# Prospective clinical study of R-CMD therapy for indolent B cell lymphoma and mantle cell lymphoma from the Hokuriku Hematology Oncology Study Group

**Authors:** Tomoyuki Sakai, Yasufumi Masaki, Nozomi Otsuki, Ippei Sakamaki, Shinji Kishi, Takayoshi Miyazono, Yoshimasa Urasaki, Jun Murakami, Tomomi Satoh, Takuji Nakamura, Haruka Iwao, Akio Nakajima, Takafumi Kawanami, Miyuki Miki, Yoshimasa Fujita, Masao Tanaka, Toshihiro Fukushima, Toshiro Okazaki, Takanori Ueda

PMC · DOI: 10.1007/s12032-015-0677-9 · Medical Oncology (Northwood, London, England) · 2015-08-15

## TL;DR

This study evaluated the effectiveness and safety of R-CMD therapy for treating indolent B cell lymphoma and mantle cell lymphoma, showing promising results with high response rates.

## Contribution

The study provides new evidence on the efficacy of R-CMD therapy for indolent B cell lymphoma and mantle cell lymphoma in a prospective clinical setting.

## Key findings

- 26 out of 33 patients achieved complete or unconfirmed complete response to R-CMD therapy.
- R-CMD therapy was found to be relatively convenient and effective for treating indolent B cell lymphoma and mantle cell lymphoma.
- Four patients relapsed after remission, highlighting the need for continued monitoring and infection prevention.

## Abstract

Standardized treatments for indolent B cell lymphoma primarily consisting of follicular lymphoma (FL) and for mantle cell lymphoma (MCL) have yet to be established. Here the Hokuriku Hematology Oncology Study Group conducted a multicenter prospective study to investigate the efficacy and safety of a combination regimen of rituximab, cladribine, mitoxantrone, and dexamethasone (R-CMD) in indolent B cell lymphoma and MCL. A total of 33 CD20-positive patients who received care between January 2008 and August 2011 were investigated. These patients’ illnesses were FL (n = 21), nodal marginal zone B cell lymphoma (NMZB, n = 3), MCL (n = 3), splenic marginal zone B cell lymphoma (n = 2), hairy cell leukemia (n = 1), Waldenstrom macroglobulinemia (WM, n = 1), and lymphoplasmacytic lymphoma (LPL, n = 2). Patients received four 21-day cycles of rituximab 375 mg/m2 (day 1), cladribine 0.10 mg/kg (days 1–3), mitoxantrone 8 mg/m2 (day 1), and dexamethasone 8 mg/body (days 1–3), with four additional rituximab doses at 4-week intervals. Of the 33 patients, 26 achieved complete response/unconfirmed complete response, and six achieved a partial response (4 with FL, 1 with NMZB, 1 with WM). One had progressive disease (FL), and four relapsed after remission (1 with FL, 2 with MCL, 1 with LPL). R-CMD therapy was relatively convenient and effective in indolent B cell lymphoma and MCL. Nonetheless, to suppress the number and function of both B cells and T cells, comprehensive infection prevention and follow-up are necessary in the future.

## Linked entities

- **Chemicals:** cladribine (PubChem CID 20279), mitoxantrone (PubChem CID 4212), dexamethasone (PubChem CID 5743)
- **Diseases:** indolent B cell lymphoma (MONDO:0017594), mantle cell lymphoma (MONDO:0018876), follicular lymphoma (MONDO:0018906), nodal marginal zone B cell lymphoma (MONDO:0019465), splenic marginal zone B cell lymphoma (MONDO:0019462), hairy cell leukemia (MONDO:0018935), Waldenstrom macroglobulinemia (MONDO:0100280), lymphoplasmacytic lymphoma (MONDO:0000432)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, ADA (adenosine deaminase) [NCBI Gene 100] {aka ADA1}, KRT88P (keratin 88, pseudogene) [NCBI Gene 85348] {aka HBC, KRT122P, KRTHBP3}
- **Diseases:** bacterial fasciitis (MESH:D005208), Alopecia (MESH:D000505), myelodysplastic syndrome (MESH:D009190), LPL (MESH:D008223), Lymphopenia (MESH:D008231), leukemia (MESH:D007938), Hairy cell leukemia 1 (MESH:D007943), pneumocystis pneumonia (MESH:D011020), urinary tract infection (MESH:D014552), hand stiffness (MESH:C566112), herpes labialis (MESH:D006560), pancreatic cancer (MESH:D010190), influenza (MESH:D007251), Infusion-related reaction (MESH:D000075662), cancers (MESH:D009369), herpes zoster (MESH:D006562), Hematological    Leukopenia (MESH:D007970), LPL (MESH:D008072), sepsis (MESH:D018805), WM (MESH:D008258), cirrhosis type C (MESH:D005355), FPD-R (MESH:C563324), Constipation (MESH:D003248), mycosis (MESH:D015821), hematological toxicity (MESH:D006402), Thrombocytopenia (MESH:D013921), TTP (MESH:D011697), pyothorax (MESH:D016724), weight loss (MESH:D015431), fever (MESH:D005334), FL (MESH:D008224), FMD (MESH:C536391), B cell lymphoma (MESH:D016393), NHL (MESH:D008228), Neutropenia (MESH:D009503), necrotizing bacterial fasciitis (MESH:D019115), MALT lymphoma (MESH:D018442), Oncology (MESH:D000072716), CR (MESH:D001766), CMD (MESH:C565145), Infections (MESH:D007239), FND (MESH:C563177), small lymphocytic lymphoma (MESH:D015451), Anemia (MESH:D000740), Rash (MESH:D005076), marginal-cell lymphoma (MESH:D016399), PR (MESH:D004828), pneumocystis infection (MESH:D016720), B symptoms (MESH:D006509), Toxicity (MESH:D064420), liver cancer (MESH:D006528), death (MESH:D003643), PD (MESH:D018450), MCL (MESH:D020522)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human T-cell leukemia virus type I (no rank) [taxon 11908], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC4537487/full.md

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Source: https://tomesphere.com/paper/PMC4537487