4.6 Article

Response rates and durability of chemotherapy among 62 patients with metastatic Merkel cell carcinoma

期刊

CANCER MEDICINE
卷 5, 期 9, 页码 2294-2301

出版社

WILEY
DOI: 10.1002/cam4.815

关键词

Chemotherapy; durability of response; Merkel cell carcinoma; metastatic; neuroendocrine tumor; progression-free survival; response rate

类别

资金

  1. National Institutes of Health (NIH) [K24-CA139052, R01-CA162522, R01-CA176841]
  2. Achievement Rewards for College Scientists Foundation Fellowship
  3. David & Rosalind Bloom Endowment for MCC Research
  4. Michael Piepkorn Endowment Fund
  5. UW MCC Patient Gift Fund
  6. Monica Yolles Fund

向作者/读者索取更多资源

Cytotoxic chemotherapy is commonly used to treat advanced Merkel cell carcinoma (MCC). However, its efficacy in distant metastatic MCC patients is unclear, in part because most prior reports aggregated these patients with those receiving adjuvant chemotherapy and combined chemoradiation for whom prognosis and outcomes may differ. In this retrospective study, we analyzed detailed records from 62 patients with distant metastatic MCC treated with cytotoxic chemotherapy. Efficacy outcomes including response rate (RR), durability of response (DOR), progression-free survival (PFS), and overall survival (OS) were evaluated. In this cohort, platinum plus etoposide was the most commonly used first-line regimen (69%). RR to first-line chemotherapy was 55% (34/62) with complete responses (CR) in 13% (8/62) and partial responses (PR) in 42% (26/62) while 6% (4/62) had stable disease and 39% (24/62) had progressive disease. Median PFS was 94days and median OS was 9.5months from start of chemotherapy. Among responding patients (n=34), median PFS was 168days and median DOR was 85days. Among 30 of the 62 patients who received second-line chemotherapy, RR was 23% (7/30; 1 CR, 6 PR), median PFS was 61days, and median DOR was 101days. In summary, first-line chemotherapy is associated with a high RR in metastatic MCC, but responses are typically not durable, and the median PFS is only 3months. These results suggest rapid emergence of chemoresistance in MCC tumors, and may serve as a useful comparator for immunotherapies currently being explored for metastatic MCC.

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