Seth Tulika, Melinkeri Sameer, Dolai Tuphan Kanti, Bhattacharyya Jina, Sidharthan Neeraj, Chakrabarti Prantar, Malalur Chaithanya, Taur Santosh
Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Department of Hematology, Deenanath Mangeshkar Hospital, Pune, India.
Front Oncol. 2025 May 1;15:1546641. doi: 10.3389/fonc.2025.1546641. eCollection 2025.
Individuals with hematological malignancies (HMs) are at a high risk of invasive pneumococcal disease due to underlying malignancy and subsequent immunosuppressive anticancer therapy. Early management of pneumococcal infections is crucial for reducing morbidity and mortality in this vulnerable patient subgroup. In this study, we aim to review the current evidence and recommendations regarding the use of pneumococcal conjugate vaccines (PCVs) in patients with HMs and develop a consensus document on the optimal timing and patient profiles who can benefit from them.
The modified Delphi consensus method was used for achieving consensus. The panel comprised a scientific committee of six experts from India. Questions were drafted for discussion around: (i) the risk and consequences of pneumococcal disease in HMs; (ii) barriers to pneumococcal vaccination in the hemato-oncology clinical setting; and (iii) evidence and optimal timing of pneumococcal vaccines in HMs. The questionnaire was shared with the panel through an online survey platform (Delphi round 1). The consensus level was classified as high (≥80%), moderate (60%-79%), and low (< 60%). A Delphi round 2 meeting was conducted to discuss the questions that received near or no consensus to reach an agreement. The final draft of consensus statements was circulated among the experts for approval.
Pneumonia with or without bacteremia and bacteremia without foci of infection are the most frequently reported clinical presentations of pneumococcal infections in patients with HMs. A high risk of pneumococcal disease has been observed in patients with multiple myeloma (MM), acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), and chronic lymphocytic leukemia (CLL). Priming with PCV enhances the response to pneumococcal polysaccharide vaccine 23 (PPSV23) in patients with HMs. Experts agreed that PCV is beneficial and can be strongly recommended in patients with CLL, MM, and patients undergoing hematopoietic stem cell transplantation. Children with acute lymphoblastic leukemia (ALL) would benefit from systematic revaccination with PCV after chemotherapy. The evidence is inadequate to consistently recommend pneumococcal vaccination to all patients with lymphoma, AML, and adults with ALL.
This expert consensus will guide clinicians on the recommended approach for administering pneumococcal vaccination to patients with HMs.
血液系统恶性肿瘤(HM)患者由于潜在的恶性肿瘤及后续的免疫抑制抗癌治疗,发生侵袭性肺炎球菌疾病的风险很高。肺炎球菌感染的早期管理对于降低这一脆弱患者亚组的发病率和死亡率至关重要。在本研究中,我们旨在回顾关于血液系统恶性肿瘤患者使用肺炎球菌结合疫苗(PCV)的现有证据和建议,并就最佳接种时机以及能从中受益的患者特征制定一份共识文件。
采用改良的德尔菲共识方法达成共识。该小组由来自印度的六位专家组成的科学委员会构成。围绕以下方面起草问题以供讨论:(i)血液系统恶性肿瘤患者肺炎球菌疾病的风险和后果;(ii)血液肿瘤临床环境中肺炎球菌疫苗接种的障碍;(iii)血液系统恶性肿瘤患者肺炎球菌疫苗的证据和最佳接种时机。通过在线调查平台(第一轮德尔菲法)向小组成员发放问卷。共识水平分为高(≥80%)、中(60%-79%)和低(<60%)。召开第二轮德尔菲会议,讨论那些接近或未达成共识的问题以达成一致意见。将共识声明的最终草案分发给专家们进行审批。
伴有或不伴有菌血症的肺炎以及无感染灶的菌血症是血液系统恶性肿瘤患者中最常报告的肺炎球菌感染临床表现。在多发性骨髓瘤(MM)、急性髓系白血病(AML)、急性淋巴细胞白血病(ALL)和慢性淋巴细胞白血病(CLL)患者中观察到肺炎球菌疾病的高风险。用PCV进行初始接种可增强血液系统恶性肿瘤患者对肺炎球菌多糖疫苗23(PPSV23)的反应。专家们一致认为,PCV有益,强烈推荐给CLL、MM患者以及接受造血干细胞移植的患者。急性淋巴细胞白血病(ALL)儿童在化疗后进行PCV系统再接种将受益。证据不足,无法始终如一地向所有淋巴瘤、AML患者以及成年ALL患者推荐肺炎球菌疫苗接种。
这一专家共识将指导临床医生对血液系统恶性肿瘤患者进行肺炎球菌疫苗接种的推荐方法。