She was a new patient to me, referred to discuss her
recurrent gynecologic cancer.* Her history dated back more than seven years
prior, when she underwent surgical treatment and was ultimately
diagnosed with stage II uterine cancer. Chemotherapy had not been recommended.
She did get radiotherapy and underwent close follow-up. Five years later she
had moved to annual visits with her oncology team, and all had been optimistic
she was cured.
She came to clinic on a stretcher—unable to sit up, unable
to walk. Her family accompanied her and I was glad to see she was not alone. We
discussed her diagnosis and the extent of her tumor. Although she had a significant
disease burden, I was hopeful. The finding of MMR deficiency meant she was a
candidate for immunotherapy— pembrolizumab. With that she lit up, as did her
family. “Well, that’s the first bit of good news we’ve had in a while!” Having
breathed that collective sigh of relief, she and her sisters told me more about
their family. Although she had never married, she shared a bond with siblings,
nieces, and nephews. It was clear to me that there was no shortage of love for
sure. We made a plan to start immunotherapy once she was better recovered.
She had resided in a rehabilitation center at the time and
was undergoing daily radiation to her spine. Physical therapy was helping,
though, and with time, she was able to sit up. Then one day, she got out of her
chair and experienced intense pain in her leg and almost fell. It turned out
she had fractured her leg— a pathologic fracture due to cancer. She was
admitted then and stabilized with a plan for more RT. Because the radiation
fields being treated were quite extensive (spine, both femurs), we opted not to
start immunotherapy just then. I had hoped to start her as soon as RT finished,
but within a matter of days, she was readmitted to the hospital—this time due
to hypercalcemia. Although stabilized in a relatively short amount of time, the
coming weeks saw her re-admitted multiple times, all due to complications of
her cancer. A CT scan performed during one of her last hospitalizations had demonstrated
diffuse disease progression.
I was on vacation when she last required admission, but when
I got back, she was still in the hospital. Her family had left a message with my
office, asking me to see her. After reviewing what had happened since we last
met, I made my way up to her room. She was asleep, but woke easily. After some
small talk with her and her family, she asked, “What do you think, doc? Do you
think she can get that treatment soon?” she asked.
I hesitated. On the one hand, I desperately wanted her to
get pembrolizumab. Her tumor was telling me it would work. I had personally
seen it work, almost miraculously in a similar patient with endometrial cancer,
also facing a high tumor burden. She deserved this chance to live, and return
to some semblance of a normal life. Who knows? If she had a great response,
perhaps she could walk again!
Even as these thoughts ran through my head, though, I could
no longer ignore her deterioration. Her bones and spine were literally buckling
under the volume of her cancer, and her most recent scans showed that it was
taking over her vital organs. What if pembrolizumab actually made things worse,
or perhaps even killed her from side effects and unintended consequences?
Ultimately, I had to come face to face with what was
obvious. In front of me was someone who was dying and my window to safely
administer pembrolizumab had closed. “Honestly,” I started. “I would love
nothing more than to treat you and to give you a chance to rediscover life. But
I don’t think that’s going to happen and, frankly, treatment would not be safe.
I think you are dying and I think you only have days to weeks left.”
She buckled and began to cry. “I know,” she said. “I’ve
known for a while.” We talked a bit more about where she wanted to live out the
rest of her life. She was scared of pain and of discomfort, and she wanted more
than anything else to go peacefully. We talked about a hospice facility, but
her medical needs were too great. Ultimately we decided that inpatient hospice
on our floor was the best solution. Our team could take care of her, and we
could take care of her family.
In the end, while precision therapy was available, the
window to treatment had closed and my patient did not have the opportunity to
try it. I tried to hide my frustration and anguish from everyone in that room,
but I saw it mirrored back to me in all of the people who loved her. It wasn’t
fair, and even in an era where we celebrate breakthroughs in cancer treatment,
there will still be women and men like this, and we will mourn our inability to
do more.
*Patient details changed to protect privacy.
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