Immunotherapy Scheduling
I am totally new to Keytruda infusions, having only had one a week ago. I was under the impression I'd be routinely scheduled for these infusions every three weeks - on the same day of the week - but to date I've not gotten any information about my next one which ought to be in two weeks on a Wednesday. I've called scheduling twice but have not yet received notification. Is it common to not get notification of the date/time until a few days beforehand?
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@grammato3. yes, if the PET scans every 3_4 months say clear, they tell me 1 1/2 to maybe 2 years of Keytruda. This is due to my melonoma being grade 3C.
@grammato3
Yes, they anticipate 1 1/2 to 2 years of immonutherapy as long as the PET scans remain clear.
Keep us posted on your biopsy!
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1 Reaction@grammato3
Fatigue was more after the first and second infusions. I feel so fortunate to not have experienced a rash, diarrhea, or not keeping food down.
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1 Reaction@mark13903, welcome. Are you being treated for melanoma? How are you doing?
@colleenyoung yes I have stage 4 Malignant melanoma that has Matastsized to my liver, both lungs, 2a cervical, left axillary nodes, baseball size left axillary mass. Braf Negative. I began the Opdualag on Nov 25, 2025 very few side effects. Since beginning my baseball size mass is gone. My next treatment is Dec 23rd... this Tuesday at the Jax facility. Are you also Melanoma positive?
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2 ReactionsI do not have melanoma, however, others here do, like @grammato3.
@mark13903, how did your recent appointment go? How are you doing?
@colleenyoung the staff is great... everything runs like a well oiled machine. Dr Doonan is perfect for my approach to this medical issue. I want direct... but most important he listens intently and truly thinks about my question... before answering. I slept for 2 days after my 2nd infusion. Advill for 7 days... all good.. Opdualag. Thank you for asking.
@mark13903: I also have Stage IV metastatic melanoma and have been treating at the Phoenix location. I recently learned that due to adverse effects I can no longer continue with immunotherapy with had been helpful in resolving my lung nodule. I will post about that after my upcomine PET scan in a couple of weeks.
I'm glad to hear you've been pleased with Dr. Doonan and your care at Jacksonville. Everyone I've come in contact with has had only positive things to stay about the oncology staff at all the Mayo facilities. How do I know this? Because I've been participating in the the Melanoma Support group offered through Mayo since shortly after my diagnosis in November 2024. We meet via Zoom on the second Tuesday of each month. Here's the information: https://connect.mayoclinic.org/events/.
Is that perhaps something you might be interested in?