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Temador, anyone?
I know I have already heard from some, but I can't find postings from everyone who has had an experience with Temador for brain mets...
If you have taken it or are taking it, please let me know. I need to include this info in my research paper that I am preparing for my meeting with my onc tomorrow... And please tell me what other chemos, monoclonals (Herc or Ty?), or treatments (rads? WBR or targeted?) that you were on at the same time. Thanks!! |
Brenda,
I'm afraid this is too late for you, but here goes anyway... I'm pasting something you could print out for your docs. I don't know anyone on this site who has also been on Temodar, except perhaps Barbara H/ in Houston? I get them mixed up, and I apologize...... ok, here's the info: SABCS ABSTRACT: [San Antonio Breast Cancer Symposium] [1079] Phase I study of capecitabine (C) in combination with temozolomide (T) in the treatment of patients with brain metastases from breast carcinoma. Rivera E, Valero V, Francis D, Brewster A, Royce M, Esteva F, Murray JL, Pusztai L, Hortobagyi GN.. The University of Texas M.D. Anderson Cancer Center, Houston, TX Background: T is an oral alkylating agent that is currently being used for the treatment of primary brain tumors due to its ability to cross the blood-brain barrier. C has been approved for use in the treatment of metastatic breast cancer patients who have failed anthracyclines and taxanes. It is well known that C crosses the blood-brain barrier and has activity in the brain. Options are limited for patients with brain metastases. Materials and Methods: We evaluated the activity of both drugs in combination for the treatment of brain metastases not amenable to surgery. Patients were allowed in the study if they had new onset brain metastases from breast cancer, had declined radiation therapy, and were neurologically stable. They were also eligible if they had evidence of recurrence or progression of brain metastases after whole brain or stereotactic radiation therapy. C was started at 1800 mg/m2 in 2 divided doses. T was given at a starting dose of 75 mg/m2 in one daily dose. Each drug was given concomitantly every day for 5 days (day 1-5) followed by 2 days of rest and restarted again for an additional 5 days (days 8-12). Each cycle was repeated every 21 days. We have enrolled a total of 16 pts — 6 pts at dose level 0 (C/T — 1800/75), 6 pts at dose level 1 (C/T — 1800/100), and 4 pts at dose level 2 (C/T — 2000/100). Results: Five pts had recurrent brain metastases and had been previously treated with radiation therapy. The median age is 51 yrs (range, 32-77). All pts had a Zubrod performance status < 1. Ten pts were ER and/or PR positive. No grade 4 toxicities have been reported. Grade 3 toxicity includes headaches (2 pts), vomiting (1 pt), constipation (2 pts), fatigue (2 pts), nonneutropenic fever (1 pt). We have observed 1 CR, 1 PR, 6 MR, and 3 SD. Four pts did not respond to treatment. One pt was not evaluable for response. Median duration of response in brain was 10.5 weeks (range, 6-48+ wks). Two pts with SD and 2 pts with MR had previously received whole brain radiation therapy. Three pts were taken off the study because of progression of disease outside the brain including the pt who had a CR in brain but progressed systemically. Four pts are actively being treated in the study. Conclusions: The combination of C and T seems to be active and well tolerated for the treatment of brain metastases from breast carcinoma. Further studies should include the evaluation of this combination with radiation and as adjuvant therapy in those pts who are at high risk of developing brain metastases. Wednesday, December 8, 2004 4:30 PM Poster Session: Treatment: Chemotherapy -- New Drugs and Formulations (4:30 PM-7:00 PM) Best of luck, pattyz |
Not too late at all Patty - appt isn't until this afternoon... thanks!!
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oh! I'm so glad to see this. Hope it helped, then.
hugs, patty |
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