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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1175633 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
1 i+ S0 G' j$ Y: t$ lNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 $ w; y6 p* w" j3 n1 ^! g. B
+ Author Affiliations3 N1 ?% d, M# {, j# Q* U
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
: ]* N) J) X$ S2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 Y; @6 S: q% Y. X/ D2 \3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
# {5 j+ l8 |' C" z2 ~; D3 n; `& o, L4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
3 C& A& E9 x( }5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! }- B  U/ s: Y2 f4 w8 ^; @3 X+ _% H2 Y
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 8 A# D1 y* K& X6 C+ e2 E% X
7Kinki University School of Medicine, Osaka 589-8511, Japan
4 ]3 u0 @  H5 h( C  s( L/ c8Izumi Municipal Hospital, Osaka 594-0071, Japan + Y7 H3 H6 e3 {# v  L% Q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
% P- s- G* E' C2 I! bCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp & p( j2 o3 v! N
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. " P, M$ K  R9 ~8 p8 l) m

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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$ P2 Y" x, f4 b1 GAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . P2 z& q+ E* n! q6 ^) J( [4 |

6 F2 F# g4 I( S" Z/ uAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
6 O! }! o2 w2 S6 {7 [; }' c# |/ D. n
Published online on: Thursday, December 1, 2011
) i+ Q4 ]; k/ e; o  t
  {) K& f8 Q% h9 q* ^) HDoi: 10.3892/ol.2011.507
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$ _/ e! j9 M1 h1 rPages: 405-410
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  P/ d  U/ q* \Abstract:5 M4 B" L) W6 Y1 C" Q' A- p
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.1 q$ n. x! g# x7 L

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
% ?& A. q* x6 {F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
' X0 T0 a+ V6 a1 d5 L1 m+ Author Affiliations
- f% M2 ]7 a  U% ]* I1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
$ s/ z# d) }. {# o% P2Department of Thoracic Surgery, Kyoto University, Kyoto
" t6 d% ~( k3 D2 ^3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ) h& ^9 X+ @7 Q2 T$ j1 y* Z
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
8 _# \2 P' [2 V+ A& FReceived September 3, 2010.
5 V, J/ B. O% i" aRevision received November 11, 2010. 9 F" m; `6 D) [
Accepted November 17, 2010.
) H; D& V$ Y5 w* n4 RAbstract
. l( O9 W' H4 c/ J; tBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. 1 P3 e7 u# \. t8 E0 v4 }
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 4 ~2 b1 j% G" k) j- z: U
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
# L: Y3 R% U+ ]- }/ d! z; V8 n# J/ TConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. / Q4 A9 ?( W# W0 R1 n& D
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
1 ?" W; W) J1 ^( x/ C" F# l6 G今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?# \( V; l) t2 s4 [
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy7 B3 A% ~. P# a* g" l% B" t
http://clinicaltrials.gov/ct2/show/NCT01523587  Y1 N  P2 d# d0 J
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# ~4 Q& @2 ], c/ V1 H% shttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 & S* i& g; {3 |# d3 i8 F9 u
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。: {. t) i6 g- }
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
! F2 v" x: g4 j) h  n从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
2 d& q5 X  M) a: @$ Q, R' V9 N至今为止,未出 ...

% C1 D) s9 z. s. u没有副作用是第一追求,效果显著是第二追求。
8 Q- U8 V9 m8 z& C0 o不错。

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