Real-World Challenges of Managing Diffuse Large B-Cell Lymphoma in a Developing Country

Author:

Iftikhar Raheel1ORCID,Ahmad Usman2,Haider Ghulam3,Mahmood Humera4,Khan Maryam1,Masood Misbah5,Anwar Nida6,Javed Qamar7,Sajid Nadia5,Tariq Rija5,Mehmod Sana4,Haider Javeria4,Abro Nargis Aalam3,Shahbaz Shanzah8,Khokhar Abbas9,Khan Zeeshan Ahmed10,Pervez Hassan11,Moosajee Munira12ORCID,Aziz Zeba10ORCID

Affiliation:

1. Armed Forces Bone Marrow Transplant Center, Rawalpindi, Pakistan

2. Shoukat Khanam Memorial Cancer Hospital and Research Center, Lahore, Pakistan

3. Jinnah Post Graduate Medical Centre, Karachi, Pakistan

4. Nuclear Medicine, Oncology and Radiotherapy Institute, Rawalpindi, Pakistan

5. Institute of Nuclear Medicine and Oncology, Lahore, Pakistan

6. National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, Pakistan

7. PINUM Cancer Hospital, Faisalabad, Pakistan

8. Sheikh Zayed Medical College and Hospital, Rahim Yar Khan, Pakistan

9. Mayo Hospital, Lahore, Pakistan

10. Hameed Latif Hospital, Lahore, Pakistan

11. National Hospital, Lahore, Pakistan

12. Aga Khan University Hospital, Karachi, Pakistan

Abstract

PURPOSE To highlight challenges and cancer care disparities in patients of diffuse large B-cell lymphoma management in resource-constrained settings. MATERIALS AND METHODS This multicenter retrospective study included 738 patients from 12 public and private sector hematology-oncology centers across Pakistan. Patients were divided into limited-resource and enhanced-resource settings as per national diffuse large B-cell lymphoma (DLBCL) guidelines. RESULTS The median age at diagnosis was 47 years (range, 14-89). Male:female ratio was 2.5:1. Majority of the patients (69.3%) were treated in limited-resource settings. Computed tomography was used as a staging modality in 442 (60%) patients. Limited-stage DLBCL was present in 13.5% of patients, while 86.3% had advanced-stage disease at diagnosis. First-line regimens included rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone in 56% and cyclophosphamide, doxorubicin, vincristine, prednisone in 34% of patients, while 10% of patients received palliative regimens upfront. Of evaluable data, complete remission was documented in 299 (74.4%) patients, 39 (9.8%) had partial response and 63 (13.5%) had progressive disease. Disease-free survival (DFS) and overall survival (OS) status were not available for 345 (46.8%) patients at the time of data collection. Overall study cohort had a median follow-up of 2.2 years with a median OS of 3.6 years (95% CI, 3.1 to 4.1), median DFS of 3.1 years (95% CI, 2.6 to 3.6), and a 5-year OS of 40% and DFS of 36%. CONCLUSION Patients from low- and middle-income countries present at an earlier age and have more advanced disease. Patients were frequently lost to follow-up, and record keeping was inadequate more so in patients treated in limited-resource settings. There is a need to establish a national lymphoma registry, improve record keeping, and standardize treatments to ensure improvement in treatment outcomes.

Publisher

American Society of Clinical Oncology (ASCO)

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