My CLL specialist/oncologist has recommended an Endocrinologist consult. My research indicates that the cause of the elevated Alkaline Phosphatase could be anything from thyroid conditions, to conditions such as Osteomalacia or Paget’s disease that weaken bones, to bone metastasis or Osteogenic sarcoma (both cancer in bones). I’ve had cat scans and pet scans in the course of my treatment with no indication of secondary cancers.
I’m anxiously awaiting my meeting with the Endocrinologist. In the meantime – any experience with this out there? I know joint pain is a side effect of some of the drugs, seems like it's more of an issue with BTK inhibitors.
Thanks for reading and thanks in advance.