Prospective Multicenter Study of the Impact of Oncotype DX Colon Cancer Assay Results on Treatment Recommendations in Stage II Colon Cancer Patients

Author:

Srivastava Geetika1,Renfro Lindsay A.1,Behrens Robert J.2,Lopatin Margarita3,Chao Calvin3,Soori Gamini S.4,Dakhil Shaker R.5,Mowat Rex B.6,Kuebler J. Philip7,Kim George8,Mazurczak Miroslaw9,Lee Mark3,Alberts Steven R.1

Affiliation:

1. Mayo Clinic, Rochester, Minnesota, USA

2. Medical Oncology and Hematology Associates, Des Moines, Iowa, USA;

3. Genomic Health, Inc., Redwood City, California, USA;

4. Alegent Bergan Mercy Cancer Center, Omaha, Nebraska, USA;

5. Cancer Center of Kansas, Wichita, Kansas, USA;

6. Toledo Clinic, Toledo, Ohio, USA;

7. Columbus Oncology Associates, Columbus, Ohio, USA;

8. Mayo Clinic, Jacksonville, Florida, USA;

9. Sanford Hospital, Sioux Falls, South Dakota, USA

Abstract

Abstract Purpose. The Oncotype DX colon cancer assay is a clinically validated predictor of recurrence risk in stage II colon cancer patients. This prospective study evaluated the impact of recurrence score (RS) results on physician recommendations regarding adjuvant chemotherapy in T3, mismatch repair-proficient (MMR-P) stage II colon cancer patients. Patients and Methods. Stage IIA colon cancer patients were enrolled in 17 centers. Patient tumor specimens were assessed by the RS test (quantitative reverse transcription-polymerase chain reaction) and mismatch repair (immunohistochemistry). For each patient, the physician's recommended postoperative treatment plan of observation, fluoropyrimidine monotherapy, or combination therapy with oxaliplatin was recorded before and after the RS and mismatch repair results were provided. Results. Of 221 enrolled patients, 141 patients had T3 MMR-P tumors and were eligible for the primary analysis. Treatment recommendations changed for 63 (45%; 95% confidence interval: 36%–53%) of these 141 T3 MMR-P patients, with intensity decreasing for 47 (33%) and increasing for 16 (11%). Recommendations for chemotherapy decreased from 73 patients (52%) to 42 (30%), following review of RS results by physician and patient. Increased treatment intensity was more often observed at higher RS values, and decreased intensity was observed at lower values (p = .011). Conclusion. Compared with traditional clinicopathological assessment, incorporation of the RS result into clinical decision making was associated with treatment recommendation changes for 45% of T3 MMR-P stage II colon cancer patients in this prospective multicenter study. Use of the RS assay may lead to overall reduction in adjuvant chemotherapy use in this subgroup of stage II colon cancer patients.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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