Long-term survival of gastrointestinal cancer diagnosed in Hodgkin lymphoma survivors.

Authors

null

Lisanne Sara Rigter

The Netherlands Cancer Institute, Amsterdam, Netherlands

Lisanne Sara Rigter , Michael Schaapveld , Berthe M.P. Aleman , Cecile P.M. Janus , Anna M. van Eggermond , Augustinus D.G. Krol , Richard Van Der Maazen , Judith M. Roesink , Josee M Zijlstra , Gustaaf Willem Van Imhoff , Philip M. Poortmans , Max Beijert , Pieternella J. Lugtenburg , Otto Visser , Petur Snaebjornsson , Flora Van Leeuwen , Monique Esther van Leerdam

Organizations

The Netherlands Cancer Institute, Amsterdam, Netherlands, Department of Psychosocial Oncology and Epidemiology, The Netherlands Cancer Institute, Amsterdam, Netherlands, Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands, Erasmus Medical Center Cancer Institute, Department of Radiation Oncology, Rotterdam, Netherlands, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, Netherlands, Leiden University Medical Center, Department of Clinical Oncology, Leiden, Netherlands, Radboud University Medical Center, Nijmegen, Netherlands, Department of Radiotherapy, University Medical Center Utrecht, Utrecht, Netherlands, Department of Hematology, VU University Medical Center, Amsterdam, Netherlands, Univ Medical Center Groningen, Groningen, Netherlands, Radiation Oncology Department, Radboud University Medical Centre Nijmegen, Nijmegen, Netherlands, University Medical Center Groningen, Groningen, Netherlands, Department of Hematology, Erasmus MC Cancer Insitute, Rotterdam, Netherlands, Comprehensive Cancer Centre the Netherlands, Utrecht, Netherlands

Research Funding

Other

Background: The risk of developing gastrointestinal (GI) cancer is increased in Hodgkin lymphoma survivors. This study aims to compare overall survival of GI cancer in Hodgkin lymphoma survivors with survival of first primary GI cancer patients. Methods: This cohort study compared overall survival of GI cancer patients in a Hodgkin lymphoma survivor population (HL-GI (n = 92) including esophageal (n = 25), gastric (n = 31), small intestinal (n = 2), colorectal cancer (n = 34)) with survival of a population-based cohort of first primary GI cancer patients (GI-1, n = 911) which was generated by individual matching of the 92 cases, based on tumor location, gender, age and year at diagnosis. Clinical characteristics were compared by Chi square tests. Cox regression was used for multivariable survival analysis (corrected for age, gender, and clinicopathological characteristics related to the GI tumor). Results: When comparing HL-GI and GI-1 patients, no differences in tumor stage, grade of differentiation or frequency of surgery were found. HL-GI patients were less frequently treated for their GI tumor with radiation therapy (7% vs. 24% in GI-1 patients, p < 0.001) or chemotherapy (28% vs. 41%, p = 0.02). Overall 5-year and 20-year survival of HL-GI patients and GI-1 patients was non-significantly lower (28% vs. 38%, p = 0.13 and 19% vs. 29%, p = 0.06, respectively). This result was confirmed multivariably (5-year survival, p = 0.33, 20-year survival, p = 0.14). Also, for esophageal, gastric and colorectal cancer separately, no differences in overall survival were found between HL-GI patients and GI-1 patients. Conclusions: Long-term overall survival of GI cancer patients is similar in Hodgkin lymphoma survivors and first primary GI cancer patients. HL-GI patients did however receive less treatment with radiation therapy or chemotherapy. These treatments may not have been recommended due to prior Hodgkin lymphoma treatment or comorbidity. As risks of other causes of mortality are also increased in Hodgkin lymphoma survivors, the relatively good survival in this population is remarkable.

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Abstract Details

Meeting

2017 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Cancers of the Esophagus and Stomach

Track

Cancers of the Esophagus and Stomach

Sub Track

Prevention, Diagnosis, and Screening

Citation

J Clin Oncol 35, 2017 (suppl 4S; abstract 40)

DOI

10.1200/JCO.2017.35.4_suppl.40

Abstract #

40

Poster Bd #

E18

Abstract Disclosures