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Case report and review of primary cervical melanoma shows inconsistent response to PD-1/PD-L1 inhibitors

Case report and review of primary cervical melanoma shows inconsistent response to PD-1/PD-L1 inhibi…
Photo by Navy Medicine / Unsplash
Key Takeaway
Note: Evidence for treating primary cervical melanoma is limited to case reports with inconsistent immunotherapy response.

This publication presents a case report of two patients with primary malignant melanoma of the cervix (PMMC) and a systematic review of nine reported cases treated with PD-1/PD-L1 inhibitors. The first patient underwent radical surgery without adjuvant therapy and died from recurrence 36 months later. The second patient, treated with radical surgery, adjuvant chemotherapy, bevacizumab maintenance, and a combination of carboplatin, dacarbazine, and Tislelizumab, showed significant tumor regression after two cycles.

The literature review found that radical surgery was performed in 90% of patients, while 80% did not receive chemotherapy or radiotherapy. Notably, 80% of patients experienced disease progression despite immunotherapy. PD-L1 expression was assessed in only three cases and was negative in all, not reliably predicting response.

Safety and tolerability data for the treatments were not reported. Key limitations include the exceptionally rare nature of the disease, the lack of standardized treatment guidelines, and inconsistent response to immune checkpoint inhibitors. High recurrence rates were observed despite surgery.

Given the formidable clinical challenge of PMMC, multimodal strategies integrating surgery, chemotherapy, anti-angiogenic agents, and immunotherapy may offer clinical benefit. However, the evidence is based on a handful of cases, and the efficacy of immunotherapy appears limited in most instances, necessitating a highly cautious and individualized approach.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMar 2026
View Original Abstract ↓
Primary malignant melanoma of the cervix (PMMC) is an exceptionally rare and aggressive malignancy with a poor prognosis. Due to its rarity, there are no standardized treatment guidelines. This case report presents two patients with PMMC, contributing to the literature through a novel treatment approach and literature review. Both patients presented with vaginal bleeding: one postmenopausal without obvious cervical pigmentation, the other premenopausal with a brown, friable cervical mass. Histopathology confirmed PMMC in both. The first patient underwent radical surgery without adjuvant therapy and died from recurrence 36 months later. The second patient received radical surgery, adjuvant chemotherapy, and bevacizumab maintenance, followed by a combination of carboplatin, dacarbazine, and Tislelizumab for pulmonary metastases, achieving significant tumor regression after two cycles. A review of nine reported cases treated with PD-1/PD-L1 inhibitors revealed that radical surgery was performed in 90% of patients, yet 80% did not receive chemotherapy or radiotherapy, and most (80%) still experienced disease progression with immunotherapy, underscoring its limited efficacy. PD-L1 expression, assessed in only three cases (all negative), did not reliably predict response. In conclusion, PMMC remains a formidable clinical challenge with high recurrence rates despite surgery. Response to immune checkpoint inhibitors is inconsistent, but multimodal strategies integrating surgery, chemotherapy, anti-angiogenic agents, and immunotherapy may offer clinical benefit and warrant further investigation to improve outcomes in this aggressive disease.
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