Timeframe for melanoma lymphadenectomy

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Hi, my partner has recently been diagnosed with Stage IV melanoma with 4 x lesions in his brain. As a healthworker myself, I am really struggling to understand how this has happened and was hoping you could provide information about whether the correct pathway/timeframes were followed. 

He had a primary mole excised from his calf in 2017 with negative sentinel node biopsy. He then had regular surveillance under Dermatology at our local hospital every 3 months. 
Last July 22 a palpable lump was found in his groin by the dermatology CNS. It was biopsied - they said the results would take 2 weeks. After a lot of chasing, at 7 weeks (end of Sept) we were told the results confirmed BRAF+ melanoma. He had a Brain MRI which was clear and a full body CT which confirmed intense uptake in a axial lymph node (Sept). 
They told us surgery would be needed to remove the malignant lymph node/s. No discussion of any systemic treatment or drug therapy. Another full-body PET CT in November showed no spread. 
Start December we received the appointment for the lymphadenectomy for February 27th. He only saw the surgeon before this appointment. No other scans or tests were done. No appointment with oncology. 
Had headaches for 3 weeks in leading up to the surgery which we put down to stress/life etc. Had the lymphadenectomy in Feb and when he came home he became extremely unwell with headaches, ataxia, vomiting. Back to A+E and a CT head confirmed 4 brain mets - 1 the largest one he had a craniotomy for 48hours later as it was causing mass effect. Has now had SRS and on ipi/nivo for the rest of the rest. 

After doing a lot of reading, I am confused (angry) as to why it took almost 6 months for the lymphadenectomy to be done as he would have been classed as Stage 3 melanoma from the moment they got the biopsy results. From reading other forum posts, a lot of people appear to be offered drug treatment options for even Stage 2. 
I understand it's in the past and not overly helpful to dwell on what could have been done differently, but I think having more information about if this is a normal timeframe and he was just 'unlucky' would help me deal with the situation. 

Thankyou!

  • A warm welcome to our online community. My name is Gemma, and I am one of the information nurses here at Macmillan. Thank you for getting in touch at this understandably upsetting time.

    As a support line separate to healthcare services, we are only able to provide generalised information, and therefore cannot directly comment on individual cases: However, we really hope the following information is useful in helping you to decide your next steps.

    Melanoma treatment options are usually discussed within the specialist MDT (multi-disciplinary team meeting) in line with the national guidelines, and where relevant with consideration of clinical trials available. It’s unclear from your email when his case was last discussed at his MDT.

    We would encourage your partner to ask for a further consultation with his team, as they are best placed to explain their rationale for the treatment decisions made, and to answer your questions with regards to why oncology was not involved at an earlier timepoint.

    He may decide to contact the hospital PALS (patient advice and liaison service); who can support with information, communication and signposting to other agencies should you decide to raise a concern or complaint.

    A service external to the NHS who can help are the Citizens Advice Bureau.

    If you think it might help to talk things through in more detail, you or your partner would be welcome to call the Macmillan Support Line free on 0808 808 0000.

    Our line is open 7 days a week, 8am – 8pm. You can also email us back and we aim to reply within two working days.