J Korean Med Sci.  2008 Oct;23(5):916-919. 10.3346/jkms.2008.23.5.916.

Complete Remission of Unresectable Colon Cancer after Preoperative Chemotherapy Selected by Adenosine Triphosphate-Based Chemotherapy Response Assay

Affiliations
  • 1Department of Surgery, Yongdong Severance Hospital, Yonsei University Health System, Seoul, Korea. sksohn@yuhs.ac
  • 2Department of Pathology, Yongdong Severance Hospital, Yonsei University Health System, Seoul, Korea.

Abstract

The adenosine triphosphate-based chemotherapy response assay (ATP-CRA) is a chemosensitivity test that offers the potential of selecting cancer treatments based on the responsiveness of individual tumors. We report a case of 47-yr-old male, presented with sigmoid colon cancer with multiple liver and peritoneal metastases, in which there was a complete response for the primary colon cancer after administration of preoperative chemotherapy selected by ATP-CRA. Oxaliplatin was the most sensitive drug based on the ATP-CRA where the specimen obtained by ultrasound- guided percutaneous liver biopsy was used. After twelve cycles of oxaliplatincapecitabine chemotherapy, abdominopelvic computed tomography revealed marked shrinkage of the liver metastases and positron emission tomography showed no uptake of (18)F-fluoro-deoxy-glucose (FDG) either in the liver or peritoneum except localized uptake in the sigmoid colon. The patient underwent an anterior resection and radiofrequency ablation of the liver metastases, which resulted in a macroscopic curative resection of the cancer cells. Histological examination revealed no residual cancer cells in the resected specimen of the sigmoid colon. This result suggested that preoperative chemotherapy chosen by ATP-CRA may be useful for treating advanced colon cancer with unresectable liver and peritoneal metastases.

Keyword

Adenosine Triphosphate; Drug Screening Assays, Antitumor; Colonic Neoplasms; Complete Remission

MeSH Terms

Adenosine Triphosphate/*metabolism
Antineoplastic Agents/*pharmacology
Antineoplastic Combined Chemotherapy Protocols/therapeutic use
Colonic Neoplasms/*diagnosis/*drug therapy
Deoxycytidine/administration & dosage/analogs & derivatives
Fluorouracil/administration & dosage/analogs & derivatives
Humans
Liver Neoplasms/drug therapy/secondary
Male
Medical Oncology/methods
Middle Aged
Neoplasm Metastasis
Organoplatinum Compounds/administration & dosage
Positron-Emission Tomography
Remission Induction
Treatment Outcome

Figure

  • Fig. 1 Multiple liver metastases in sigmoid colon cancer. (A) Before chemotherapy. (B) After chemotherapy.

  • Fig. 2 Primary sigmoid colon cancer. (A) Before chemotherapy, an exophytic tumor mass (arrow) invading the distal left ureter. (B) After chemotherapy, a slight decrease in the size of the tumor mass (arrow) but no definite interval change. A Hanaro Colorectal Stent® and a double J ureteral stent were visible.

  • Fig. 3 Tumor suppression rate at peak plasma concentration (PPC). Longer bars indicate greater in vitro tumor suppression (p=NS).

  • Fig. 4 After chemotherapy, PET scan showed a localized uptake of 18F-fluoro-deoxy-glucose (FDG) and no uptake in the liver or peritoneum.

  • Fig. 5 Histological features of sigmoid colon cancer. (A) Before chemotherapy, a biopsy of the lesion showed adenocarcinoma (H&E ×200). (B) No residual cancer cells were present in the resected specimen (CR) (H&E ×40).


Cited by  2 articles

Clinical value of an adenosine triphosphate-based chemotherapy response assay in resectable stage III colorectal cancer
Chan Dong Kim, So Hyun Kim, Sang Hoon Jung, Jae Hwang Kim
Ann Surg Treat Res. 2019;97(2):93-102.    doi: 10.4174/astr.2019.97.2.93.

Heterogeneity of Adenosine Triphosphate-Based Chemotherapy Response Assay in Colorectal Cancer - Secondary Publication
Jung Wook Huh, Yoon Ah Park, Kang Young Lee, Seung-Kook Sohn
Yonsei Med J. 2009;50(5):697-703.    doi: 10.3349/ymj.2009.50.5.697.


Reference

1. Adam R, Delvart V, Pascal G, Valeanu A, Castaing D, Azoulay D, Giacchetti S, Paule B, Kunstlinger F, Ghemard O, Levi F, Bismuth H. Rescue surgery for unresectable colorectal liver metastases downstaged by chemotherapy: a model to predict long-term survival. Ann Surg. 2004. 240:644–657.
2. Cortazar P, Johnson BE. Review of the efficacy of individualized chemotherapy selected by in vitro drug sensitivity testing for patients with cancer. J Clin Oncol. 1999. 17:1625–1631.
Article
3. Moon YW, Choi SH, Kim YT, Sohn JH, Chang J, Kim SK, Park MS, Chung KY, Lee HJ, Kim JH. Adenosine triphosphate-based chemotherapy response assay (ATP-CRA)-guided platinum-based 2-drug chemotherapy for unresectable nonsmall-cell lung cancer. Cancer. 2007. 109:1829–1835.
Article
4. Cassidy J, Tabernero J, Twelves C, Brunet R, Butts C, Conroy T, Debraud F, Figer A, Grossmann J, Sawada N, Schoffski P, Sobrero A, Van Cutsem E, Diaz-Rubio E. XELOX (capecitabine plus oxalipatin): active first-line therapy for patients with metastatic colorectal cancer. J Clin Oncol. 2004. 22:2084–2091.
5. Guillem JG, Puig-La Calle J Jr, Akhurst T, Tickoo S, Ruo L, Minsky BD, Gollub MJ, Kilmstra DS, Mazumdar M, Paty PB, Macapinlac H, Yeung H, Saltz L, Finn RD, Erdi Y, Humm J, Cohen AM, Larson S. Prospective assessment of primary rectal cancer response to preoperative radiation and chemotherapy using 18-fluorodeoxyglucose positron emission tomography. Dis Colon Rectum. 2000. 43:18–24.
Article
6. Kaneki T, Koizumi T, Kawashima A, Tsushima K, Kubo K, Fujimoto K, Honda T, Akamatsu T. Double cancer (lung and colon cancer) that showed complete remission with irinotecan and cisplatin combined chemotherapy. J Gastroenterol. 2000. 35:864–869.
Article
7. Brandi G, Pantaleo MA, Calabrese C, Di Battista M, Poggi R, Bajetta E, Biasco G. Complete remission of primary colon cancer in a metastatic patient treated with CPT-11 plus capecitabine. Int J Colorectal Dis. 2004. 19:599–602.
Article
8. Huh JW, Park YA, Sohn SK, Choi SH. In-vitro chemosensitivity test for colorectal cancer using an adenosine-triphosphate-based chemotherapy response assay (ATP-CRA). J Korean Soc Coloproctol. 2007. 23:172–179.
Article
9. Meta-analysis Group in Cancer. Efficacy of intravenous continuous infusion of fluorouracil compared with bolus administration in advanced colorectal cancer. J Clin Oncol. 1998. 16:301–308.
10. Goldberg RM, Sargent DJ, Morton RF, Fuchs CS, Ramanathan RK, Williamson SK, Findlay BP, Pitot HC, Alberts SR. A randomized controlled trial of fluorouracil plus leucovorin, irinotecan, and oxaliplatin combinations in patients with previously untreated metastatic colorectal cancer. J Clin Oncol. 2004. 22:23–30.
Article
11. Tournigand C, Andre T, Achille E, Lledo G, Flesh M, Mery-Mignard D, Quinaux E, Couteau C, Buyse M, Ganem G, Landi B, Colin P, Louvet C, de Gramont A. FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol. 2004. 22:229–237.
Article
12. Schrag D, Garewal HS, Burstein HJ, Samson DJ, Von Hoff DD, Somerfield MR. American Society of Clinical Oncology Technology Assessment: chemotherapy sensitivity and resistance assays. J Clin Oncol. 2004. 22:3631–3638.
Article
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