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Clinical Trial
. 2012 Jan 20;30(3):263-7.
doi: 10.1200/JCO.2011.37.1039. Epub 2011 Dec 12.

Treatment of colorectal peritoneal carcinomatosis with systemic chemotherapy: a pooled analysis of north central cancer treatment group phase III trials N9741 and N9841

Jan Franko  1 , Qian Shi, Charles D Goldman, Barbara A Pockaj, Garth D Nelson, Richard M Goldberg, Henry C Pitot, Axel Grothey, Steven R Alberts, Daniel J Sargent
Affiliations
Clinical Trial

Treatment of colorectal peritoneal carcinomatosis with systemic chemotherapy: a pooled analysis of north central cancer treatment group phase III trials N9741 and N9841

Jan Franko et al. J Clin Oncol. .

Abstract

Purpose: Symptoms and complications of metastatic colorectal cancer (mCRC) differ by metastatic sites. There is a paucity of prospective survival data for patients with peritoneal carcinomatosis colorectal cancer (pcCRC). We characterized outcomes of patients with pcCRC enrolled onto two prospective randomized trials of chemotherapy and contrasted that with other manifestations of mCRC (non-pcCRC).

Methods: A total of 2,095 patients enrolled onto two prospective randomized trials were evaluated for overall survival (OS) and progression-free survival (PFS). A Cox proportional hazard model was used to assess the adjusted associations.

Results: The characteristics of the pcCRC group (n = 364) were similar to those of the non-pcCRC patients in median age (63 v 61 years, P = .23), sex (57% males v 61%, P = .23), and performance status (Eastern Cooperative Oncology Group performance status 0 or 1 94% v 96%, P = .06), but differed in frequency of liver (63% v 82%, P < .001) and lung metastases (27% v 34%, P = .01). Median OS (12.7 v 17.6 months, hazard ratio [HR] = 1.3; 95% CI, 1.2 to 1.5; P < .001) and PFS (5.8 v 7.2 months, HR = 1.2; 95% CI, 1.1 to 1.3; P = .001) were shorter for pcCRC versus non-pcCRC. The unfavorable prognostic influence of pcCRC remained after adjusting for age, PS, liver metastases, and other factors (OS: HR = 1.3, P < .001; PFS: HR = 1.1, P = .02). Infusional fluorouracil, leucovorin, and oxaliplatin was superior to irinotecan, leucovorin, and fluorouracil as a first-line treatment among pcCRC (HR for OS = 0.62, P = .005) and non-pcCRC patients (HR = 0.66, P < .001).

Conclusion: pcCRC is associated with a significantly shorter OS and PFS as compared with other manifestations of mCRC. Future trials for mCRC should consider stratifying on the basis of pcCRC status.

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Conflict of interest statement

Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.

Figures

Fig 1.
Fig 1.
Overall survival by peritoneal carcinomatosis colorectal cancer (pcCRC) status.
Fig 2.
Fig 2.
Survival of N9741 (first-line chemotherapy for metastatic colorectal cancer) by regimen used and peritoneal carcinomatosis colorectal cancer (pcCRC) status. Survival of patients with pcCRC was inferior in all chemotherapy arms. (A) infusional fluorouracil, leucovorin, and oxaliplatin; (B) irinotecan, leucovorin, and fluorouracil; (C) irinotecan and oxaliplatin.
Fig A1.
Fig A1.
Survival of N9841 (second-line chemotherapy for metastatic colorectal cancer) by regimen used and peritoneal carcinomatosis colorectal cancer (pcCRC) status. Survival of patients with pcCRC was (A) noninferior in infusional fluorouracil, leucovorin, and oxaliplatin arm and (B) inferior in irinotecan arm.
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