Hypoxia modulation vs. chemotherapy and tumor shrinkage on early response assessment in diffuse large B-cell lymphoma

  • Ridho M. Naibaho Abdoel Wahab Sjahranie http://orcid.org/0000-0002-9777-9705
  • Eko Pangarsa Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Kariadi Hospital, Faculty of Medicine Diponegoro University, Semarang, Indonesia
  • Daniel Rizky Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Kariadi Hospital, Faculty of Medicine Diponegoro University, Semarang, Indonesia
  • Sigit P. Kurniawan Department of Hematology/Medical Oncology, Department of Internal Medicine, Lambung Mangkurat University/Ulin General Hospital, Banjarmasin, and Hadji Boejasin General Hospital, Tanah Laut, Indonesia
  • Hermawan Istiadi Department of Anatomical Pathology, Dr Kariadi Hospital, Semarang, Indonesia
  • Dik Puspasari Department of Anatomical Pathology, Dr Kariadi Hospital, Semarang, Indonesia
  • Gunawan Santoso Department of Radiology, Faculty of Medicine Diponegoro University, Dr. Kariadi General Hospital, Semarang, Indonesia
  • Damai Santosa Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Kariadi Hospital, Faculty of Medicine Diponegoro University, Semarang, Indonesia
  • Budi Setiawan Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Kariadi Hospital, Faculty of Medicine Diponegoro University, Semarang, Indonesia
  • Catharina Suharti Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Kariadi Hospital, Faculty of Medicine Diponegoro University, Semarang, Indonesia
Keywords: Hypoxia modulation, lactate, tumor volume, diffuse large B-cell lymphoma

Abstract


Background: Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) chemotherapy remains the standard of first-line treatment for diffuse large B-cell lymphoma (DLBCL). Up to 40% of DLBCL is characterized by relapse and refractory after treatment. Preliminary study reported Hypoxia-inducible factor-1  (HIF-1 ) overexpression in 88.5% of DLBCL tumors in the Dr. Kariadi Hospital. Moreover, the role of hypoxia and HIF-1  has previously never been explored in DLBCL.

Objectives: To evaluate the effect of hypoxia modulation to increased chemotherapeutic response in DLBCL.

Methods: Single blind randomized control study was performed, with pre-test and post-test control group design.

 Research sampling consisted of DLBCL patients. The inclusion criteria include newly diagnosed DLBCL with HIF-1  overexpression and randomized to receive hypoxia modulation consisting of carbogen inhalation and nicotinamide administration, before R-CHOP chemotherapy. The tissue biopsy, histopathology and immunohistochemical studies were done. Chemotherapeutic responses were evaluated after 10-14 days following the first cycle of R-CHOP chemotherapy.

Results: Out of twenty-six DLBCL participants with HIF-1  overexpression, there were 20 participants who completed the research protocol: 10 participants each in the intervention and control group. Demographic, clinicopathological, laboratory and disease characteristics were not statistically different between the two research groups (p>0.05). Baseline tumor volume to be evaluated was also considered equal (172.3 cm3 vs. 152.8 cm3, p=0.597). Following the carbogen inhalation and nicotinamide administration, serum HIF-1  and lactate reduction can be observed. There was also a significant tumor volume shrinkage in both the intervention and control (mean –85.7 cm3 vs. –118.27 cm3) group, though the reduction was not statistically different (Delta 58.85% vs. 65.63%, p=0.474).

 

Conclusion: The addition of hypoxia modulation to R-CHOP chemotherapy for DLBCL has shown beneficial effects on both serum HIF-1  and lactate concentration. However, the benefits did not correlate to increase a better tumor response compared to the control group.

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Published
2024/08/13
Section
Original Scientific Paper